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I had $150 in my trading account last Thursday or Friday and decided to
throw it away on 20 $18 calls just in case news came out. I got them for .07 and they are now selling at $1.15.
Major dilemma whether to sell now or hold until Friday's expiration.
My only day off is today, so decision time before the close I guess.
--------------------
This will take us to a whole new level
Funds loading up
We will see some price target updates next few days
This will take us to a whole new level
Funds loading up
We will see some price target updates next few days
BOOM
FDA Grants Breakthrough Therapy Designation to Omeros’ MASP-2 Inhibitor OMS721 for the Treatment of IgA Nephropathy
FDA Grants Breakthrough Therapy Designation to Omeros’ MASP-2 Inhibitor OMS721 for the Treatment of IgA Nephropathy
Yee hah
-------------------
Doc,
thanks did not know about shareholder meeting
I am gathering some funds.
snup
And shareholders meeting friday, if you look at price action yesterday,guess investors think ceo will end meeting like steve jobs did with his ipod LOL
Doc,
in retrospect I wish I had sold eltp but am stuck , but bios as you
know are un-predictable so I continue to lie in da bed created.
fins will not be pretty but at this point short term it is all
about sequest.
positive motley fool blurb on omer last week
snup
Was elites milestone payment of $5m a year ago on next financials?
If so YOY growth numbers wont be impressive.
Also the rest of the numbers wont be much to cheer at too i guess. I mean its been around 2 mil a Q for a few years now, with 12 or 14 products in different strenghts thats about a stable 100k per product.
A return to the 30 is still far away i guess,that would bring them at a vallue of 60% of omeros market cap.
Outstanding shares close to 1 billion ruined it imo.
I would say sell the next time it reach $0.24 and trade it at 18 or 19
And dont await approval all in, another failure will have you lockef down another year, if granted you can always jump after opening with 20% less profit wich is nothing in the long run after approval
I will be happy to jump back all in at a higher price for a guaranteed profit ,than to risk another year of beeing locked down. Just my opinion
Have a good week snup.
oops,
super glued in the low 30's with majority position
which I will hold thru sequestox glory and buy out in
a year or two but who knows ? maybe in july partner?
snup
Hi Doc,
Looking to exit ptie this week 10+k before tax man much needed
for hse hold needs.4's ? how about that
still watching omer for entry for a couple of k shares
elite fins due. would very much like return to 30's as I need
to unload shares in the teens-20s have to many.
make it a great week
snup
Doc,
My 3 day hold period is up with ptie,
I have not yet, but will flip it near
term Just think it will go back to 4
in short term, about 10k for me.
omer is a buy and hold kind of stock so
I need time coin to do it. remain all in
on eltp and some with a few others.
snup
Doc,
thanks will read about progenics pharm.
You know bios better than I , they can be the
same exact company one month from the next six months yet trade
at wild variations. I think you will get some restaurant/uber/
tip monies from your trade. I am handcuffed with eltp, over
extended, averaged down to many times from my majority at
30-34 cent range but as I take some off the table I will position
for a long term hold with omer,
make it a great week, I no longer am able to work but always enjoyed
it.
snup
Gonna buy 3k ptie today, see how it turns out. Also keep an eye on pgnx
Chart is ready to bounce too, pretty strong fundamentals to trade around current low prices
Gltu
Doc,
bounce play, no news coming for a while.
keeping an eye on omer
snup
Thats a large number of ptie shares
Bounce play or upcoming catalyst i dont know of
Today Omer presenting OMS721 data before 7000 international physicians and potential euro partners in spain.
Lets hope some of them speculate on the stock market
Thanks, I read that site often.
Hi Doc,
well ptie down to my buy price picked up 19.5k today
some below 3.50
still watching omer, enjoy your weekend
snup
I told you they have submitted the breakthrough application over a month ago , but i just see it only 3 weeks ago.
He announced it during Q1 CC
Come over to stocktwits, much more DD to be found than here on ihub
Thanks, looks like there is a 60 day review for those filings.
Yes, they have submitted the breakthrough application over a month ago
Could be granted any week now
Gltu
Did OMER apply for Breakthrough Designation yet?
If they did, I can't find it.
Please prove me wrong so I can go all in.
--------------------
Glyc up over 100% on Breakthrough Therapy Designation status, omeros could be granted Breakthrough Therapy Designation status within few weeks based on PR
maiby next dip you can buy a few shares to see how it plays out.
GL
Doc,
possibly thanks for advise
snup
Glyc up over 100% on Breakthrough Therapy Designation status, omeros could be granted Breakthrough Therapy Designation status within few weeks based on PR
maiby next dip you can buy a few shares to see how it plays out.
GL
Doc,
congrats! I'm pleased for you, omer has a lot of staying power!
snup
Omeros Announces Completion of IgA Nephropathy Cohort in OMS721 Phase 2 Clinical Trial
Source: Business Wire
-- Additional Positive Results Support Rapid Advancement to Phase 3 Trial --
Omeros Corporation (NASDAQ: OMER) today announced completion of the IgA nephropathy cohort and reported additional positive results from the first stage of the company’s Phase 2 clinical trial of OMS721 for the treatment of serious kidney disorders. All patients in the cohort have now completed the OMS721 treatment and follow-up periods. The additional Phase 2 results in IgA nephropathy patients expand on the data reported earlier this year and further demonstrate marked and statistically significant improvement in urine protein levels (proteinuria). Proteinuria reduction is associated with slowing progression of kidney functional loss, and greater proteinuria reductions are associated with progressively better prognoses. OMS721 is Omeros’ lead human monoclonal antibody targeting mannan-binding lectin-associated serine protease-2 (MASP-2), the effector enzyme of the complement system’s lectin pathway.
“I have never seen the clinical responses that I’ve observed in IgA nephropathy patients treated with OMS721,” stated Geoffrey Block, M.D., Director of Clinical Research at Denver Nephrology and Principal Investigator of the trial. “All of these patients had significant renal impairment when they entered the trial and each patient dramatically improved. The improvements in these patients continued to increase after the end of treatment and persisted following completion of the trial. As an active clinical investigator, given the strength of these data, I am working hard to move this promising drug through the clinical trial process.”
The first stage in this Phase 2 trial includes four different types of complement-associated kidney diseases: IgA nephropathy, membranous nephropathy, lupus nephritis, and complement component 3 (C3) glomerulopathy. All patients had pre-existing renal impairment. To meet enrollment criteria, patients must have high levels of proteinuria despite well-controlled blood pressure with stable dosing of renin-angiotensin system inhibitors and ongoing (at least three months) corticosteroid treatment prior to receiving OMS721. Patients in this cohort are treated open-label with OMS721 for a total of 12 weeks and then followed post-treatment for six weeks. The trial endpoints are measured throughout the treatment and follow-up periods and assess the effect of OMS721 on urine protein measures that are predictive of kidney failure, namely urine albumin-to-creatinine ratio (uACR) and total 24-hour urine protein excretion.
All IgA nephropathy patients had Stage 3B chronic kidney disease and three of the four patients had nephrotic range proteinuria. All patients demonstrated marked improvement in uACRs and in 24-hour urine protein excretion while concurrently tapering corticosteroid treatment. The mean baseline uACR in these patients was 1,457 mg/g and reached 332 mg/g at the end of the follow-up period (77 percent decrease; p = 0.026). One patient’s uACR normalized by the National Kidney Foundation criterion. Results of 24-hour urine protein excretion were highly consistent with the uACR results, with a reduction from a mean of 3,935 mg/day at baseline to a mean of 1,067 mg/day at the end of the follow-up period (73 percent decrease; p = 0.013). All patients achieved partial remission based on proteinuria and one patient with nephrotic range proteinuria achieved a 95 percent reduction, reaching reference laboratory-established normal urine protein levels. All patients also were able to eliminate or greatly reduce their corticosteroid dosing.
“The OMS721 results in patients with IgA nephropathy continue to be striking,” said Jonathan Barratt, Ph.D., F.R.C.P., Professor of Renal Medicine in the Department of Infection, Immunity & Inflammation at University of Leicester and Honorary Consultant Nephrologist at Leicester General Hospital. “The degree of improvement observed with OMS721 is the largest I have seen and I expect will result in significant improvement in renal outcomes.”
Consistent with all other OMS721 clinical trials, no significant safety concerns have been observed. The most commonly reported adverse events in this trial are fatigue and anemia.
“We are pleased with the continued consistency of the results seen in these patients treated with OMS721,” stated Gregory A. Demopulos, M.D., chairman and chief executive officer of Omeros. “Despite being an orphan disease, IgA nephropathy is the most common primary glomerular disease worldwide, and we are keenly focused on this indication for OMS721. We are aggressively advancing to our Phase 3 clinical trial and look forward to beginning patient enrollment as soon as possible.”
No treatments are approved for IgA nephropathy. With an annual incidence of approximately 1 per 100,000, it is estimated that 1 in 1,400 persons in the U.S. will develop IgA nephropathy in his or her lifetime. As many as 40 percent of them will develop end-stage renal disease.
