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CANbridge’ CAN108 (Livmarli) Receives TFDA Approval for the Treatment of Cholestatic Pruritus in Patients with Alagille Syndrome in Taiwan

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CANbridge’ CAN108 (Livmarli) Receives TFDA Approval for the Treatment of Cholestatic Pruritus in Patients with Alagille Syndrome in Taiwan

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  • TFDA has approved CAN108 (Livmarli), a minimally absorbed ileal bile acid transporter inhibitor for cholestatic pruritus in patients with ALGS aged ≥1yr. The approval was based on the (ICONIC) study & (RISE) infant safety study as well as data from the program in patients with ALGS
  • The (ICONIC) study showed a significant & clinical reduction in pruritus over PBO and reductions in serum bile acids which were durably maintained over several years of treatment. Interim data from the (RISE) study supports the indication in the infant group at the age of ≤12mos.
  • Livmarli is being studied in late-stage clinical studies in other rare cholestatic liver diseases. The therapy received BTD for ALGS & PFIC type 2; ODD for ALGS, PFIC, and BA from the US FDA

Ref: PR Newswire | Image: Canbridge

Related News:- Mirum’s Livmarli Receives Health Canada Authorization for Cholestatic Pruritus in Patients with Alagille Syndrome

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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