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MotionMan

02/24/12 2:29 PM

#137798 RE: DewDiligence #137796

VVUS- You believe that they get thumbs up at the Cardiac panel and final FDA approval?
I'm surprised to see so many analysts negative on approval still with the 20-2 vote and the positive panel discussion.

Anyone care to give a probability that VVUS gets the Dendreon treatment from the FDA?
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hptaxis

02/24/12 2:38 PM

#137800 RE: DewDiligence #137796

Isn't that still a large number - in the millions?
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olddogwithnewtrix

02/24/12 2:58 PM

#137807 RE: DewDiligence #137796

Sorry, my response was not the same topic. For Qnexa, I will say 500-600 million the 1st year. all depends on the right partner/buyer and marketing.
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pcrutch

02/24/12 3:18 PM

#137808 RE: DewDiligence #137796

Couldn't the existence of Qnexa and lack of sufficient trial data using the generic components could open them up to medical malpractice? Figure some docs might be more cautious about subscribing the two generics separately than just using Qnexa
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biomaven0

02/24/12 10:44 PM

#137841 RE: DewDiligence #137796

Qnexa will have less than a 40% Rx share of the combined market for Qnexa and the off-label generic constituents



Not sure what the number will be as it depends on the REMS and on pricing/insurance coverage, but I would predict distinctly north of 50% - if I had to pick a number, I'd pick mid 60's.

Peter
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ciotera

02/25/12 10:10 AM

#137853 RE: DewDiligence #137796

Qnexa will have less than a 40% Rx share



Are you including all uses of topiramate here?