FDA requests more manufacturing data for AbbVie's botox alternative
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AbbVie Provides Update on TrenibotulinumtoxinE (TrenibotE) Biologics License Application in the U.S.
April 23, 2026 4:05 PM EDTU.S. Food and Drug Administration (FDA) issues Complete Response Letter (CRL) for trenibotulinumtoxinE (TrenibotE) related to manufacturing processes; no additional clinical studies are requested As the leader in neurotoxin development and manufacturing, AbbVie is well positioned to address all comments in a timely manner
NORTH CHICAGO, Ill., April 23, 2026 /PRNewswire/ --... More