While preparing for its Phase 3 clinical trial in IgA nephropathy, Omeros is continuing to conduct the second stage of its ongoing Phase 2 clinical trial in which OMS721 is evaluated in non-steroid-treated patients with IgA nephropathy. As previously reported, 4 of 5 lupus nephritis patients in the Phase 2 trial also demonstrated marked reduction in 24-hour urine protein levels (mean reduction of 69 percent) with OMS721 treatment. Further analyses are in progress.
About Omeros’ MASP Programs
Omeros controls the worldwide rights to MASP-2 and all therapeutics targeting MASP-2, a novel pro-inflammatory protein target involved in activation of the complement system, which is an important component of the immune system. The complement system plays a role in the inflammatory response and becomes activated as a result of tissue damage or microbial infection. MASP-2 is the effector enzyme of the lectin pathway, one of the principal complement activation pathways. Importantly, inhibition of MASP-2 does not appear to interfere with the antibody-dependent classical complement activation pathway, which is a critical component of the acquired immune response to infection, and its abnormal function is associated with a wide range of autoimmune disorders. MASP-2 is generated by the liver and is then released into circulation. Adult humans who are genetically deficient in one of the proteins that activate MASP-2 do not appear to be detrimentally affected by the deficiency. OMS721 is Omeros’ lead human MASP-2 antibody. Following discussions with both the FDA and the European Medicines Agency, a Phase 3 program for OMS721 in atypical hemolytic uremic syndrome (aHUS) is in progress. Also, two Phase 2 trials are ongoing. One is evaluating OMS721 in glomerulonephropathies, which has generated positive data in patients with immunoglobulin A (IgA) nephropathy and with lupus nephritis; the other has reported positive data both in patients with hematopoietic stem cell transplant-associated thrombotic microangiopathy (TMA) and in those with aHUS. In addition to potential intravenous administration, Omeros plans to commercialize OMS721 for one or more therapeutic indications as a subcutaneous injection and is also developing small-molecule inhibitors of MASP-2. Based on requests from treating physicians, Omeros has established a compassionate-use program for OMS721, which is active in both the U.S. and Europe. The FDA has granted OMS721 both orphan drug status for the prevention (inhibition) of complement-mediated TMAs and fast track designation for the treatment of patients with aHUS.
Omeros also has identified MASP-3 as the critical activator of the human complement system’s alternative pathway, which is linked to a wide range of immune-related disorders. In addition to its lectin pathway inhibitors, the company is advancing its development of antibodies and small-molecule inhibitors against MASP-3 to block activation of the alternative pathway.
About Omeros Corporation
Omeros is a biopharmaceutical company committed to discovering, developing and commercializing both small-molecule and protein therapeutics for large-market as well as orphan indications targeting inflammation, coagulopathies and disorders of the central nervous system. Part of its proprietary PharmacoSurgery® platform, the company’s first drug product, OMIDRIA® (phenylephrine and ketorolac injection) 1% / 0.3%, was broadly launched in the U.S. in April 2015. OMIDRIA is the first and only FDA-approved drug (1) for use during cataract surgery or intraocular lens (IOL) replacement to maintain pupil size by preventing intraoperative miosis (pupil constriction) and to reduce postoperative ocular pain and (2) that contains an NSAID for intraocular use. In the European Union, the European Commission has approved OMIDRIA for use in cataract surgery and lens replacement procedures to maintain mydriasis (pupil dilation), prevent miosis (pupil constriction), and to reduce postoperative eye pain. Omeros has clinical-stage development programs focused on: complement-associated thrombotic microangiopathies; complement-mediated glomerulonephropathies; Huntington’s disease and cognitive impairment; and addictive and compulsive disorders. In addition, Omeros has a proprietary G protein-coupled receptor (GPCR) platform, which is making available an unprecedented number of new GPCR drug targets and corresponding compounds to the pharmaceutical industry for drug development, and a platform used to generate antibodies.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, which are subject to the “safe harbor” created by those sections for such statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as “anticipate,” “believe,” “could,” “estimate,” “expect,” “goal,” “intend,” “look forward to,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “will,” “would” and similar expressions and variations thereof. Forward-looking statements are based on management’s beliefs and assumptions and on information available to management only as of the date of this press release. Omeros’ actual results could differ materially from those anticipated in these forward-looking statements for many reasons, including, without limitation, risks associated with product commercialization and commercial operations, unproven preclinical and clinical development activities, regulatory oversight, intellectual property claims, competitive developments, litigation, and the risks, uncertainties and other factors described under the heading “Risk Factors” in the company’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on May 10, 2017. Given these risks, uncertainties and other factors, you should not place undue reliance on these forward-looking statements, and the company assumes no obligation to update these forward-looking statements, even if new information becomes available in the future.
View source version on businesswire.com: http://www.businesswire.com/news/home/20170517005459/en/
Cook Williams Communications, Inc.
Jennifer Cook Williams
Investor and Media Relations
360-668-3701
Doc,
You as well, I will read article.
snup
Bret jensen just did an article on seeking alpha about omer
Always goes back up when he does
Got out of elite when volume dried up last week, hard to get out when it dips
But it dident
Hope elite does wel, but their board is full of pumping idiots
If approved i pump €200k into it the same day
Elite will go far when they launch sequestox. But for now, too much pumping based on hope
Good luck
Doc,
thankyou, nice trade on elite
ptie, I am going to wait for drop to below 3.50
but may not happen.
thanks again for your advise,
I have no position in omer, but I watch it.
snup
Sold before earnings due to the fact Q1 is always slow and rode elite from 17 to 22 back in omer now with only a 10% reduction, too much going on right now to be on the sidekine. gonna hold over a year and trade a few now and then, ptie is a bit too unsure for my comfort
Doc.
Did you make the trade with omer yet?
or are you a true believer in future?
Do you have an opinion on ptie?
1:7 rs and resubmission looks like early 2018
to me?
May fall to low 3's before dramatic move upwards
snup
OMER bullish 14.51
missed earnings and got a downgrade after the fact
flushed out people's stops and took their shares on a big hammer candlestick tail only to go back up
long term the chart continues to make a bullish base
bullish macd divergence
complex inverted head and shoulders pattern
normal chart
log chart
We must allow the short crowd time to cover for about 6 to 8 weeks. Short sqzz could power the 26+ level. Buy n hold play 2018.
Wish you were long on this one my friend, another amazing PR today
Opening is gonna be crazy
Doc,
Hearty congrats, I assume your still in omer?
I did not catch this ride but pleased for you.
snup
Finally, this moved up $1.50 in the last 20 minutes.
Keep it going boys, I need to make up for my NVAX losses from last year.
Golden cross and golden news
-- Additional Positive “Challenge-Rechallenge” Data Reported in Patient with Stem Cell Transplant-Associated TMA --
Omeros Corporation (NASDAQ: OMER) today announced presentation of a case report describing resolution of hematopoietic stem cell transplant-associated thrombotic microangiopathy (HSCT-TMA) in a dialysis- and transfusion-dependent adolescent girl who was treated with OMS721 under a compassionate-use protocol. The presentation “Resolution of acute kidney injury secondary to TA-TMA by the anti-MASP-2 monoclonal antibody OMS721 in a pediatric HSCT recipient” occurred at the 43rd Annual Meeting of the European Society for Blood and Marrow Transplantation in Marseille, France on Monday, March 27, 2017. Marco Zecca, M.D., Director of Pediatric Oncology at the Fondazione IRCCS Policlinico San Matteo, presented the data. OMS721 is Omeros’ lead human monoclonal antibody targeting mannan-binding lectin-associated serine protease-2 (MASP-2), the effector enzyme of the lectin pathway of the complement system.
The presentation describes a girl who developed HSCT-TMA following stem cell transplantation at 14 years of age. She was initially treated with eculizumab but did not tolerate treatment, developing pulmonary edema that recurred on retreatment with eculizumab. The HSCT-TMA became life-threatening and she required hemodialysis and daily platelet transfusions. Dr. Zecca, the patient’s physician, requested OMS721 for compassionate-use treatment and Omeros complied. Following OMS721 treatment, the patient was able to discontinue hemodialysis and to decrease substantially her platelet transfusion requirements. Recently, the patient’s dose of OMS721 was tapered, but she developed a viral infection that reactivated her HSCT-TMA. Her TMA was again successfully treated with restoration of the original OMS721 dose. To date, she has remained free of both dialysis and transfusions.
“This patient had severe TMA that I believe would have caused her death,” stated Dr. Zecca. “Her positive response to OMS721 treatment, both initially and following her virus-induced relapse during tapering, was impressive – the results of OMS721 treatment in this challenge-rechallenge scenario underscore the important effects of the drug. Since the poster was produced, her TMA has remained in remission and we have been able to discontinue her platelet transfusions. Her rapid response has been heartening, and we all are grateful for this remarkable outcome.”
Thrombotic microangiopathy is a potentially life-threatening complication of HSCT. Approximately 20,000 HSCT procedures are performed in the U.S. annually, and TMA is reported to occur in up to 30 percent of HSCT patients. Although the kidney is the most commonly affected organ, HSCT-TMA is a multi-system disorder and can also manifest clinically in the lungs, gastrointestinal tract and central nervous system. Reported mortality in patients with multi-organ involvement is greater than 90%. Even in patients who survive acute episodes, HSCT-TMA increases the risk for chronic kidney disease and end-stage renal disease.
