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LianBio Reports the NMPA Acceptance of NDA and Granted Priority Review of Mavacamten for Obstructive Hypertrophic Cardiomyopathy

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LianBio Reports the NMPA Acceptance of NDA and Granted Priority Review of Mavacamten for Obstructive Hypertrophic Cardiomyopathy

Shots:

  • The NDA was based on the P-III trial (EXPLORER-HCM) evaluating mavacamten vs PBO in 251 patients
  • The trial met its 1EPs & 2EPs and also showed a robust treatment effect with clinical improvements in exercise capacity, functional status & PROs as well as the ability to relieve left ventricular outflow tract obstruction
  • The NDA also contains clinical results from a P-I PK study of mavacamten in healthy Chinese volunteers which demonstrated a safety & tolerability profile, as well as a PK profile similar to P-I PK studies, carried out in the US. Blinded preliminary safety data from an ongoing P-III trial (EXPLORER-CN) of mavacamten also supported the early NDA filing & the results are anticipated in mid-2023

Ref: LianBio | Image: LianBio

Related News:- BMS’ Camzyos (mavacamten) Receives the US FDA’s Approval for the Treatment of Symptomatic New York Heart Association Class II-III Obstructive HCM

Click here to­ read the full press release 

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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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