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Pharma Roundup: Lilly and Prasugrel, Roche and Genentech, and More

By John Maas | Jan 30, 2009

Prasugrel’s FDA approval looks closer — Prasugrel, the blood thinner on which Lilly is pinning so much hope, got a boost in a newly-published FDA document stating that “the Division recommends approval of prasugrel.” The briefing is meant to sway the outside committee that will convene next week to advise the FDA on the drug. [Source: WSJ Health Blog]

Roche lowers Genentech bid, but Genentech might be worth more in springGenentech is not pleased by Roche’s reduced buyout offer; BNET’s Jim Edwards has the story. Meanwhile, some analysts say Roche’s move is foolish, since many expect Genentech to announce good experimental results on cancer drug Avastin, results which could raise the company’s worth. [Source: Pharma's Market]

Deerfield buys NitroMed — A smallish saga on the biotech front has ended, with NitroMed rejecting Archemix (whose buyout looked like a done deal before Deerfield walked onto the scene) for Deerfield Management, the company which already owns 12%. [Source: FierceBiotech]

U.K. flu deal for Glaxo and RocheGSK will provide 10.6 million doses of flu treatment to the government of the United Kingdom; Roche will provide 7.6 million. The deal will give the U.K. a drug stockpile to treat half of its population. The financial terms of the contract have not been disclosed. [Source: Reuters, via Corey Nahman]

BNET User Analysis

Web Buzz:
  • Odds Improve for Lilly’s Prasugrel-ImClone Gamble

    BNET Insight - 339 days 12 hours 49 minutes ago

    A panel of the European Medicines Agency recommended the approval of prasugrel, Eli Lilly’s new blood thinner, and such recommendations are usually followed by the agency within a couple of months, Reuters reports. The news is a significant win in Lilly’s long campaign to get this drug to market. It also means that Lilly CEO John...

  • FDA committee backs Lilly's prasugrel

    Fierce Pharma - 297 days 9 hours 25 minutes ago

    After months of delays, Eli Lilly and Daiichi Sankyo finally have word on the status of their anti-clotting drug prasugrel. An FDA advisory committee released a hefty briefing on prasugrel, ahead of a meeting of cardiology experts scheduled for next week. Buried deep in that report is the one sentence that likely comes as music to Lilly...

  • Analysts Rain on Lilly's Effient Parade; 70% of Sales Go Generic After 2011

    BNET Pharma - 133 days 13 hours 7 minutes ago

    The FDA’s approval of Eli Lilly’s new blood-thinner, Effient/prasugrel, was a huge moment for a company that has not had a new drug approved in five years. But Wall Street’s analysts seem determined to rain on Lilly’s parade. The spreadsheet jockeys grumbled Friday evening about the black box warning and the assumed price premium over...

  • NICE gives limited blessing to Effient

    Fierce Pharma - 80 days 13 hours 18 minutes ago

    Eli Lilly's new blood thinner Effient got the nod from the U.K.'s National Institute for Health and Clinical Excellence. Good, right? Yes, to a point. The cost-effectiveness gatekeeper decides whether the National Health Service will pay for specific treatments, and its approval often sways other governments' buying decisions. But NICE gave...

  • EMEA panel backs Lilly's prasugrel

    Fierce Pharma - 339 days 14 hours 2 minutes ago

    Good news for Eli Lilly. While Lilly was holding its breath for a response from the FDA for its experimental drug, prasugrel, the company managed to gain an endorsement from an EMEA advisory panel. The committee's recommendation will go to the European Commission, which usually makes a decision in two to three months, according...

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