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Purpose Pharma’s Attrogy Secures the EC’s Approval for the Treatment of Hereditary Transthyretin-mediated Amyloidosis   

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  • The EC has approved Attrogy (diflunisal) to treat hereditary transthyretin-mediated amyloidosis (hATTR amyloidosis) in adults with stage 1 or 2 polyneuropathy in all EEA states  
  • EC approval was based on a P-III trial showing that diflunisal significantly slowed disease progression in patients with TTR amyloidosis. At 24 mos. baseline, 1EP met diflunisal led to a mean NIS+7 increase of 8.2 points vs. 26.3 with PBO. 2EPs, including NIS, NIS-LL, Kumamoto score, and SF-36 physical score, also showed significant benefits vs PBO  
  • Diflunisal (250 mg BID), a difluorophenyl salicylic acid derivative, stabilizes the TTR tetramer 

Ref: Purpose Pharma | Image: Purpose Pharma| Press Release

Related News:- Purpose Pharma’s Attrogy Receives the CHMP’s Positive Opinion for the Treatment of Hereditary Transthyretin-mediated Amyloidosis  

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