SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Regeneron Pharmaceuticals -- Ignore unavailable to you. Want to Upgrade?


To: Biotech Jim who wrote (1674)10/29/2014 2:24:51 PM
From: Miljenko Zuanic  Read Replies (1) | Respond to of 3559
 
Yesterday announcement of the increase in pts enrolment number in outcome trials suggest (regardless what any company claim as true reason) that event rate are slower and need more power to detect difference, if any. Improve-it trial definitely does not look good, as positive outcome for Zetia is "distant future", IMO.
AMGN atheroma trial is very interesting, and after yesterday presentation wish that AMGN is regn-partnet, not Sanofi. Anyway, will se how DESPERATE is Sanofi to BURST grow in next 1-2 years (or even longer near term interval). REGN Eyela would fit nicely, but CULTURE is so DIFERENT!
Quote: "Asked for the umpteenth time earlier this year why he just doesn't buy Regeneron, Viehbacher bluntly said that "We'd probably screw it up." That's not a big endorsement for in-house R&D. ...Agree 1000%!



To: Biotech Jim who wrote (1674)11/10/2014 11:50:32 AM
From: Miljenko Zuanic  Read Replies (1) | Respond to of 3559
 
This morning we have good news, AMGN-NDA accepted for review by FDA, for the short term “surrogate” indication, without(?) or with “minimal" medical claim. Now, I believe that FDA staff has in advance results from IMPROVE-IT, and that results are: “good trend toward medical benefit”! This leave REGN with chance to file NDA with “partial medical claim”, because by 2015-mid-year they will have advance “post-hock” outcome results from 18(24) months-safety study.

finance.yahoo.com



To: Biotech Jim who wrote (1674)11/17/2014 9:25:45 AM
From: Biotech Jim  Read Replies (2) | Respond to of 3559
 
Monday, November 17, 2014 8:30 am EST

mercknewsroom.com

Merck Announces that IMPROVE-IT Achieved Primary Endpoint; Data to be Presented at American Heart Association Scientific Sessions Today

Data are Embargoed by American Heart Association until 10:45 AM CT Today