About Omeros’ MASP Programs
Omeros controls the worldwide rights to MASP-2 and all therapeutics targeting MASP-2, a novel pro-inflammatory protein target involved in activation of the complement system, which is an important component of the immune system. The complement system plays a role in the inflammatory response and becomes activated as a result of tissue damage or microbial infection. MASP-2 is the effector enzyme of the lectin pathway, one of the principal complement activation pathways. Importantly, inhibition of MASP-2 does not appear to interfere with the antibody-dependent classical complement activation pathway, which is a critical component of the acquired immune response to infection, and its abnormal function is associated with a wide range of autoimmune disorders. MASP-2 is generated by the liver and is then released into circulation. Adult humans who are genetically deficient in one of the proteins that activate MASP-2 do not appear to be detrimentally affected by the deficiency. OMS721 is Omeros’ lead human MASP-2 antibody. Following discussions with both the FDA and the European Medicines Agency, a Phase 3 program for OMS721 in atypical hemolytic uremic syndrome (aHUS) is in progress. Also, two Phase 2 trials are ongoing. One is evaluating OMS721 in glomerulonephropathies, which has generated positive data in patients with immunoglobulin A (IgA) nephropathy; the other has reported positive data both in patients with hematopoietic stem cell transplant-associated thrombotic microangiopathy (TMA) and in those with aHUS. In addition to potential intravenous administration, Omeros plans to commercialize OMS721 for one or more therapeutic indications as a subcutaneous injection and is also developing small-molecule inhibitors of MASP-2. Based on requests from treating physicians, Omeros has established a compassionate-use program for OMS721, which is active in both the U.S. and Europe. The FDA has granted OMS721 both orphan drug status for the prevention (inhibition) of complement-mediated TMAs and fast track designation for the treatment of patients with aHUS.
Omeros also has identified MASP-3 as the critical activator of the human complement system’s alternative pathway, which is linked to a wide range of immune-related disorders. In addition to its lectin pathway inhibitors, the company is advancing its development of antibodies and small-molecule inhibitors against MASP-3 to block activation of the alternative pathway.
About Omeros Corporation
Omeros is a biopharmaceutical company committed to discovering, developing and commercializing both small-molecule and protein therapeutics for large-market as well as orphan indications targeting inflammation, coagulopathies and disorders of the central nervous system. Part of its proprietary PharmacoSurgery® platform, the company’s first drug product, OMIDRIA® (phenylephrine and ketorolac injection) 1% / 0.3%, was broadly launched in the U.S. in April 2015. OMIDRIA is the first and only FDA-approved drug (1) for use during cataract surgery or intraocular lens (IOL) replacement to maintain pupil size by preventing intraoperative miosis (pupil constriction) and to reduce postoperative ocular pain and (2) that contains an NSAID for intraocular use. In the European Union, the European Commission has approved OMIDRIA for use in cataract surgery and lens replacement procedures to maintain mydriasis (pupil dilation), prevent miosis (pupil constriction), and to reduce postoperative eye pain. Omeros has clinical-stage development programs focused on: complement-associated thrombotic microangiopathies; complement-mediated glomerulonephropathies; Huntington’s disease and cognitive impairment; and addictive and compulsive disorders. In addition, Omeros has a proprietary G protein-coupled receptor (GPCR) platform, which is making available an unprecedented number of new GPCR drug targets and corresponding compounds to the pharmaceutical industry for drug development, and a platform used to generate antibodies.
Impressive pipeline CC and financials but price isn't moving, weard.
Manipulation?
Doc,
Thanks, just starting to read it.
snup
ALXN's Soliris ($3B annual sales) is administered by a 2 hour Intravenous Transfusion at a medical facility vs. Omeros'(500mil market cap) OMS721 administered by a shot at home
Q4 EPS of -$0.45 beats by $0.11.
Revenue of $12.9M (+93.7% Y/Y) beats by $0.42M.
very bullish CC
Omeros Corporation (NASDAQ:OMER)
Q4 2016 Earnings Conference Call
March 16, 2017, 16:30 ET
Executives
Mark Metcalf - IR
Greg Demopulos - Chairman & CEO
Mike Jacobsen - Chief Accounting Officer
Analysts
Tyler Van Buren - Cowen & Company
Thomas Yip - FBR and Company
Liana Moussatos - Wedbush Securities
Steve Brozak - WBB Securities
Serge Balenger - Needham & Company
Elemer Piros - Cantor Fitzgerald
Jason Kolbert - Maxim Group
Operator
Welcome to today's conference call for Omeros Corporation. At this time, all participants are in listen-only mode. After the company's remarks, we will conduct a question-and-answer session. Please be advised that this call is being recorded at the company's request and a replay will be available on the company's website for one week from today.
I'll turn over the call to Mark Metcalf from Omeros. Sir, you may begin.
Mark Metcalf
Good afternoon and thank you for joining the call today. I'd like to remind you that some of the statements that will be made on the call today will be forward-looking. These statements are based on management's beliefs and expectations as of today only and are subject to change. All forward-looking statements involve risks and uncertainties that could cause the company's actual results to differ materially. Please refer to the Risk Factor section of the company's annual report on Form 10-K which was filed today with the SEC for a discussion of these risks and uncertainties.
Dr. Greg Demopulos, Chairman and CEO of Omeros will take you through a corporate update and then Mike Jacobsen, our Chief Accounting Officer will provide an overview of our fourth quarter and year-end financial results. We have some time reserved for questions after the financial overview.
Now, I would like to turn the call over to Dr. Greg Demopulos.
Greg Demopulos
Thank you Mark and good afternoon everyone. We appreciate all of you joining us today. 2017 is shaping up to become a breakout year for Omeros. In 2016 we laid the foundation that will make that possible. Much of that groundwork was solidified in the achievements and successes of the fourth quarter of 2016. Since the broad market launch of a Omidria our commercial product for use during cataract and lens replacement surgery and net revenues have consistently delivered double digit quarter over quarter growth and the fourth quarter of 2016 was no exception. Net revenues of Omidria for the quarter were $12.9 million. This represents a 14% increase over the third quarter of 2016 and on a year over year basis a 212% increase over 2015.
This revenue growth was the result of broad based successes including one, an increase in the number of what we call standard of use accounts or those using Omidria in more than 50% of their procedures Two, an increase in the number of new accounts ordering Omidria, three, an increase in the total number of unique accounts purchasing Omidria during the quarter and four, an increase in the number of daily orders.
Total vials sold in the fourth quarter increased at an even greater rate, 22% over the third quarter and 223% year over year. The difference between the gross and net revenue and the greater growth in vials sold as a reflection of increased gross to net the deductions in the fourth quarter. This increase in gross to net was anticipated and primarily driven by the increased utilization of the Omidria share reimbursement assistance services and our volume discount purchase program which we introduced in November.
The volume discount program provides ambulatory surgery centers or ASCs with rebates based on certain minimum purchase levels of a Omidria. Although this program has been in the market for a relatively short time we have seen early success among the growing number of participants with broader utilization in existing accounts as well and as a meaningful increase in new accounts enabling us to provide the benefits of Omidria to even more patients.
Earlier last year we also initiated an inventory on consignment program for a Omidria. This together with our volume discount program has helped to accelerate growth of Omidria sales. Going forward we expect that facilities will increasingly make use of both volume discounts and consignment. While these programs expand our gross to net deductions, the deduction should be more than offset by the increased growth in Omidria sales. As has been one of our objectives, sales of Omidria at hospitals have continued to grow and mirror the split nationally for cataract surgery. Roughly 35% in hospital outpatient departments and 65% in ambulatory surgery centers. We have focused on increasing our penetration in the hospitals because while perhaps slower to adopt new products once they do adopt they tend to remain long term customers. Teaching hospitals or academic centers are particularly important given their ability to influence physician practices locally and regionally.
This effect on regional practice patterns as enhanced through the residency programs at these teaching institutions. Graduating residents also often incorporate the methods, procedures and products that they used during their training. This is especially true of surgical residents including a foul mix surgery residence [ph]. Omidria is currently in use at approximately 20 large academic centers including New York Eye and Ear, the highest volume cataract surgery hospital in the country. Other major academic centers using Omidria include Massachusetts Eye and Ear, Duke University, Wake Forest University, Yale University, Weill Cornell Medical Center, University of California, San Francisco, Indiana University [indiscernible] Medical Center, University of Kentucky, Moran Eye Center at the University of Utah, University of Virginia and University of Minnesota. Support for Omidria also continues to grow among a [indiscernible] surgeons. As an increasing number of cataract thought leaders and physicians accumulate experience with Omidria podium and panel discussions of the product are regular features at cataract surgery conferences. Omidria received positive and prominent exposure at ophthalmology meetings throughout 2016 and this exposure has accelerated into 2017. In November we announced the successful completion of the post marketing Omidria paediatric clinical trial. In the trial Omidria was well tolerated with adverse event rates consistent with those seen in paediatric cataract surgery and in the control group.
We plan to submit a supplemental NDA this year requesting expanded label language to cover patients of any age. We also expect that this submission will result in an additional six months of regulatory exclusivity for Omidria. International sales of Omidria also began in the fourth quarter. Under our agreement with ITROM distribution of Omidria was initiated in the Kingdom of Saudi Arabia. Local regulatory applications are pending approval in the region including in the United Arab Emirates. Approvals are expected throughout this year which should lead to expanded sales across the Middle East. In addition to our partnership in the Middle East we are currently exploring similar arrangements for the sale of Omidria in other international regions. So we continue to grow Omidria revenues in the U.S. and now internationally as well.
