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well.... hasn't been great.... but as of late... money to be made buying on dips and then selling close in options... like at if next Friday still above I'll be making 12-15% on stock I bought .... some will only be about 2 weeks old.... these were extra shares bought believing it will be 5 next week.... wish I even bought more... do have some that I covered with June 6s and 7s that could work out good!! Bulk waiting for a good move up from here!!
Good luck!! Earnings on 15th
Could this has traded poorly since the announcement. Disappointed. Dilution could be the reason and market not happy about extended time frame.
I really don't like playing this "when will it be approved game" cause everyone gets too ramped up about made-up timelines. The company didn't really guide anything specific, and didn't leave room for error. For instance, API supplier #1 provided FDA responses and changes, but that doesn't mean FDA accepted. With that said, the absolute best case scenario I saw was (assuming everything goes well), is possible approval in September. Request meeting mid March, FDA responds early April (14 days), Meeting early May (30 days), prepare and resubmit NDA class 2 early to Mid July (2 months rough estimate not guided), FDA approves early to mid September (60 days). This is best case and assumes no new on site inspection of existing manufacturer. If inspection is required, move from Q3 to Q4. As far as new CMO, figure summer 2024. My best guess and I am no pro. Good luck.
News out AH today that the primary CMO has completed the corrective actions from the FDA
2022 inspection. Anyone now how soon now until approval or when the FDA will
reinspect the CMO facility and assuming it passes, how long until FDA approves?
Moving nice today!!! Up 7.41%!! Have another much hotter today ... but with the target here Happy to see it moving.... just Sold March 6s options. Love to see them take it from me at that price in 17 days!!! Have more not optioned!! They need $6.10 just to break even!!
Great day today.... well so far!!
Let's hope Joe can get this across the finish line.
Slowly creeping back up...... trying to. Just a little today .... hoping for lunch time pull back....
Price far below JMP target of 14 !!!
CRMD broke over 4 today!!! Nice move....
reslabrat...thanks for the info...and best of luck to all
Yeah, saw that. Good news for sure. Hoping we can finally get past that FDA hurdle and we are golden
NTAP Approval
This was posted today in the CMS FY 2023 Hospital Inpatient Prospective Payment System (IPPS) and Long-Term Care Hospital Prospective Payment System (LTCH PPS) Final Rule — CMS-1771-F Aug 01, 2022 Medicare Parts A & B.
"Applications for NTAP Approved for FY 2023"
"CMS also conditionally approved one technology under the alternative pathway for products that received FDA Qualified Infectious Disease Product (QIDP) designation that otherwise meets the alternative pathway criteria, but has not yet received FDA approval."
Maybe this is the NTAP approval for Defencath.
great news today...i bot more....burp
to me its a slam dunk...all in my opinion
just makes sense.
best to all
Company announced resubmission of defencath NDA this morning. No reason this should be under 10. Are their any short positions?
CorMedix to Participate in Upcoming January Conferences
BERKELEY HEIGHTS, N.J., Jan. 04, 2022 (GLOBE NEWSWIRE) -- CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, today announced that CorMedix management will be participating in several upcoming investor conferences in January.
Investor Conference Details
LifeSci Partners – 11th Annual Corporate Access Event
Wednesday, January 5th – Friday, January 7th
To register and submit one-on-one meeting requests, Click Here
H.C. Wainwright Bioconnect Virtual Conference
Monday, January 10th – Thursday, January 13th
To register for the conference, Click Here
Biotech Showcase Virtual Conference
Monday, January 10th – Wednesday, January 12th
To register and submit one-on-one meeting requests, Click Here
About CorMedix
CorMedix Inc. is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory diseases. The Company is focused on developing its lead product DefenCath™, a novel, antibacterial and antifungal solution designed to prevent costly and life-threatening bloodstream infections associated with the use of central venous catheters in patients undergoing chronic hemodialysis. DefenCath has been designated by FDA as Fast Track and as a Qualified Infectious Disease Product (QIDP), and the NDA received priority review in recognition of its potential to address an unmet medical need. QIDP provides for an additional five years of marketing exclusivity, which will be added to the five years granted to a New Chemical Entity upon approval of the NDA. CorMedix also committed to conducting a clinical study in pediatric patients using a central venous catheter for hemodialysis when the NDA is approved, which will add an additional six months of marketing exclusivity when the study is completed. The Company received a Complete Response Letter from FDA stating that the NDA could not be approved until satisfactory resolution of deficiencies at the contract manufacturing facility, including in-process controls for the filling operation. CorMedix also intends to develop DefenCath as a catheter lock solution for use in oncology and total parenteral nutrition patients. It is leveraging its taurolidine technology to develop a pipeline of antimicrobial medical devices, with programs in surgical sutures and meshes, and topical hydrogels. The Company is also working with top-tier researchers to develop taurolidine-based therapies for rare pediatric cancers. Neutrolin® is CE Marked and marketed in Europe and other territories as a medical device. For more information, visit: www.cormedix.com.
