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Good point señor.
It's a corporate presentation. Don't hold your breath imo
I got some 74s
Soligenix Phase 2 Data For Oral Mucositis Drug SGX942 Due Soon
November 3, 2016
sngx-pipeline
Pardon me for being a bit impatient and also excited, but Soligenix is due to publish their long term data for SGX942 intended to treat Oral Mucositis in the next 60 days. If the long term data matches the preliminary data, things could get very exciting for this little biotech company that has a billionaire investor in RJ Kirk.
SGX942, a first-in-class Innate Defense Regulator (IDR), at a dose of 1.5 mg/kg, successfully reduced the median duration of severe oral mucositis by 50% in all patients and by 67% in patients receiving the most aggressive chemoradiation therapy (CRT) for treatment of their head and neck cancer.
This exploratory study achieved all objectives, including identifying a best dose of 1.5 mg/kg. The study enrolled 111 patients across three SGX942 dose groups (i.e., 1.5, 3.0, and 6.0 mg/kg) and a placebo group and evaluated patients undergoing CRT for head and neck cancer. In the 1.5 mg/kg treatment group, the median duration of severe oral mucositis was decreased by 50%, from 18 days to 9 days (p=0.099), meeting the prospectively defined statistical threshold of p<0.1 in the study protocol. Further, patients receiving the most aggressive CRT in this dose group had even more striking reductions in their median duration of severe oral mucositis of 67%, from 30 days to 10 days (p=0.040). Clinicians are most concerned about severe oral mucositis, which includes patients who cannot eat and/or drink due to their mouth ulcers.
In addition to the oral mucositis findings, a trend towards increased incidence of “complete response” of tumor at the one month follow up visit was observed (47% in placebo vs. 63% in SGX942 at 1.5 mg/kg). Decreases in mortality and significant decreases in infection rate were also observed with SGX942 treatment and are being further evaluated. In the preliminary analysis, SGX942 was found to be generally safe and well tolerated, consistent with the safety profile observed in the prior Phase 1 study conducted in 84 healthy volunteers. Long-term follow-up evaluations are ongoing with final results expected in the fourth quarter of 2016. Data from this Phase 2 trial is expected to be submitted for future presentation and publication.
One of the leading investigators in oral mucositis, Stephen T. Sonis, DMD, DMSc, Professor of Oral Medicine at Harvard School of Dental Medicine and Member of the Soligenix Oral Mucositis Medical Advisory Board noted, “Oral mucositis is a devastating side effect of CRT used for the treatment of head and neck cancers, which compromises patients’ tolerability of therapy and quality of life, and adds to health and economic burdens associated with care. Despite intense efforts to develop effective interventions for CRT-induced mucositis, there are currently no approved drugs. SGX942 is the first Innate Defense Regulator in development for oral mucositis. The favorable results noted in this trial demonstrate the validity of a novel treatment approach which targets critical biological events leading to mucositis and strongly support further trials. The clinical results are consistent with preclinical animal studies in which SGX942 reduced duration of oral mucositis by approximately 50% following either chemotherapy or radiation therapy.”
“We are extremely pleased with the findings from the first Phase 2 study of SGX942. The study met all of its objectives of defining the best dose, the most appropriate clinical endpoint, and patient population to use in future pivotal trials,” stated Richard Straube, MD, Senior Vice President and Chief Medical Officer of Soligenix. “The positive and clinically meaningful effect observed on the duration of ulcerative and severe oral mucositis clearly demonstrates the significant biologic activity that SGX942 exerts on this catastrophic side-effect of cancer treatment. The impact of SGX942 on other clinically beneficial outcomes (e.g., tumor control and infection rates) confirms the animal model data that, in treating patients’ oral mucositis, SGX942 may also prove to have a positive impact on their head and neck cancer.”
“After years of development, it is truly gratifying to witness this transformational event, in which the potential of the IDR technology begins to be translated into the clinical setting,” stated B. Brett Finlay, PhD, University of British Columbia, Peter Wall Distinguished Professor, CIFAR Senior Fellow Michael Smith Laboratories and co-founder of the IDR technology. “With their unique mechanism of action, IDRs have the potential to not only mitigate oral mucositis, but also address the increasing problem of emerging and antibiotic resistant bacterial infections.”
