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Clinical Trial ● Currently Recruiting Phase I NCT07407933

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

A Study of YL201 in Combination With Other Anti-Cancer Therapies in Patients With Advanced Solid Tumors — Recruiting • Phase I • Oncology • NCT07407933.

📅 10 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase I
NCT ID
NCT07407933
Sponsor
MediLink Therapeutics (Suzhou) Co., Ltd.
Start
2026-03-31
ClinicaliQ Trial Snapshot
  • A Study of YL201 in Combination With Other Anti-Cancer Therapies in Patients With Advanced Solid Tumors — Recruiting • Phase I • Oncology • NCT07407933.
  • What is being tested: YL201 (an investigational cancer therapy) combined with atezolizumab (an immune checkpoint inhibitor) in a phase Ib/II dose escalation and expansion study across multiple centers.
  • Patient eligibility overview: Patients with advanced solid tumors, with Part 1 specifically focusing on previously untreated extensive-stage small cell lung cancer (ES-SCLC) for safety and tolerability assessment.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

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…

Eligibility Snapshot
  • : 1.18 years of age or older. 2. Histologically or cytologically confirmed diagnosis of ES-SCLC 3. Eastern Cooperative Oncology Group performance status of 0 or 1 4. Adequate hematologic and end-organ function

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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