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Oncolytics Biotech Inc T.ONC

Alternate Symbol(s):  ONCY

Oncolytics Biotech Inc. is a clinical-stage biotechnology company. The Company is focused on developing pelareorep, an intravenously delivered immunotherapeutic agent that activates the innate and adaptive immune systems and weakens tumor defense mechanisms. This compound induces anti-cancer immune responses and promotes an inflamed tumor phenotype turning cold tumors hot through innate and adaptive immune responses to treat a variety of cancers. This improves the ability of the immune system to fight cancer, making tumors more susceptible to a broad range of oncology treatments. The Company’s primary focus is to advance its programs in hormone receptor-positive / human epidermal growth factor 2- negative (HR+/HER2-) metastatic breast cancer and advanced/metastatic pancreatic ductal adenocarcinoma to registration-enabling clinical studies. In addition, it is exploring opportunities for registrational programs in other gastrointestinal cancers through its GOBLET platform study.


TSX:ONC - Post by User

Bullboard Posts
Comment by bilosellhion Jun 01, 2003 10:51pm
262 Views
Post# 6134248

RE: Equity Position

RE: Equity Positionbjork 30% royalties are a fantasy... the mystery isn't really that difficult to figure out, but let me try to help you and make it really simple for you to understand - 10% of potentially billions in annual revenues will make you well-off as will 25% of the same amount. apparently you prefer to increase the risk of failure, perhaps significantly, to have a chance at being filthy rich. the only thing onc should be worrying about now is that which will determine if they can attract a reputable partner. that means ensuring they have adequate resources to complete their ph II trials in a timely manner and ensuring that those trial results are sufficiently large that they are statistically valid and reliable to withstand the scrutiny of a potential partner. if you had read my post in context, you may have figured out (assuming you are capable) that if they screw up with the trials eg. insufficient enrollees or trial size, design protocols that have inadequate measures of safety & efficacy, one vs. multiple injections, etc., the resulting delays and/or insufficient results will add to the need for additional ph III testing which will cost them time, money and optimal partnership terms. per the kudlow interview with the new FDA chairman, new drug development costs to the end of ph III typically amount to approx $900M US - for a partner to spend that kind of money on reolysin and essentially still assume all the risks (which will still be significant in ph III - see erbitux) for 50-70% of the potential sales, is dreaming, imo. then again, even a 10% royalty may be a fantasy. thats all the fun and games for tonite. you can now return to LA-LA land.
Bullboard Posts