“We are very excited with the outcome of this Phase 2 clinical study,” stated Christopher J. Schaber, PhD, President and Chief Executive Officer of Soligenix. “Given the positive and compelling preliminary data generated in oral mucositis, where there is substantial market potential, we will now look to engage the US Food and Drug Administration (FDA) on the size and scope of a pivotal Phase 2/3 clinical program since the data suggest that a pivotal trial could potentially be designed of a size roughly similar to the completed trial. Simultaneous with this activity, we will be aggressively pursuing opportunities for partnership to support subsequent clinical trials with SGX942. With the biologic activity of the IDR technology now confirmed in humans, we will also look to expand its potential utility in the infectious disease space.”
Dr. Schaber continued, “With the successful completion of the Phase 2 oral mucositis study, we now direct clinical efforts to the quality execution of our pivotal Phase 3 clinical trial in cutaneous T-cell lymphoma (CTCL) with SGX301, which was recently opened for enrollment. CTCL is a high priority disease indication, having received fast track and orphan designation from the FDA, and has the potential to support marketing registration in the US and the rest of the world.”
The clock is ticking and my fingers are crossed that the preliminary data and long term data match. Dr. Christopher Schaber (CEO of Soligenix) stated that he believed the Net Present Value of SGX942 alone was $100M or greater. That was back in April of this year. With positive long term data it seems reasonable to assume the net present value of SGX942 may be greater than $100M which means there is at least 7x upside from the current $15M market cap the company has now. Fingers crossed…
Article link - http://sylvacap.com/soligenix-phase-2-data-oral-mucositis-drug-sgx942-due-soon
Form 4 out AH: Randal Kirk got his 2.1M preferred shares converted to 428K common stock. http://app.quotemedia.com/data/downloadFiling?webmasterId=91030&type=PDF&ref=11238932
Nice close today. Based on the fifth amendment to S1 that was filed today, they've remained constant in number of warrants from S1 amend 4 but have gone up from the second amendment. It will not matter in the short term imo if the exercise price for warrants is much higher than current pps. Also remains to be seen what price they'll do the offering at for the combined share + warrant offering.
I see bid creeping up. That's your signal to start covering.
Exactly right señor Theo. Glty
I've found it's best to slap the ask of serious about picking shares here. They're not available as much. Lot of prints by MMs but may not be actual trades?
MMs seem to be putting up fake ask walls imo. I just broke through 25K shares on ask at 90¢ by a 500 share slap. Clowns.
How clever. How's that working for you in general.
No play for me there. It's junk company imo.
And you know this how? Lmfao
On the move today. Want to see that dollar break
Hey you don't want to dump into that 2.95 bid?
Don't wait too long imo. Chart is crazy oversold and co may announce Nasdaq uplist or any other catalyst anytime. Float is so tiny you won't get these prices if she starts moving. Also nothing says sgx 942 update may not come this month. My two cents.
I'm adding too.
Lol maps. Good to hear from you. Was getting lonely on this board as the sole long here
This is what caught my eye from the ER
You should go short again. This thing is going to zero right? About $3 or so of gain per share. No?
And did you say we were going up this week? What you're a long now? Lmfao
I've got you on un-ignore for now. Since no one else is talking to me lmao. So be on your best behavior. L
Why would I initiate a long position here if I knew you were right. Makes no sense to me
That's like a weeks worth of volume. Who is holding the stock down if it were not the warrants
Lmao. I'm not going to bother putting some sense into you.
This one is a phase III company with 12M MC and 3.4M shares OS/2.4M float. Enough said.
Nice news. Pps still in the toilet. Waiting for data
Also maybe you missed this part of the company update:
You want the company to announce partnership before deal is done? Ok!
