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Morning Briefing

Summaries of health policy coverage from major news organizations

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Wednesday, Apr 13 2016

Full Issue

FDA Panel Shoots Down Early Approval Request For Experimental Lung-Cancer Treatment

The advisory panel is recommending that the Food and Drug Administration wait for data from a phase 3 clinical trial before deciding on Clovis' rociletinib. In other agency news, an FDA official says long-awaited biotech medicine guidelines are still in the works.

The Wall Street Journal: FDA Panel Opposes Approval Of Clovis Lung-Cancer Treatment

Clovis Oncology Inc. said a U.S. Food and Drug Administration advisory panel voted to recommend against early approval for the biopharmaceutical company’s experimental lung-cancer treatment. Shares fell 5.4% on Tuesday during the regular session and declined a further 3% to $13.81 in recent after-hours trading. It is the latest setback for Clovis whose lung-cancer treatment—called rociletinib—faces competition from a rival drug from AstraZeneca PLC called Tagrisso, which received U.S. regulatory approval earlier in November. (Stynes, 4/12)

CQ Healthbeat: FDA Still Working On Guidelines For Copycat Biotech Drugs

The director in charge of FDA’s biotechnology products office said Tuesday the agency continues to work on a long-awaited guidance to inform manufacturers of copycat biotech medicines how to prove similarity to the brand-name drug. (Williams, 4/12)

This is part of the Morning Briefing, a summary of health policy coverage from major news organizations. Sign up for an email subscription.
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