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September 8, 2007

Encysive, the FDA and the Dispute Resolution Process

by @ 3:58 pm.  Filed under Pharma News

Forbes recently had an article on fighting the FDA.

You Can’t Fight The FDA - Forbes.com

I have been watching this drama play out for sometime now and for me it is like watching a train wreck. You know what’s going to happen, you know it isn’t going to be pretty but there’s nothing you can do to stop it from happening. I’m not sure I understand Encysive’s rational for going through this dispute resolution process as it seemed doomed from the start.

Eye on FDA mentioned this in the Weekly Roundup - 9-7-07 and had a great article on this situation earlier: Eye on FDA: What’s at Stake with Formal Dispute Resolution

Other recent articles on this.

Encysive Pharmaceuticals Investor Relations
FDA: Encysive Drug Not Effective Enough - Forbes.com
PharmaLive: Encysive Pharmaceuticals Receives Written Response From FDA On Its Request for Formal Dispute Resolution for Thelin (Sitaxsentan Sodium)

Other Sources

fda encysive - Yahoo! Search Results
fda encysive - Google Search
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Clusty Search » fda encysive

Clusty Blogs » fda encysive
fda encysive - Google Blog Search

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Email Ed Vawter



Related Posts:
  • Encysive To Evaluate Options
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    September 7, 2007

    No Generic biologics in FDA legislation

    by @ 2:36 pm.  Filed under FDA, Pharma News, Pharma

    Reuters is reporting that the new FDA legislation is unlikely to have any biogenerics in it.

    UPDATE 1-Lawmakers: Generic biologics unlikely in FDA bill | Health | Reuters

    I personally think there should be something at least giving a timeframe on when the FDA should have to present a report to Congress on how and when they will implement some kind of program.

    Here is the key from my perspective.

    The chances of adding the generic biologics measure to a broad FDA bill now moving through Congress are “extremely slim,” Rep. Henry Waxman, a California Democrat, told a Generic Pharmaceutical Association conference.

    I realize that biologics are not like standard drugs in terms of generics but really think that until Congress demands that the FDA come up with some sort of plan, nothing will move forward. It is too bad that Europe will be the one taking the forefront in this movement. As an example, EMEA just approved a follow-on for EPO for Sandoz, Novartis’ generics division.

    Sandoz Receives European Commission Approval for biosimilar epoetin alfa

    I know there will be a lot of lobbying of Congress on this issue but think that regardless there needs to be some sort of plan put forward. Just trying to delay and avoid the issue is only going to cause more public relations problems for biotech in the future.

    Other Recent Stories Related to Biogenerics

    Biotech firms will soon lose patent protection - Sep. 5, 2007
    Lawmakers Offer U.S. Plan for Generic Biotech Drugs
    RED HERRING | Going Generic
    Follow-on biologics ‘not substitutable’, says BIO
    Biopharmaceuticals | Follow-on Biologics: Friend or Foe? | Pharmaceutical Manufacturing
    Patent Baristas » Senate Committee Approves Follow-On Biologics Bill: Fear and Trepidation Follow
    Biologics Price Competition and Innovation Act of 2007 (S. 1695)

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    Related Posts:
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  • The FDA and Biogenerics

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    More on Mergers

    by @ 2:36 pm.  Filed under Pharma News

    I’m not going to comment on these other than to say the merger mania continues. Here are some recent headlines.

    PharmaLive: Shareholders Approve Peptech-EvoGenix Merger :
    PharmaLive: Ametek Acquires Cameca SAS
    PharmaLive: GeoPharma Announces Shareholder Approval of Merger with Dynamic Health Products
    Meda AB to Buy MedPointe Pharmaceuticals for $800 Million in Cash, Stock - News, Search Jobs, Events

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