And then this is what you pulled on me
I don't think they'll do a raise at these levels. Remember the last S3 was done around June at $2.35/share. Also they've an S1 on file so will likely use that vs doing a separate raise imo. Unless the pps goes to like $5 based on the trials data and then they do another raise. I'll be very ok with that.
Soligenix $SNGX
Soligenix Phase 2 Data For Oral Mucositis Drug SGX942 Due Soon
By Ross Silver - November 3, 2016
Link: http://sylvacap.com/soligenix-phase-2-data-oral-mucositis-drug-sgx942-due-soon
Pardon me for being a bit impatient and also excited, but Soligenix is due to publish their long term data for SGX942 intended to treat Oral Mucositis in the next 60 days. If the long term data matches the preliminary data, things could get very exciting for this little biotech company that has a billionaire investor in RJ Kirk.
SGX942, a first-in-class Innate Defense Regulator (IDR), at a dose of 1.5 mg/kg, successfully reduced the median duration of severe oral mucositis by 50% in all patients and by 67% in patients receiving the most aggressive chemoradiation therapy (CRT) for treatment of their head and neck cancer.
This exploratory study achieved all objectives, including identifying a best dose of 1.5 mg/kg. The study enrolled 111 patients across three SGX942 dose groups (i.e., 1.5, 3.0, and 6.0 mg/kg) and a placebo group and evaluated patients undergoing CRT for head and neck cancer. In the 1.5 mg/kg treatment group, the median duration of severe oral mucositis was decreased by 50%, from 18 days to 9 days (p=0.099), meeting the prospectively defined statistical threshold of p<0.1 in the study protocol. Further, patients receiving the most aggressive CRT in this dose group had even more striking reductions in their median duration of severe oral mucositis of 67%, from 30 days to 10 days (p=0.040). Clinicians are most concerned about severe oral mucositis, which includes patients who cannot eat and/or drink due to their mouth ulcers.
In addition to the oral mucositis findings, a trend towards increased incidence of “complete response” of tumor at the one month follow up visit was observed (47% in placebo vs. 63% in SGX942 at 1.5 mg/kg). Decreases in mortality and significant decreases in infection rate were also observed with SGX942 treatment and are being further evaluated. In the preliminary analysis, SGX942 was found to be generally safe and well tolerated, consistent with the safety profile observed in the prior Phase 1 study conducted in 84 healthy volunteers. Long-term follow-up evaluations are ongoing with final results expected in the fourth quarter of 2016. Data from this Phase 2 trial is expected to be submitted for future presentation and publication.
One of the leading investigators in oral mucositis, Stephen T. Sonis, DMD, DMSc, Professor of Oral Medicine at Harvard School of Dental Medicine and Member of the Soligenix Oral Mucositis Medical Advisory Board noted, “Oral mucositis is a devastating side effect of CRT used for the treatment of head and neck cancers, which compromises patients’ tolerability of therapy and quality of life, and adds to health and economic burdens associated with care. Despite intense efforts to develop effective interventions for CRT-induced mucositis, there are currently no approved drugs. SGX942 is the first Innate Defense Regulator in development for oral mucositis. The favorable results noted in this trial demonstrate the validity of a novel treatment approach which targets critical biological events leading to mucositis and strongly support further trials. The clinical results are consistent with preclinical animal studies in which SGX942 reduced duration of oral mucositis by approximately 50% following either chemotherapy or radiation therapy.”
“We are extremely pleased with the findings from the first Phase 2 study of SGX942. The study met all of its objectives of defining the best dose, the most appropriate clinical endpoint, and patient population to use in future pivotal trials,” stated Richard Straube, MD, Senior Vice President and Chief Medical Officer of Soligenix. “The positive and clinically meaningful effect observed on the duration of ulcerative and severe oral mucositis clearly demonstrates the significant biologic activity that SGX942 exerts on this catastrophic side-effect of cancer treatment. The impact of SGX942 on other clinically beneficial outcomes (e.g., tumor control and infection rates) confirms the animal model data that, in treating patients’ oral mucositis, SGX942 may also prove to have a positive impact on their head and neck cancer.”