Investor Contact:
Dan Ferry
Managing Director
LifeSci Advisors
(617) 430-7576
At some point this will be FDA approved..the need for the product is off the map..the question remains..wtf is holding this up?
The stock was upgraded to 32 dollars just before the FDA approval was to be granted..Hoping for 12 dollars on a buyout is ridiculous.
Patience will pay off here.
As I said a few days ago..this is when you should be adding...not talking about selling the company for 12 a share..lol
Hopefully..we'll get an update with some positivity in it...there is an acute need for their products...this is taking so damn long to get FDA approval...
Grease the palms..let's get this done.
CorMedix Inc. to Report Third Quarter 2021 Financial Results and Provide a Corporate Update on November 9
BERKELEY HEIGHTS, N.J., Nov. 02, 2021 (GLOBE NEWSWIRE) -- CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, today announced that it will report its financial results for the third quarter ended September 30, 2021, after the market close on Tuesday, November 9, 2021, and will host a corporate update conference call at 4:30pm Eastern Time.
Tuesday, November 9(th) @ 4:30pm ET
--------------------------------------
Domestic: 877-423-9813
International: 201-689-8573
Conference ID: 13723602
I hope the CRMD BOD decides to place the company up for sale so the
production, marketing, and sales of this life-saving product can be
done by management that actually know what they are doing...I'd rather
take $12 today than have to wait years for a uncertain amount way out
in the future. Meanwhile, each day that goes by is one less day of
patent life protection.
Good Riddance to the CEO...Hope the interim CEO will consider selling
the company NOW instead of hiring a new CEO. One would think someone
on the BOD would have connections to initiate some interest by a BP
that could perhaps even manufacture the product themselves!
The bigger issue is IF this CMO doesn't get its act together (reg compliance), it could lose its fDA cert to be a CMO...
But as someone who has done 'supplier' qualifying audits, there are all kinds of 'things' that can go wrong..
The question is, what are the 'issues', and are they in the category of, we can't manufacture anything cause we can't be trusted to put out a quality product..
On the other hand, it could be that CRMD is staying one step ahead of the ambulance chasing so called 'legal' firms by being over cautious to not give them any reason to 'sue' (to line their pockets while claiming to care about the little 'shareholders')
yaafah...i totally agree....sad
This announcement today of a further delay with no details is BULLSHIT!
It's like the company is intentionally driving the stock price into the gutter.
Read this BS...no details.
CorMedix Inc. Announces Regulatory Update
BERKELEY HEIGHTS, N.J., Sept. 07, 2021 (GLOBE NEWSWIRE) -- CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, today provided an update with respect to its resubmission timeline for the DefenCath New Drug Application (“NDA”). CorMedix has encountered delays at its third-party contract manufacturer (“CMO”). The Company was informed by the CMO that there are issues that are unrelated to DefenCath manufacturing activities. The timeline for CorMedix and the CMO to address deficiencies at the facility that are required for resubmission of the DefenCath NDA is uncertain at this time. We will provide an update when more information becomes available.
