Zacks Investment Research | Mar 07, 2018 08:19PM ET
Key highlights of the week include FDA’s acceptance of Regeneron/Sanofi's Dupixent sBLA for asthma, Biogen/AbbVie’s decision to withdraw multiple sclerosis drug, Zinbryta, due to risk of liver failure and Celgene’s completion of Juno acquisition.
Recap of the Week’s Most Important Stories
Regeneron/Sanofi's Dupixent sBLA for Asthma Accepted by FDA: Regeneron (NASDAQ:REGN) and partner Sanofi (PA:SASY) (SNY) announced that the FDA has accepted for review the supplemental Biologics License Application (sBLA) of Dupixent (dupilumab) as an add-on maintenance treatment in adults and adolescents (12 years of age or older) with moderate-to-severe asthma. The FDA has set a target action date of Oct 20, 2018 per the Prescription Drug User Fee Act. The sBLA was supported by results from the three pivotal trials from the LIBERTY ASTHMA clinical development program. Sanofi and Regeneron are studying dupilumab in a broad range of clinical development programs for diseases driven by Type 2 inflammation, including pediatric atopic dermatitis (phase III), nasal polyps (phase III) and eosinophilic esophagitis (phase III).
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What's Next in the Biotech World?
Stay tuned for more regulatory and pipeline updates.
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