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FDA approves Ipsen s Iqirvo to address unmet need in primary biliary cholangitis

The FDA granted accelerated approval to Ipsen Pharma’s Iqirvo 80 mg, a first-in-class oral, once-daily peroxisome proliferator-activated receptor agonist for the treatment of primary biliary cholangitis, according to a company release. Originally given breakthrough therapy designation in 2019, Iqirvo (elafibranor, Ipsen/Genfit), is now indicated as second-line therapy in combination with

FDA Grants Accelerated Approval to Elafibranor (Iqirvo) for PBC

Newswire & Press Release / Ipsen s Iqirvo® Receives U S FDA Accelerated Approval as A First-in-class PPAR Treatment for Primary Biliary - Pharma / BioTech / Nutrition - IPSEN Group

Newswire & Press Release / Ipsen s Iqirvo® Receives U S FDA Accelerated Approval as A First-in-class PPAR Treatment for Primary Biliary - Pharma / BioTech / Nutrition - IPSEN Group
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Newswire & Press Release / Ipsen s Iqirvo® Receives U S FDA Accelerated Approval as A First-in-class PPAR Treatment for Primary Biliary - Pharma / BioTech / Nutrition - IPSEN Group

Newswire & Press Release / Ipsen s Iqirvo® Receives U S FDA Accelerated Approval as A First-in-class PPAR Treatment for Primary Biliary - Pharma / BioTech / Nutrition - IPSEN Group
newswiretoday.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from newswiretoday.com Daily Mail and Mail on Sunday newspapers.

Ipsen, Genfit Drug That Missed in MASH Wins FDA Approval in a Much Rarer Liver Disease

Ipsen, Genfit Drug That Missed in MASH Wins FDA Approval in a Much Rarer Liver Disease
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