About CorMedix
CorMedix Inc. is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory diseases. The Company is focused on developing its lead product DefenCath™, a novel, antibacterial and antifungal solution designed to prevent costly and life-threatening bloodstream infections associated with the use of central venous catheters in patients undergoing chronic hemodialysis. DefenCath has been designated by FDA as Fast Track and as a Qualified Infectious Disease Product (QIDP), and the NDA received priority review in recognition of its potential to address an unmet medical need. QIDP provides for an additional five years of marketing exclusivity, which will be added to the five years granted to a New Chemical Entity upon approval of the NDA. CorMedix also committed to conducting a clinical study in pediatric patients using a central venous catheter for hemodialysis when the NDA is approved, which will add an additional six months of marketing exclusivity when the study is completed. The Company received a Complete Response Letter from FDA stating that the NDA could not be approved until satisfactory resolution of deficiencies at the contract manufacturing facility, including in-process controls for the filling operation. CorMedix also intends to develop DefenCath as a catheter lock solution for use in oncology and total parenteral nutrition patients. It is leveraging its taurolidine technology to develop a pipeline of antimicrobial medical devices, with programs in surgical sutures and meshes, and topical hydrogels. The Company is also working with top-tier researchers to develop taurolidine-based therapies for rare pediatric cancers. Neutrolin® is CE Marked and marketed in Europe and other territories as a medical device. For more information, visit: www.cormedix.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to risks and uncertainties. All statements, other than statements of historical facts, regarding management’s expectations, beliefs, goals, plans or CorMedix’s prospects, future financial position, financing plans, future revenues and projected costs should be considered forward-looking. Readers are cautioned that actual results may differ materially from projections or estimates due to a variety of important factors, including: the results of our discussions with the FDA regarding the DefenCath development path for marketing authorization; the resources needed to secure approval of the new drug application for DefenCath from the FDA; the risks and uncertainties associated with CorMedix’s ability to manage its limited cash resources and the impact on current, planned or future research, including the continued development of DefenCath/Neutrolin and research for additional uses for taurolidine; obtaining additional financing to support CorMedix’s research and development and clinical activities and operations; preclinical results are not indicative of success in clinical trials and might not be replicated in any subsequent studies or trials; and the ability to retain and hire necessary personnel to staff our operations appropriately. We continue to assess to what extent the uncertainty surrounding the Coronavirus pandemic may impact our business and operations. These and other risks are described in greater detail in CorMedix’s filings with the SEC, copies of which are available free of charge at the SEC’s website at www.sec.gov or upon request from CorMedix. CorMedix may not actually achieve the goals or plans described in its forward-looking statements, and investors should not place undue reliance on these statements. CorMedix assumes no obligation and does not intend to update these forward-looking statements, except as required by law.
Investor Contact:
Dan Ferry
Managing Director
LifeSci Advisors
(617) 430-7576
That was 5 months ago...
CRMD presents next wed. 4/14.... likely to get update on delay imo.
CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, today announced that CorMedix management will present a corporate overview at the 20th Annual Needham Virtual Healthcare Conference taking place on April 12 – 15, 2021.
20th Annual Needham Virtual Healthcare Conference (virtual)
Date: Wednesday, April 14th
Time: 4:30 pm Eastern Time
Webcast: https://wsw.com/webcast/needham107/crmd/2235068
CRMD nice move today..... gap to fill in teens if she can close above 10.
Looks likely no meeting, only a couple month delay. CRMD now technically has a gap to fill. Worst over here.
The actions CorMedix ( CRMD ) needs to take to address deficiencies flagged by the FDA in its recent rejection of the company's application for its DefenCath catheter-lock solution are manageable and will likely result in a quick resolution, Truist reckons. CorMedix ( CRMD ) is targeting a May refiling with the FDA, and Truist says it believes a "Class 1" resubmission is likely, given that the FDA concerns weren't linked to the safety and efficacy of the product but rather issues at the contract manufacturer. A Class 1 response would mean a two-month review, with an FDA decision by July, the firm says.
Laz...thanks for your input...greatly appreciated and best to you
It will drop to between $5-$6 before FDA meeting in April.
We'll see.
The meeting with FDA is in April. and CRMD needs to work on the changes. And FDA needs to take another 2-3 months to respond. YOU WILL SEE IT.
Been long 4 years and will stay long, but not blind to the reality that there is a bear and a bull case here.
FDA says they want more info from manufacturer and a manual study to make sure right amount of defencath is extracted from viles. Without a CC we are left to guess what that means. My assumption is the manufacturer didn't provide a strong enough case that their control procedures are in place to ensure proper vile fill up. So FDA says prove you are putting the right amount in each vile and then prove there is a back up by ensuring the proper amount is extracted for use so we are sure the manufacturer isn't shorting or overfilling viles.