We have seen the resistance to adoption of Omidria fade particularly with respect to any lingering questions about clinical efficacy. The data are clear, there is no product that provides the clinical benefits of a Omidria. Reimbursement concerns are also dissipating as payer coverage continues to increase and more and more facilities access our Omidria share reimbursement services. Our volume purchase discount program is driving additional sales in existing accounts and enabling new accounts to begin building and growing their experience with Omidria.
We are seeing growth across both hospitals and ambulatory surgery centers that mirrors the national %age splits for cataract surgery in these two settings.
Omidria became cash flow positive as a program within three quarters of its launch. Our objective now is for Omidria to generate sufficient revenues to fund our pipeline as well and we expect to achieve that. We also are working hard to secure a separate payment for Omidria following expiration of pass through on January 1, 2018. Our efforts on this front are focused on both legislative and administrative solutions and while we alone do not control the outcome we expect that we will be successful because providing Medicare beneficiaries with broad access to innovative drugs used during surgical procedures is the right thing to do. Stated conversely denying Medicare beneficiaries access to innovative drugs is an untenable position.
Let's turn now to our pipeline, because of their importance I'm going to focus on the following assets. Our complement programs, our PDE and addiction programs and our GPCR's. I'll begin with our complement program focused on Mannan-binding lectin-associated serine protease-2 or MASP-2. MASP-2 is the effector enzyme of the lectin pathway of the complement system, a key component of the immune response. OMS721 is our highly potent and selective antibody against MASP-2 and currently is being evaluated in three clinical programs, typical Hemolytic Uremic Syndrome or aHUS, IgA nephropathy and hematopoietic stem cell transplant-associated TMA, thrombotic microangiopathy or stem cell transplant associated TMA. Enrolment opened this year for our OMS721 Phase 3 program in aHUS. As previously reported from our Phase 2 trial we have seen improvements across TMA markers in aHUS patients treated with OMS721 and to-date a good number of patients have been able to discontinue dialysis. Fastrack status for aHUS was granted by FDA. The Phase 3 trial design was discussed with both FDA and DMA and will consist of one study that will be single arm and open label in other words no control arm and we expect that this one study will satisfy both regulatory agencies. The design will be similar to that conducted for Solaris in the same indication. Based on our discussions with both FDA and DMA 40 patients could provide full approval in Europe and approximately the same number of patients would be required for accelerated approval in the U.S. FDA suggested that we consider and we plan to pursue accelerated approval. To-date we have also received orphan drug designation from the FDA for TMA's broadly including aHUS. Additional data on our aHUS program will be presented at the World Congress of Nephrology in late April. We also have an ongoing Phase 2 program in patients with IgA nephropathy and other glomerulopathies. In October we released statistically significant positive data on IgA patients treated with OMS721. OMS721 significantly improved key end points of renal function and patients achieved partial remission with just 12 weeks of dosing. We continue to follow these patients and after dosing was stopped renal function continued to improve and to our knowledge none of these patients have relapsed. Subsequent data in additional IgA nephropathy patients have demonstrated similar benefits.
Given our data and that there is no current treatment for IgA nephropathy we will submit a full application for breakthrough designation and have discussed with FDA both accelerated approval and a significantly shortened timeline to full approval. We also are preparing a submission for EMA's priority medicines or prime designed to accelerate evaluation of drugs that based on early clinical data offer a major therapeutic advantage over existing treatments or benefit patients for whom there is no treatment option at all. Our Phase 3 program and IgA nephropathy is slated to begin later this year. We continue to evaluate data from our Phase 2 glomerulopathy trials and plan to share more study results in the near future.
Our other OMS721 Phase 2 program is evaluating the drug in patients with stem cell transplant associated TMA. Here again last quarter we announced statistically significant positive Phase 2 clinical data OMS721 in these patients. To-date we have treated nine patients with life threatening post-transplant TMA's and seven of those patients improved. The other two patients received only two to three weeks of OMS721 treatment due to reasons unrelated to the drug. They were managed palliative and died. In contrast patients who completed protocol specified treatment with OMS721 showed meaningful improvement in platelet counts and measures of red blood cell destruction specifically lactate dehydrogenase and haptoglobin levels. These data were presented in February at the tandem meeting of the American Society of Blood and Marrow transplantation and the Center for International Blood and Marrow Transplant Research.
OMS721 has received FDA's orphan drug designation for TMA's. As with IgA nephropathy there is no approved treatment for stem cell transplant associated TMA and here again we plan to pursue breakthrough designation and accelerated approval from FDA as well as the EMA's prime designation. Our Phase 3 program stem cell associated TMA like our Phase 3 program for IgA nephropathy is planned to initiate later this year. Our OMS721 compassionate use program continues to provide treatment to patients internationally. These are patients who for whatever reason are not eligible for our clinical trials and do not and who do not have or have exhausted other treatment options. This program has provided OMS721 treatment to patients with a aHUS, stem cell transplant associated TMA and glomerulopathy including patients who have failed or not tolerated treatment with Solaris.
To provide some perspective here is an example of a compassionate use patient, a 15 year old girl with Diamond-Blackfan anemia which is a congenital disorder that almost exclusively affects red blood cells. The patient underwent stem cell transplantation and subsequently developed TMA. She was treated with Solaris, responded but developed pulmonary edema and Solaris treatment was stopped.
Her TMA relapsed and she again was treated with Solaris, this time at a low dose and again developed pulmonary edema. She was requiring platelet transfusions every day together with haemodialysis almost every other day to keep her alive. Her physician requested that we provide OMS721 under compassionate use and of course we did. Within three weeks of beginning OMS721 she came off dialysis. Her platelets recovered and her transfusions were tapered and then discontinued. By Christmas she was at home with her family and she continues to do well.
The girl's recovery while more dramatic because of her young age is consistent with the improvements in TMA markers that we have observed in stem cell TMA patients who have been treated with OMS721 in the clinical trial. The mortality rate for severe TMA is 90% or higher and again we have observed TMA improvement in all patients who completed treatment with OMS721.
Now I'd like to discuss the other half of our complement franchise, our MASP-3 inhibitor OMS906. The Omeros team was the first to identify MASP-3 as the primary activator of the alternative pathway. So from a patent perspective we control the key activators of two of the three pathways in the complement system namely the lectin pathway and the alternative pathway and we now are also developing molecules that inhibit the key activators of the third or the classical pathway. We have reported positive data and well except in animal models of arthritis and paroxysmal nocturnal hemoglobinuria, or PNH. Given the substantial advantages demonstrated over a C-5 inhibitor in these PNH studies we are preliminarily slating PNH as the first clinical indication for OMS906. Currently we are finalizing selection of our lead and backup molecules and are preparing to initiate scale up for clinical trials.
With respect to how we plan to deliver our MASP-2 and MASP-3 inhibitors for OMS721 we have both intravenous and subcutaneous formulations and we plan to commercialize both for different indications. For OMS906 we plan to develop a subcutaneous formulation to add to our IV formulation. In both our OMS721 and OMS906 programs we also are aggressively developing small molecule inhibitors against MASP-2 and MASP-3 respectively.
Let's now turn to our phosphodiesterase 7 or PDE7 inhibitor program for addiction and compulsive disorders. PDE7 is considered one of the most exciting targets for addiction and Omeros through our issued patent position controls the use of any PDE7 inhibitor for the treatment of any form of addiction or any compulsive disorder. With consistently positive pre-clinical results in cocaine, alcohol, nicotine and opioids as well as in binge eating the data show that our PDE7 inhibitors decrease craving as well as both cue and stress induced relapse. Importantly studies demonstrate that PDE7 inhibitors accomplish these effects without depressing the reward system, a problem that seriously hinders the use of currently approved and the addiction agents. We believe that we have elucidated the mechanism for PDE7 inhibitors and addiction and we are finalizing a manuscript for submission to a leading peer reviewed scientific journal outlining this mechanism.
IND enabling studies are underway as this is the selection of the initial indication and we are currently targeting the submission of an IND or CTA in late 2017 for clinical trials to begin in early 2018. The other half of our addiction franchise is OMS405 our PPAR-gamma agonist program. Omeros has broad issued and pending patents covering the use of any PPAR-gamma agonist in the treatment of any form of addiction or compulsive disorder. During the fourth quarter, we announced positive results from a Phase 2 clinical trial evaluating the effects of a PPAR-gamma agonist in patients with cocaine use disorder. This trial demonstrates that the PPAR-gamma agonist reduces craving and improves the integrity of brain white matter in patients with cocaine use disorder.
We also announced positive data from a Phase 2 clinical trial of evaluating the effects of a PPAR-gamma agonist in heroin dependent subjects. The clinical drug trial administered a PPAR-gamma agonist for up to three weeks in heroin users who are maintained on sub-lingual combination of buprenorphine and naloxone. The findings demonstrated a statistically significant reduction both in drug craving and in measures of anxiety.
