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A phase 2 trial of YL202 should be intravenously infused in advanced solid tumours, run by MediLink Therapeutics (Suzhou) Co., Ltd., now recruiting.
A Phase 2 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of YL202 in Patients With BC is a phase 2 interventional study registered as NCT06439771 by MediLink Therapeutics (Suzhou) Co., Ltd., with 180 participants planned, started 2024-04-23 and due to reach its primary completion in 2026-07-30. Interventions recorded: YL202 should be intravenously infused.
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