Just my guess.
My thoughts:
1. Easy fix for sure
2. Easy doesn't mean quick. It takes 45 days just to schedule a meeting.
3. That April meeting is REALLY important. There is a chance CRMD will need to remedy the issues and then file a new NDA. This is worst case scenario. That get us to Q4 2021 / Q1 2022.
4. Best case is Q3 2021. Without a whole new NDA filing.
5. Capitol Raise..... probably not, but they really like that ATM. IF a new NDA is needed, that is bad! They would need money. This is where investors struggle. When a company says they have enough money for 1 year, they need to raise pretty quick. Can't run the bank account to zero.
4. I am figuring in about a 10% dilution now into my own spreadsheet I keep by Q1 2022.
5. The bulls have had control of the price the past few weeks, now control appears to be with day traders. If control move to bears, look out.
6. $8-9 is a good buy in my opinion, but would not be surprised if it goes down more.
7. I am thinking short term (1-6) month bear case and long term bull case as of this minute. CRMD management can change my opinion with a simple conference call.....but the lack of a call signals a lack of a plan.
8. Then again, I could be full of crap and they fix everything in 2 months and we are off to the races......this would be fantastic! Still long, will buy more at some point.
Final note from me:. Really disappointed with the company. They took their time with the excuse of crossing all t's and dotting all I's yet here we are. These are my opinions only.
Dr. Balauh has already pointed out that they have $88 million in funds on the books to cover operations until Q42022--stop this "dilution" baloney already-and approval will be later this year--why would a manufacturing glitch take a whole year to settle (COVID or no COVID)
Manufacturer & label issue will take at least 6-12 months to resolve.
I think another PUFTA date in February, 2022. In this case, yes. company will dilute again later this year (most likely 4th quarter this year).
Good point..I took advantage of the selloff and more than doubled my position today...the wild card is we don't really know how long we'll have to hold to capitalize on DefenCath.
It bothers me that it is approved for use outside of the USA....and at the 23rd hour this glitch magically appears....right before FDA approval here.
I am having a hard time blaming the company for this.
I personally believe this is FDA meddling for whatever reason.
Don’t discourage maybe we’ll get some more stupid selling tomorrow morning. Guys like this are our friends :)
* * $CRMD Video Chart 03-01-2021 * *
Link to Video - click here to watch the technical chart video
Did you even read the press release?
This is right out of it:
"CorMedix ended the 4th quarter of 2020 with pro forma cash, cash equivalents and short-term investments of approximately $87.8 million, including capital raised though ATM issuance, which the company estimates is sufficient to fund operations at least into second half of 2022."
Why are you talking about dilution right now?
Ridiculous.
CRMD will have another dilution before FDA approval. Approval might come in year 2022. Forget about this year...
and what is the likelihood the company has the funds to get to approval now without another crummy dilution?? I'm staying on the "sidelines" about buying more shares--if I buy 1000 SHARES I bought 1000 shares--PERIOD--I'm not going to bother with 100 or 50 shares after another dilution
There is nothing wrong with DefenCath..it's the delivery system...and the manufacturer....
This is on Cormedix...they should have made sure everything was proper.
Now this whole process will be delayed.... and further delayed because of
Covid and the backlog the FDA needs to get through.
I just took advantage of the opportunity to double my position.
Not giving up on this ticker by any stroke of the imagination.
But a delay is inevitable now.
Meeting requested with the FDA in April sometime.
Was expecting some kind of announcement today on the FDA filing...so far nothing and the share price is getting pummeled once again.....go figure.
Guess the market makers want to see how much pain we're prepared to endure.
I'm not selling.
BlackRock Inc. ownership in CRMD / CorMedix Inc.
2021-01-29 - BlackRock Inc. has filed an SC 13G/A form with the Securities and Exchange Commission (SEC) disclosing ownership of 1,995,193 shares of CorMedix Inc. (US:CRMD). This represents 6.2 percent ownership of the company. In their previous filing dated 2020-02-07, BlackRock Inc. had reported owning 1,712,901 shares, indicating an increase of 16.48 percent.
Kind of hoping they announce tomorrow as the 28th is a sunday.
Usually this is what happens.
That would be sweeeet!
We should be able to hit a high of 42.00
I think we hit 30's...imo.
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