With respect to our phosphodiesterase 10 or PDE10 inhibitor program we're evaluating the data from Pfizer's clinical trial in Huntington's disease and Takeda's clinical trial in schizophrenia using their respective PDE10 inhibitors. Each of those trials failed to meet its end point. In retrospect, our decision to await these data before launching into one or more large clinical trials in these indications appears to have been a wise one. Despite the recent misses by Pfizer and Takeda we believe that there is a role for PDE10 inhibition in CNS disorders. We are evaluating other potential indications and assessing our options to move forward. Given our successes in the other programs that we have discussed today we currently have prioritized those programs over PDE10.
Let's wrap up the overview of our development progress with a brief update on our GPCR program. We believe that Omeros exclusively controls [indiscernible] or functionally active compounds for 54 of the 81 Class A orphan GPCRs. We are advancing pre-clinical programs on a number of these exciting targets for which Omeros alone has compounds. The indications include triple negative breast cancer, demyelinating diseases such as multiple sclerosis, appetite and eating disorders and osteoporosis and seasonal effective disorder. In the fourth quarter, we also release data around another receptor that we control GPR174. GPR174 appears to play a unique role in the immune system and we believe that Omeros is the only entity with compounds that block GPR174. We have shown that our compounds in human lymphocytes and monocytes boost the immune response by elevating levels of specific cytokines also resulting in reduction of regulatory t-cells or t-regs. Inhibiting GPR174 represents a novel approach to immune therapies for cancer and potentially for treating other immunologic disorders. Compound optimization and animal studies are ongoing and we expect that you will hear more about this program over the coming months.
With that I will turn the call over to Mike who will lead us through our fourth quarter financial results.
Mike Jacobsen
Thanks, Greg. As Greg noted revenue for the fourth quarter was $12.9 million, all of which was from Omidria products sales. This is an increase of $1.6 million over the third quarter. Our net loss for the fourth quarter was $19.6 million or $0.45 per share, this includes a loss on early extinguishment of debt of $5.6 million or $0.13 per share related to the prepayment of our previous loan agreement. During the fourth quarter, noncash expenses were $5.2 million or $0.12 per share.
Now I will address some details regarding the third versus the fourth quarter. Our reported revenue for the quarter increased 14% from the third quarter while vials of a Omidria sold to our distributors increased by 22% over the third quarter. The difference between these two values is primarily the result of increased gross net deductions in the fourth quarter as the overall price that we receive per unit sold was reduced as we had expected due primarily to the November introduction of our volume purchase discount program. This program has had a net positive impact on our unit sales because we gained new customers and saw the volume of purchases increase in existing accounts that participated in the program. In addition for those existing accounts our incremental revenues were greater than the rebates earned.
Costs and operating expenses for the fourth quarter were $24.8 million, an increase of $1.4 million from the third quarter. The increase was primarily related to noncash employee stock options grants made during the fourth quarter for 2015 performance. As I mentioned earlier during the fourth quarter we incurred a $5.6 million loss on early extinguishment debt related to the prepayment of our previous loan agreement.
Turning to the balance sheet in October 2016 we entered into a six year $125 million secured debt facility with CRG. The facility is interest only through December 31, of 2020 and incurs interest at 12.25%, 4% of which we can defer and add to the outstanding principal at our option through March of 2021. This facility is secured by substantially all of our assets. We borrowed the first tranche of $80 million at closing and used most of the proceeds to retire previously existing debt. We also have the ability to borrow an additional $25 million through September 19th of 2017 if we achieved at least $18 million of Omidria product revenue during any consecutive three month period prior to June 30, 2017 or achieve an average market cap of $700 million during any consecutive three months prior to the June 30, 2017.
We can also borrow an additional $20 million through March 21 of 2018 assuming we achieved Omidria product revenue of at least $25 million during any consecutive three month period or an average market cap of $1 billion during any consecutive three month period prior to December 31, 2017. The new CRT facility has substantially lower annual revenue covenants and our previous loan agreement while also providing an alternative means to satisfy the covenants by achieving market cap thresholds. The revenue requirement for 2017 which is defined as total GAAP revenue is $55 million and the market cap at our current borrowing levels is about or approximately $525 million. In addition any revenue short fall that we could possibly incur can be addressed by paying the amount of the shortfall towards the outstanding principal from qualified borrowings or sales of our common stock.
As of December 31, 2016 we had $45.3 million of cash, cash equivalents and short term investments available for general operations. In addition, we had $5 million of restricted cash as required by our loan agreement and then addition $835,000 of restricted cash and investments available to support our building leases and other operating leases.
Now let's take a look ahead, with regards to revenue we expect that our Omidria revenues will continue to grow throughout 2017. With respect to R&D we have stated in prior calls that we will adjust our research and development spending up or down based on a variety of factors including Omidria product revenues, licensing opportunities, clinical results and overall business conditions. We anticipate that during 2017 the majority of our research and development expenses will be related to Phase 3 and Phase 2 clinical programs or OMS721 and the preparation for commercial manufacturing of 721. Selling, general and administrative expenses for 2017 are expected to increase slightly from the fourth quarter of 2016's run rate. This is primarily due to the costs associated with sales and marketing programs and increased legal costs and pursue the patent infringement claims against Par Pharmaceuticals effort to receive FDA approval for a generic version of Omidria. Interest expense associated with the $80 million outstanding under our credit facility will be approximately $3 million per quarter of which approximately $800,000 can be deferred at our option.
With that I would like to turn the call back over to Greg for Q&A.
Greg Demopulos
Thanks Mike. Let's open the call to questions.
Question-and-Answer Session
Operator
[Operator Instructions]. Our first question comes from Tyler Van Buren from Cowen & Company. Your line is now open.
Tyler Van Buren
Congratulations on the disclosure of beginning the enrolment of the Phase 2 trial and aHUS for 721, clearly a very positive update. So just you know and for what is a disease a very severe patients have to imagine that the agency has a lot of confidence in the efficacy of 721 to allow you guys to go ahead and go into a Phase 3 trial so curious maybe to just hear a little bit more about your end of Phase 2 meeting discussions with the FDA and how that went?
Greg Demopulos
We don't discuss specifics about those meetings Tyler and first thank you for your comments, appreciate it. What we have disclosed from that meeting was our discussion around the design and specifically that the design for the Phase 3 trial will be a single study, single arms so open label, no control arm and the design will be very similar to that which was required for Solaris approval for their BLA. So we again remain confident as you pointed out in our drug and we look forward to completing that clinical trial. Really the interesting part of this is as we've been moving forward with aHUS we have had two other programs sort of rapidly accelerating through development and those as you are the IgA nephropathy study as well as the other nephropathies meaning membranous, lupus nephritis and also our stem cell transplant related TMA studies. So we really have a full plate here with OMS721. To-date we have not found a maximally tolerated dose with 721, we're feeling very good about the safety profile of the drug and clearly we're feeling good about the efficacy that we see at least the apparent efficacy that we see with the drug.
Tyler Van Buren
Okay. Can you tell us what the plan dosing regimen is for Phase 3 and also in terms of timelines when we might see the top-line data from the study?
Greg Demopulos
Phase 3 will be, we expect primarily subcutaneous administration. With respect to the timelines on data we've not made those public yet. We'll keep you informed Tyler as we have more information about timelines and additional data from that study.
Tyler Van Buren
Okay, great. And just one final one 721, as you think about the broader Phase 2 patient population and the efficacy data and try to compare that to what we've seen historically with Solaris. What do you think are the most relevant end points to compare and perhaps can you give us any insight into maybe the percent of patients with the complete TMA response or event free status? Curious to maybe hear a little bit more about that and maybe also potential timing on a publication or plans to submit one?
Greg Demopulos
We haven't released the data that you're requesting there from the Phase 2 program I mean certainly we think that our drug will compare well to Solaris, we also are pleased with the potential safety differences between them. As I mentioned in our initial comments that we will have additional data from the aHUS study in late April at the International Meeting that I mentioned.
Tyler Van Buren
Okay, great. And on Omidria with respect to the C-code transition that you referred to at the end of the year and going into 2018 maybe just a little more granularity on the mechanics there and how should we expect the price to potentially change for the product, any insight there would be helpful.
Greg Demopulos
Yes I think with respect to granularity of our efforts you know we don't want to get too specific about what we're doing other than that we are pursuing a dual pronged approach, one is legislatively and the second is administratively. So we're obviously working through congressional avenues, the second working with CMS directly. I think that there is a good amount of support for the concept that drugs use during surgical procedure should not be packaged. So stated conversely again that drugs used during surgical procedures should be separately paid, really just like almost all other drugs. And we expect again that we will be successful in this effort. With respect to pricing following January 1, 2018 I think that it's a bit premature to discuss that. We're doing well with the product now, let's see how we've progress throughout the year and I think that's a discussion that we can have once hopefully we are successful in securing a long term reimbursement for Omidria.
Operator
Our next question comes from Thomas Yip from FBR and Company. Your line is now open.
Thomas Yip
Very happy to see progress in Omidria and also 721 there earlier, [indiscernible] as well. So first a question regarding the Phase 3 trial of 721 and aHUS. So the finalization of the trial designs and specifically in clinicatrials.gov is that contingent on the FDAs decision on the accelerated approval application that you will file?
