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GSK Secures Ex-China Rights to 12 Hengrui Drug Programmes in $12.5 Billion Deal

GSK secured a $500 million upfront payment to develop PDE3/4 inhibitor HRS-9821, plus 11 preclinical candidates, under a milestone-based collaboration that has Hengrui leading Phase I trials

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Signage is pictured in the main lobby of GSK offices in London, Britain, February 20, 2025. REUTERS/Chris J. Ratcliffe/File Photo
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Overview

  • GSK will pay $500 million upfront and could disburse up to $12 billion more upon achievement of development, regulatory approval and sales milestones
  • The agreement grants GSK exclusive development and commercialization rights outside mainland China, Taiwan, Hong Kong and Macau for HRS-9821 and 11 additional Hengrui programmes
  • HRS-9821 is a PDE3/4 inhibitor in Phase I testing for COPD that has demonstrated bronchodilation and anti-inflammatory effects and may be delivered via dry-powder inhaler
  • The collaboration covers up to 12 candidates across respiratory, oncology, immunology and inflammation, with Hengrui responsible for Phase I development and GSK holding global commercialization options thereafter
  • The deal highlights China’s growing R&D influence as pharmaceutical out-licensing values approached $66 billion in the first half of 2025, boosting multinational pipeline diversification