“After years of development, it is truly gratifying to witness this transformational event, in which the potential of the IDR technology begins to be translated into the clinical setting,” stated B. Brett Finlay, PhD, University of British Columbia, Peter Wall Distinguished Professor, CIFAR Senior Fellow Michael Smith Laboratories and co-founder of the IDR technology. “With their unique mechanism of action, IDRs have the potential to not only mitigate oral mucositis, but also address the increasing problem of emerging and antibiotic resistant bacterial infections.”
“We are very excited with the outcome of this Phase 2 clinical study,” stated Christopher J. Schaber, PhD, President and Chief Executive Officer of Soligenix. “Given the positive and compelling preliminary data generated in oral mucositis, where there is substantial market potential, we will now look to engage the US Food and Drug Administration (FDA) on the size and scope of a pivotal Phase 2/3 clinical program since the data suggest that a pivotal trial could potentially be designed of a size roughly similar to the completed trial. Simultaneous with this activity, we will be aggressively pursuing opportunities for partnership to support subsequent clinical trials with SGX942. With the biologic activity of the IDR technology now confirmed in humans, we will also look to expand its potential utility in the infectious disease space.”
Dr. Schaber continued, “With the successful completion of the Phase 2 oral mucositis study, we now direct clinical efforts to the quality execution of our pivotal Phase 3 clinical trial in cutaneous T-cell lymphoma (CTCL) with SGX301, which was recently opened for enrollment. CTCL is a high priority disease indication, having received fast track and orphan designation from the FDA, and has the potential to support marketing registration in the US and the rest of the world.”
The clock is ticking and my fingers are crossed that the preliminary data and long term data match. Dr. Christopher Schaber (CEO of Soligenix) stated that he believed the Net Present Value of SGX942 alone was $100M or greater. That was back in April of this year. With positive long term data it seems reasonable to assume the net present value of SGX942 may be greater than $100M which means there is at least 7x upside from the current $15M market cap the company has now. Fingers crossed…
$SNGX To Receive $530,000 In Non-Dilutive Funding Through New Jersey Technology Business Tax Certificate Transfer Program
PRINCETON, N.J., Oct. 17, 2016 /PRNewswire/ -- Soligenix, Inc. (OTCQB: SNGXD) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need, announced today that it has received preliminary approval for an approximate $570,000 tax credit from the New Jersey Economic Development Authority's (NJEDA) New Jersey Technology Business Tax Certificate Transfer (NOL) program. As a result, the Company anticipates being able to transfer this credit and receive approximately $530,000 in cash by year end.
This competitive program enables approved technology and biotechnology businesses to sell their unused Net Operating Loss (NOL) Carryovers and unused Research and Development (R&D) Tax Credits to unaffiliated, profitable corporate taxpayers in the state of New Jersey. This allows businesses with NOLs to turn their tax losses and credits into cash proceeds to fund additional R&D, purchase equipment and/or facilities, or cover other allowable expenditures. The NJEDA determines eligibility for the Program, the New Jersey Division of Taxation determines the value of the available tax benefits (NOLs and R&D Tax Credits), and the New Jersey Commission on Science and Technology evaluates the technology and its viability. The state of New Jersey was the originator of this Program and the first state to implement and fund it.
"As we are always looking for non-dilutive ways to fund our company, we are once again very pleased with NJEDA's decision to support advancing biotechnology companies with the approval of our application in this year's program," stated Christopher J. Schaber, PhD, President and Chief Executive Officer of Soligenix. "This is our seventh year receiving NOL funding and it continues to be a welcomed and important addition to other significant non-dilutive funding we have been awarded from BARDA and NIAID. We are, again, very thankful for New Jersey's continued support of its biotechnology industry."
About Soligenix, Inc.
SGX942 asset phase II data due before end of year. Below is what CEO said about this asset in most recent ER:
Zacks research report: http://s1.q4cdn.com/460208960/files/News/2016/October-7-2016_SNGX_Zeng.pdf?utm_content=buffer613ed&utm_medium=social&utm_source=twitter.com&utm_campaign=buffer
PT: $25 (conservative target)