Greg Demopulos
No, as you know there is no specific accelerated approval application. Accelerated approval is a process and that is pursued through ongoing discussions with FDA and is based upon in good part data that we present to the FDA from the Phase 3 program.
Thomas Yip
Right. So what factors do you think the FDA will look at most importantly in making that decision in a Phase 3 data? Are there other factors that could persuade them to approve accelerated approval?
Greg Demopulos
I think it will depend on the data that we generate, it will depend on classes of patients, groups of patients that we can treat that perhaps Solaris cannot, it may also tie into potential safety differences between the two drugs remember that 721 does not inhibit the [indiscernible] of the classical pathway which is required for antigen anti-body complexing that is your -- remember the classical pathway is your acquired immune response. So I think there are multiple areas, Thomas, I hope that answered your question.
Thomas Yip
Yes I guess the most important thing to see is some preliminary data from Phase 3 and also we expect to hear more about the ongoing Phase 3 trial as well. So I'm going to switch gears and talk about Omidria a little bit, at which revenue level do you expect to begin providing revenue guidance for Omidria?
Greg Demopulos
I'm not sure, it's a good question. We have made the decision at present that we're not going to add and we have not guided. I think at some point as the market stabilizes, as we are able to appropriately and relatively accurately project those revenues we will consider it I think that now though that that is premature.
Operator
Our next question comes from Liana Moussatos from Wedbush Securities. Your line is now open.
Liana Moussatos
For OMS721 you're going to have data presentations in April at the World Congress and in June at Renal Diseases, how are those data sets different from what we've already seen that you probably disclosed, will there be more patients, will all the patient data be presented -- what's going to be different at those two meetings?
There will be data at those meetings and in those presentations that will be from ongoing clinical work.
Liana Moussatos
Okay. So there will be interim preliminary data that we haven’t seen yet or full data from?
Greg Demopulos
Yes.
Operator
Our next question comes from Steve Brozak from WBB Securities. Your line is now open.
Steve Brozak
Let me dive into a couple of quick questions, since lots has asked and answered. On the OMS721 you're going to be conceivably running multiple trials 721 where you could in theory see data that actually comes back that is better in some areas than in others, can you give us any feedback in terms of what you're seeing as far as what the clinicians are giving you on that kind of guidance because obviously you know one of the things that is really important are the specific clinicians that are treating the patients, what do they expect and what's what your feedback on that so far?
Greg Demopulos
Well obviously from the incidence of compassionate use request, I would think that they are seeing the data as positive and helpful to their patients. I think you've raised a good point. We have multiple trials running at one time, Steve and really the question is how do we get OMS721 across the finish line meaning how do we get it commercialized as quickly as possible and that's really our focus here and I think the beauty of what we are seeing now is that we really do have multiple shots on goal within 721.
Steve Brozak
About those multiple goals with IgA and stem cell, can you go into more detail about that because that's something that I think you mentioned but it is critically important.
Greg Demopulos
Yes I can to whatever extent I am allowed to do here but I will tell you that look we're very pleased. Let me take a step back, we're in a Phase 3 program on aHUS, we've met with FDA and EMA, we're feeling comfortable with what we need to do to get that indication approved for OMS721. So let's put right now aHUS aside and talk about what I think you're asking which is the IgA and stem cell transplant programs for 721. I will tell you that we are very excited about the data that we are seeing in both of those indications. I believe that also you had mentioned how are the physicians viewing those data. I think it is fair to say that those physicians who treat these patients are equally excited about the potential for OMS721 in these indications. We have had dialogue with FDA around these programs. We will continue to do so. We will put out additionally more data from these programs. I think and I think I see where you're going with this, I want to make sure I'm answering your question Steve but these programs each of them or both of them could accelerate quite quickly and we are really looking at all three of these programs and we're controlling the dials across all three and again the objective is to get OMS721 into the market as quickly as possible with really any of the three indications and that will continue to build upon itself, that's the objective, that's our focus from what we're seeing today with all of the appropriate caveat we do expect that we will be successful.
Steve Brozak
Right, I will quickly switch and last question. On Omidria, you obviously you iterated all the significant teaching centers that you're in right now. Given the fact that you transition from teaching centers obviously to other hospital forms regionals and as such, can you give us some feedback even if it's anecdotal on what you've seen on how the teaching centers have started to adopt Omidria and what you would expect to happen as far as how it will start to translate and obviously penetrate the healthcare system.
Greg Demopulos
Sure. Let's just take an example of one of those institutions I mentioned New York Eye and Ear, New York Eye and Ear performs more cataract surgery procedures annually than any other hospital in the United States. These types of institutions are usually slower to adopt just because of their size, just because of the layers of bureaucracy, but their physicians and frankly the pharmacist as well when looking at all of our data pushed hard for the ability to bring Omidria into the facility. Utilization within that facility has continued to expand, the number of physicians using it within the facility has continued to increase and the procedures have increased and then you get the satellite effect from other institutions located other facilities located around New York Eye and Ear that look to New York Eye and Ear to see what is New York Eye and Ear doing in-patient care and when they see that Omidria is an important component of that patient care you know that has an effect and I think that we're seeing that not just in New York Eye and Ear but really at all of those institutions that I mentioned. Duke, Wake Forest, Mass Eye and Ear, UCSF, all of those that I mentioned have that satellite effect or that ripple effect that that really does translate to increased utilization regionally not just locally but I think regionally and the importance of that is also the residency programs right, I mean these are young surgeons in training who are likely going to have more difficulty performing surgery than those who are well versed with years of experience in cataract surgery. Certainly these are young doctors who can benefit from Omidria. And also once they use that product in their training program they tend and very frequently tend to adopt those same routines, those same products, those same practices when they move into private practice or when they move into an academic position at some other institution. So it's an effect seeding future use of Omidria and I think we've seen that pretty clearly.
Operator
Our next question comes from Serge Balenger from Needham & Company. Your line is now open.
Serge Balenger
A couple questions first on Omidria, Greg in lieu of the 2017 guidance can you talk maybe about -- if you're seeing some of the same seasonality we saw last year in the early part of '17 and where do you expect growth to come from in Omidria and -- do you expect any impact on pricing given that we should see additional use of the volume discount program.
Greg Demopulos
In response to your first question, yes we see some of the seasonality not to the same extent that we have previously but certainly. I don't think it's any secret that cataract surgery and other surgical procedures are slower in the early part of the year simply because of how insurance rolls over and those deductible period start anew at the beginning of the year which tends to have patients putting off surgery until a good part of that deductible is already eaten through and they don't have to absorb all of that cost in the early part of January but as I said we're seeing not -- the extent of that is less than what we had previously seen.
With respect to where we think the growth is coming from and will come from in the future I think it's going to come from hospitals and ASC's I think it's coming from expanding utilization within our existing accounts and from a wholly new accounts who are starting to use Omidria. Certainly I think that the very early resistance that we had around Omidria that certainly seems to have waned substantially particularly as I mentioned earlier just the clinical pushback that, gee is this really a product necessary? Does it really do what we need it to do? I think that it is very difficult for someone to take an opposing position to the fact that Omidria does do all of that. I think it's very difficult to take that opposing position credibly when you look at the data. The third question that you asked is what about pricing with respect to the discount program. We still have been able to almost wholly maintain our ASP even with these discount programs. We continue to expect to do these programs in a very smart way and we're monitoring it closely you know remember that our price initially was set as a requirement to qualify for pass through, there's a threshold above which the price needs to be to qualify for pass through. But at some point here we're not going to be limited to that threshold but we're still comfortable with how our pricing is progressing .
Serge Balenger
Back to the -- you're to make further entry into the hospital segment, can you talk about the evaluation process that these P&T committees go through usually pretty focused on costs just how they look at Omidria?
Greg Demopulos
Certainly we've been successful. I mean our distribution across hospitals and ASCs now as we've said reflects exactly what the distribution across the U.S. is. Approximately 35% in hospitals, 65% in ASCs, so we've clearly been successful there. You are correct that they do focus on cost. They also do though focus on clinical benefit and I think that we clearly make a very strong case with respect to clinical benefit. Remember too that a number of these hospitals, these large institutions are 340B facilities. So these are facilities that qualifies 340Bs by treating a sufficient percentage or number of indigent patients and by virtue of their being 340B or having 340B status they are then afforded government mandated discounts. So the 340B program also helps in sort of the entrée search to these hospitals and those initial discussions with the P&T committees and then I think it's really the clinical data that ends up carrying the day and closing that arrangement.
Serge Balenger
Okay. And then just regarding potential European partnerships on Omidria, is that still the plan to enter partnership into '17, if I remember correctly that EU marketing authorization have a shelf-life and how will that affect your partnership discussion?
Greg Demopulos
Once again you're spot on and yes we do plan to partner in 2017, but that’s all I will say about that at this point.
Operator
Our next question comes from Elemer Piros from Cantor. Your line is now open.
Elemer Piros
What I would like to ask is when I look at the historical numbers, quarter and quarter there is a very steady, predictable linear growth in Omidria sales. So my question is that do you see at some point in 2017 perhaps and what would precipitate a divergence from this trend and we're hoping for an upgrade for this to become more of an exponential sort of growth.
