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Kelun-Biotech says Phase 3 sac-TMT plus Keytruda meets PFS endpoint in first-line PD-L1-negative NSCLC
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Kelun-Biotech says Phase 3 sac-TMT plus Keytruda meets PFS endpoint in first-line PD-L1-negative NSCLC
  • Sichuan Kelun-Biotech reported its Phase 3 OptiTROP-Lung06 study met the primary endpoint of progression-free survival at interim analysis.
  • Trial tested TROP2 ADC sacituzumab tirumotecan (sac-TMT) with Merck’s Keytruda versus chemotherapy with Keytruda in first-line PD-L1-negative non-squamous NSCLC.
  • Combination showed a statistically significant, clinically meaningful PFS improvement; overall survival trended positive.
  • Safety profile matched prior studies; no new safety signals flagged.
  • Company plans talks with China’s NMPA drug review center on a potential regulatory pathway based on the results.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. published the original content used to generate this news brief via IIS, the regulatory disclosure system operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260715-12244468), on July 14, 2026, and is solely responsible for the information contained therein.

Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
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