A Study of YL201 in Combination With Other Anti-Cancer Therapies in Patients With Advanced Solid Tumors

This is a phase Ib/II, multicenter, open-label study of YL201 combined with atezolizumab. The study will include 2 parts. Part 1 of the study is a dose escalation in participants with previously untreated ES-SCLC to determine the safety and tolerability of YL201 in combination with fixed dose of atezolizumab. The planned dose levels of YL201 are 1.2 mg/kg, 1.6 mg/kg and 2.0 mg/kg. Part 2 consists of a dose optimization stage followed by a dose expansion stage. During the dose optimization stage, participants will be randomized 1:1:1 to receive either YL201 at 1.2 mg/kg,1.6 mg/kg or 2.0 mg/kg Q

Trial Details

NCT ID
NCT07407933
Phase
PHASE1 / PHASE2
Sponsor
MediLink Therapeutics (Suzhou) Co., Ltd.
Status
RECRUITING
Cancer Type
Lung Cancer
Interventions
  • YL201
  • Atezolizumab
Locations (sample)
  • Washington D.C., District of Columbia, United States|38.89511,-77.03637
  • Louisville, Kentucky, United States|38.25424,-85.75941
  • Houston, Texas, United States|29.76328,-95.36327
  • Fairfax, Virginia, United States|38.84622,-77.30637
  • Namur, Belgium|50.4669,4.86746

Key Eligibility Criteria

  • 18 years of age or older. 2. Histologically or cytologically confirmed diagnosis of ES-SCLC 3. Eastern Cooperative Oncology Group performance statu…

For full eligibility, visit ClinicalTrials.gov.

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