Greg Demopulos
Yes I understand, yes we would much prefer that to be a kink up than a kink down. And answer to your question about the kink in that curve yes that's clearly one of our major objectives is to put an upward kink in that curve. We do believe that we can do that. We believe that the programs were initiating help to do that. We also believe that at some point there's a threshold of critical mass with respect to users and once we exceed that we also think that that will help bend that curve upward more steeply than that linear growth that you referenced. Surgeons in general and it appears that a mix surgeons perhaps even more so than many others are conservative but they're slow to adopt new products but once they reach that initial threshold then that growth really picks up. I'll use as an example Viscoelastics, if you look at the adoption rate of this Viscoelastics in their early years of availability to a [indiscernible] surgeon, the percentage penetration was really minimal, low single digits and yet now when you look at Viscoelastic devices what you see is that they are mainstay. They're used in effectively in all procedures and I think that this is somewhat reflective of surgery in general but certainly I think of [indiscernible] surgery in particular.
Elemer Piros
And in the 721 trial would you please confirm that in previous patients, previously treated aHUS patients you also used subcutaneous dosing.
Greg Demopulos
I will neither confirm nor deny that at this point.
Elemer Piros
But in the Phase 3 we're doing that subcu?
Greg Demopulos
Yes.
Elemer Piros
And often would they be dosed?
Greg Demopulos
We've not discussed dosing regimen publicly.
Elemer Piros
Okay. And one last question on the nephrology conference that you highlighted, if you could tell us just qualitative maybe somewhat quantitatively how many patients worth of data would we see, would we see a follow up data from the very earliest patients that you treated?
Greg Demopulos
I will answer that question in this way Elemer, we have to-date put out only two patients from the IgA study. I am confident in telling you that at the conference presentation you will see more patients than what we have already put out publicly and you will see additional data on those patients for whom we have already released data. So you will see more data on the existing patients for those who are already out in the public domain and you will see -- I expect new patients and their data as well.
Elemer Piros
And would we have some aHUS patients data as well?
Greg Demopulos
At the renal program?
Elemer Piros
Yes.
Greg Demopulos
That well I need to check with our clinical group, I know that aHUS data is coming up later in April at the World Congress.
Operator
Our next question comes from Jason Kolbert from Maxim Group. Your line is now open.
Jason Kolbert
I'd like to talk a little bit about OMS721 particularly as it relates to TMA's and stem cell transplantation. Can you do me a favor and just help me understand kind of the origins of the TMA and kind of what the treatment paradigm would look like for when 721 is going to be used in those patients so I can get a handle on what the market size might be. Thanks.
Greg Demopulos
Right. There's a lot in that question so I'll try to take it in a stepwise progression, Jason. First of all the mechanism, endothelial damage, we believe is the inciting event and endothelial damage activating the lectin pathway specifically. We do know that endothelial damage activates the lectin pathway, we know that MASP-2 is the effector enzyme of the lectin pathway and therefore inhibiting MASP-2 as does OMS721 should have a positive effect in disorders associated or temporarily downstream related to endothelial damage. The endothelial damage in stem cell transplant patients well you know that very well with the conditioning required and the drugs used, both pre and post stem cell transplants, so clearly endothelial damage is there. With respect to what patients specifically the patients who we have treated with OMS721 are those patients who really have severe thrombotic microangiopathy.
So these are patients who are sick very, very sick and these are patients whose mortality rate I think as I mentioned would be expected to be 90% or greater, those are the patients that we are initially treating. With respect to what patient population would be served potentially by OMS721 were clearly those patients. So those patients who have already undergone -- who have TMA's and have undergone revision or modification in calcine urine inhibitors or other immunotherapies and TMA continues certainly those patients are the ones we're treating now.
So I would expect that would be a population amenable to treatment but then I would start to look upstream meaning again temporarily upstream to those patients potentially and again you're asking me and I'm giving you my thoughts I want to be very clear about that but this is a PMA following a stem cell transplant as you know very well is an extremely severe disorder. So could want to imagine moving temporally upstream to those demonstrating changes in any markers of TMA, sure, potentially I could imagine that I think you could too. So with respect to ultimately the population of patients with TMA following stem cell transplant we would treat I think it's likely broader than those patients who we are currently treating now.
Jason Kolbert
So it's sounds like the market initially becomes not quite ultra-orphan but ultra-orphan and I'm assuming ultra-orphan like pricing but eventually it could broaden out that kind of much significantly larger segment of the market.
Greg Demopulos
Yes especially when you think of what other disorders are associated with TMA's. There probably there are over 20,000 stem cell transplants U.S. alone, but then you start to think about the other disorders associated with stem cell transplant and there I'm talking about graft versus host disease or GVHD or of veno-occlusive disease as well and you start to think about, gee, what are their opportunities as well and I can tell you that certainly we are considering those as potential opportunities.
Operator
Thank you. And that completes the Q&A part of the call. I would like to turn the call back over to Dr. Demopulos for closing comments.
Greg Demopulos
Well thank you very much, that ends our call for today and I would like to thank everyone for taking the time to listen in today as I said earlier 2017 promises to hold a series of important milestones throughout the year and we do expect to provide additional information on a number of the programs that we discussed today and perhaps others as the year progresses. As always to each of you we appreciate your continued interest and support. Have a good day and we look forward to talking with you again soon.
Operator
Ladies and gentleman thank you for your participation in today's call. This does conclude the program. You may all disconnect. Everyone have a great day.
Copyright policy: All transcripts on this site are the copyright of Seeking Alpha.
I am re-positioning as I type
will see what earnings bring, before leap
thanks for heads up,
snup
Doc,
thanks I am watching it but over extended right now with my
expendable funds.
snup
Imo Good time to jump aboard for the next 25% run
Quote-Dr. come over to stocktwits and share some of your knowledge. Theres over 2600 omer followers there--
Been 2600 for a few months but ran to 2800 in 2 weeks time, posting there since the day you recomended it.
Gr
Kreftslag
I would have held untill financials monday morning, gonna run another week if me break 15mil this Q
Untill sequestox or blockbuster approval Averaging down on elite is IMHO a waste of those profits you made here
GL
Wow,
Data indeed came in!
talk about bad timing!
Great news for you Doc,
snup
Doc,
Its been a decent run, had to sell my other 2500
a little over 7k profit, eltp ouch! but this may
prove to be the month to average down Linc. concludes
in april I believe.
Snup
will come back if omer drops again , and with bio world
very possible, data may prove me wrong, but had to get
some green for a change, still waiting on others to move.
snup
Doc,
thanks for advise,
look at rxmd, now bouncing off 52 week lows
best to you,
snup
No i did not listen to eltp's CC
there will be no surprises this year
Imo more dilution and slow growing revenues will make elite a 8 cent stock before sequestox is approved
If ever approved i'll jump on board again. But the longer i'm away from elite, the less attractive it seems
its imho dead money for at least another year
Untill approval I'll just keep trading omer , pgnx and clvs
Good luck
sold my 2200 shares, will ride my others
readying to buy you know what Doc.
Are you gonna listen monday?
