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Home » Afterthought or proof of efficacy? Adcom to ponder Ipsen post hoc analyses
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Afterthought or proof of efficacy? Adcom to ponder Ipsen post hoc analyses

June 27, 2023
By Mari Serebrov
After nearly 10 years in clinical development and just a few months after an EMA rejection, Ipsen SA will be making its case June 28 before a U.S. FDA advisory committee for its ultra-rare bone disease drug, palovarotene.
BioWorld Regulatory Musculoskeletal U.S. FDA

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