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A phase 3 trial testing YL202 in non-small-cell lung cancer, now recruiting.
Pivotal Study to Evaluate YL202 Versus Docetaxel in Patients With Locally Advanced or Metastatic EGFR Sensitive Mutation Non-Squamous Non-Small Cell Lung Cancer is a phase 3 interventional study registered as NCT07416994, led by MediLink Therapeutics (Suzhou), and recruiting on the registry. Official title: A Multicenter, Randomised, Open-label, Phase III Study to Compare the Efficacy and Safety of YL202 and Docetaxel in Patients With Locally Advanced or Metastatic EGFR Sensitive Mutation Non-Squamous Non-Small Cell Lung Cancer. Planned enrolment is 440 participants (estimated). The study started in 2026-03-18 and primary completion is expected in 2028-08-31. No results have been posted on ClinicalTrials.gov.
The full inclusion and exclusion criteria are on the registry record. Read 2026-10-07. Recruiting overall does not mean a particular site is open; ask the study team.
ClinicalTrials.gov data courtesy of the US National Library of Medicine.
Shares YL202, MediLink Therapeutics, Non-small-cell lung cancer.
Shares YL202, MediLink Therapeutics.
Shares YL202, MediLink Therapeutics, Non-small-cell lung cancer.
Shares YL202, MediLink Therapeutics, Non-small-cell lung cancer.
Shares YL202, MediLink Therapeutics.
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