snup
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http://www.omeros.com/
http://finance.yahoo.com/q/ks?s=OMER+Key+Statistics
Omeros is a Seattle-based biopharmaceutical company committed to discovering, developing, and commercializing small-molecule and protein therapeutics for large-market as well as orphan indications targeting inflammation, coagulopathies, and disorders of the central nervous system. Our most advanced product candidates are derived from our proprietary PharmacoSurgery® platform designed to improve clinical outcomes of patients undergoing ophthalmological, arthroscopic, urological and other surgical and medical procedures. Our PharmacoSurgery platform is based on low-dose combinations of therapeutic agents delivered directly to the surgical site throughout the duration of the procedure to inhibit preemptively inflammation and other problems caused by surgical trauma and to provide clinical benefits both during and after surgery. Omidria™ (phenylephrine and ketorolac injection) 1%/0.3%, the first commercial product from Omeros’ PharmacoSurgery platform, was approved by the FDA in May 2014. Omidria is also currently under review for marketing approval by the European Medicines Agency (EMA). Omeros’ six other clinical programs are focused on schizophrenia, Huntington’s disease, and cognitive impairment; addictive and compulsive disorders; complement-related diseases; and preventing problems associated with surgical procedures. Two additional programs are expected to advance into the clinic next year – one for the control of blood loss during surgery or resulting from trauma and the second for the treatment of a wide range of addictions and compulsions as well as any movement disorder. Omeros also has a proprietary GPCR platform, which is making available an unprecedented number of new GPCR drug targets and corresponding compounds to the pharmaceutical industry for drug development. | ![]() |
Omeros is developing a deep pipeline of small-molecule and protein therapeutic candidates targeting inflammation, coagulopathies, and disorders of the central nervous system. Our twelve programs include those focused on inflammation, coagulopathies, and multiple CNS disorders, as well as our three platform programs: PharmacoSurgery®, antibody and G protein-coupled receptor all targeting both large-market and exciting orphan opportunities. Products from our proprietary PharmacoSurgery platform, which yielded our first commercial product Omidria™ (phenylephrine and ketorolac injection) 1%/0.3%, for use during cataract surgery and other lens replacement procedures, are designed to improve the clinical outcomes of patients undergoing arthroscopic, urological, and other surgical and medical procedures. Our MASP program is in clinical development to treat thrombotic microangiopathies, including atypical hemolytic uremic syndrome, and a wide range of inflammatory disorders. Our two PDE10 clinical programs for the treatment of schizophrenia and Huntington's disease, our clinical program for the treatment and prevention of addictions and compulsions and our preclinical programs targeting other CNS disorders and coagulopathies further strengthen our pipeline and help create multiple opportunities for commercial success. Our GPCR platform is making available an unprecedented number of new GPCR drug targets and corresponding compounds to the pharmaceutical industry for drug development, and our antibody platform enables the discovery of novel, high-affinity monoclonal antibodies. For each of our product candidates and programs, we have retained all manufacturing, marketing and distribution rights. | ![]() | |
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Our proprietary PharmacoSurgery® products are designed to improve the clinical outcomes of patients undergoing ophthalmological, arthroscopic, urological and other surgical and medical procedures. Omidria™ (phenylephrine and ketorolac injection) 1%/0.3%, is the first approved drug from our PharmacoSurgery platform |
![]() | We have multiple programs focused on central nervous system (CNS) disorders, all targeting large markets. Our most advanced CNS programs include our phosphodiesterase 10 (PDE10) program, focused on developing drugs for the treatment of schizophrenia, Huntington's disease and other cognitive disorders; our PPARγ program, focused on developing proprietary compositions that include peroxisome proliferator-activated receptor gamma (PPARγ) agonists for the treatment and prevention of addiction to substances of abuse (e.g., opioids, nicotine and alcohol); and our PDE7 program for the development of drugs for the treatment of movement disorders, such as Parkinson's d |
![]() | We are developing antifibrinolytic agents for the control of blood loss during surgery or resulting from trauma. Excessive bleeding during cardiac surgery is known to increase overall morbidity and mortality. In an attempt to control this bleeding, patients undergoing cardiac and other extensive surgery often receive antifibrinolytic compounds. These drugs inhibit plasmin, an enzyme present in blood that degrades fibrin clots. Because plasmin degrades fibrin clots, an agent that inhibits plasmin may have potential utility for reducing blood loss due to trauma or surgery. Prior to withdrawal from the market in 2008 for safety concerns, the antifibrinolytic Trasylol® (aprotinin) had been shown in a number of studies to be more effective at reducing blood loss than the other two most commonly used antifibrinolytics on the market today, tranexamic acid and epsilon aminocaproic acid. While Trasylol® is a potent inhibitor of plasmin, it is non-selective. In addition to plasmin, it significantly inhibits kallikrein and Factor XIa, two enzymes important in promoting clotting, and their inhibition can increase bleeding. Trasylol® was found to be associated with a number of safety issues, including increased mortality. Further, it is a bovine protein associated with anaphylactic reactions. While the specific cause of increased death remains unknown, an often-cited explanation is the lack of specificity of Trasylol®. Our proprietary agents also inhibit plasmin but, unlike Trasylol®, they do not significantly inhibit kallikrein and Factor XIa. Additionally, our agents are derived from human protein, which may reduce immunological side effects. The properties of our proprietary agents are described in a peer-reviewed article titled "Engineering Kunitz Domain 1 (KD1) of Human Tissue Factor Pathway Inhibitor-2 to Selectively Inhibit Fibrinolysis: Properties of KD1-L17R Variant" that was published in the February 11, 2011 issue of the Journal of Biological Chemistry. We believe the efficacy and improved selectivity of our proprietary agents provide a novel approach to the control of bleeding from surgery and trauma. We have selected a lead clinical candidate and are manufacturing pre-clinical supplies to enable the initiation of GLP toxicology studies intended to support the submission of an IND or clinical trial application and subsequent clinical trials. We plan to be in clinical trials with our anti-plasmin molecule in 2015. Patent Position As of February 15, 2014, we owned one issued patent and three pending patent applications in the U.S. and seven issued patents and 26 pending patent applications in foreign markets directed to our recent discoveries linking PPAR? and |
![]() | G protein-coupled receptors (GPCRs), which mediate key physiological processes in the body, are one of the most valuable families of drug targets. According to Insight Pharma Reports, GPCR-targeting drugs represent 30 to 40 percent of marketed pharmaceuticals. Examples include Claritin® (allergy), Zantac® (ulcers and reflux), OxyContin® (pain), Lopressor® (high blood pressure), Imitrex® (migraine headache), Reglan® (nausea) and Abilify® (schizophrenia, bipolar disease and depression) as well as all other antihistamines, opioids, alpha and beta blockers, serotonergics and dopaminergics. The industry focuses its GPCR drug discovery efforts mostly on non-sensory GPCRs. Of the 363 total non-sensory GPCRs, approximately 240 have known ligands (molecules that bind the receptors) with nearly half of those targeted either by marketed drugs (46 GPCRs) or by drugs in development (about 70 GPCRs). There are approximately 120 GPCRs with no known ligands, which are termed "orphan GPCRs." Without a known ligand, drug development for a given receptor is extremely difficult. Omeros uses its proprietary high-throughput cellular redistribution assay (CRA) to identify small-molecule agonists and antagonists for orphan GPCRs, unlocking them to drug development. Omeros believes that it is the first to possess the capability to unlock orphan GPCRs in high-throughput, and that currently there is no other comparable technology. Unlocking these receptors could lead to the development of drugs that act at these new targets. There is a broad range of indications linked to orphan GPCRs including cardiovascular disease, asthma, diabetes, pain, obesity, Alzheimer's disease, Parkinson's disease, multiple sclerosis, schizophrenia, learning and cognitive disorders, autism, osteoporosis, osteoarthritis and several forms of cancer. Omeros has begun screening orphan GPCRs against its small-molecule chemical libraries using its proprietary, high-throughput CRA. In addition to Class A orphan GPCRs, we have also begun screening orphan and non-orphan Class B receptors. Class B GPCRs have large extracellular domains and their natural ligands are generally large peptides, making the development of orally active, small-molecule drugs against these receptors, such as glucagon and parathyroid hormone, a persistent challenge. Omeros has announced that it has identified and confirmed sets of compounds that interact selectively with the following orphan receptors: | ![]() | ![]() | ![]() | The GPCR family represents an important source of drug discovery. Of the 363 characterized GPCRs, only about 46 are currently targeted by marketed drugs, yet GPCR-targeted drugs account for 30-40% of all drugs sold worldwide. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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![]() | In parallel, Omeros is executing on its intellectual property strategy to protect each unlocked target through a multipronged approach directed to compound structures, uniquely identified signaling pathways and associated therapeutic indications. Collectively, this approach provides Omeros the opportunity to establish broad and enforceable protection for each unlocked receptor. GPR17We are optimizing compounds against GPR17, a G protein-coupled receptor (GPCR) which is linked to myelin formation. Myelin is an insulating layer rich in lipids and proteins that forms a sheath around the nerve fibers, which is essential for the proper functioning of the nervous system. Loss of the myelin sheath is the hallmark of several diseases, including multiple sclerosis, acute disseminated encephalomyelitis, Neuromyelitis Optica, transverse myelitis, chronic inflammatory demyelinating polyneuropathy, Guillain-Barré syndrome, central pontine myelinosis, inherited demyelinating diseases such as leukodystrophy, and Charcot-Marie-Tooth disease. We believe GPR17 inhibitors have the potential to promote remyelination and improve the outcome of these diseases as well as traumatic brain injury and spinal cord injury, conditions that have been associated with GPR17. Discovering GPR17 inhibitors has previously been challenging to the pharmaceutical industry because this receptor is an orphan GPCR. However, using our proprietary CRA, we have been able to identify over 100 compounds that functionally interact with GPR17. We are now in the process of developing lead molecules targeting GPR17, which we intend to evaluate in remyelination assays in cell culture systems as well as in animal models. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
![]() | Patent Position As of February 15, 2014, we owned five issued patents and 10 pending patent applications in the U.S., and 43 issued patents and eight pending patent applications in foreign markets , which are directed to previously unknown links between specific molecular targets in the brain and a series of CNS disorders, our cellular redistribution assay and other research tools that are used in our GPCR program and to orphan GPCRs and other GPCRs for which we have identified functionally interacting compounds using our cellular redistribution as |
![]() | Our proprietary ex vivo platform for the discovery of novel, high-affinity monoclonal antibodies utilizes a chicken B-cell lymphoma cell line and has demonstrated potential for the generation of diverse antibodies that can be readily engineered. This platform offers several advantages over other antibody platforms. The ex vivo immunizations of our proprietary cell line are significantly more rapid than whole animal immunizations and conventional hybridoma technology. By avoiding immunization of mice or other animals, we believe that the antibodies we generate from this platform are not limited by immunological tolerance. Our platform is capable of producing novel antibodies against difficult targets, such as highly homologous proteins, enzymes, and receptors with short extracellular domains. Chicken antibodies also have unique features that enable binding capabilities distinct from mammalian antibodies. We have generated antibodies to several clinically significant targets, and our platform continues to add antibodies against additional important targets to our pipeline. Patent Position As of February 15, 2014, we owned and/or held worldwide exclusive license rights from the University of Washington to three pending U.S. Patent Applications, four foreign patent applications and one International Patent Cooperation Treaty Patent Application directed to our antibody platform. Additionally, we owned one issued U.S. Patent, two pending U.S. Patent Applications and eight pending foreign applications directed to antibodies generated |
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