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Fennec Pharmaceuticals Ord Shs T.FRX

Alternate Symbol(s):  FENC

Fennec Pharmaceuticals Inc. is a commercial-stage biopharmaceutical company focused on its product candidate PEDMARK. It sells its product through a field force, including Regional Pediatric Oncology Specialists and medical science liaisons who are helping to educate the medical communities and patients about cisplatin induced ototoxicity and its programs supporting patient access to PEDMARK. PEDMARK is a Food and Drug Administration approved therapy indicated to reduce the risk of ototoxicity associated with cisplatin treatment in pediatric patients with localized, non-metastatic, solid tumors. It is a formulation of sodium thiosulfate in single-dose, ready-to-use vials for intravenous use in pediatric patients. PEDMARK is a therapeutic agent with a dosing paradigm, across two open-label, randomized Phase 3 clinical studies, the Clinical Oncology Group (COG) Protocol ACCL0431 and SIOPEL 6. It has established Fennec HEARS, a single source program designed to connect PEDMARK patients.


TSX:FRX - Post by User

Post by commissionson Nov 09, 2004 10:43am
199 Views
Post# 8155116

News Release

News ReleaseDid some digging regarding what was in the news release and its significance.In the last 20 or so years no drug has recieved FDA approval - that did not show an objective partial response in its phase 1 human trials. Essentially if this was not shown your chances were the equivalent of 1 in 1000. However of the drugs that did get an objective partial response their approval chances increased to approx. 1 in 10. I wonder how many people selling are aware of this relationship. This data is very good in that we are now looking at 3 ways that Exherin can be effective, 1. as a cocktail with chemo 2. as a VTA that destroys the cells surrounding the tumour by cutting off the blood supply and effectively starving the tumour and 3. which is the gem of the phase one trials - it is attacking the coreof the tumour itself Although there have been critics as to how long this trial has taken the findings will be absolutely essential in stream lining the US and European trials that will not only save alot of precious $$'s -but also quicken the route to phase 3's and ultimately commercialization because if it. Commissions They now know to only target N-cadherin positive, they know how to release the dosage to eliminate side affects, and they now know that that Exherin is capable of affecting the tumour itself.
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