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

This study is testing a new combination of two anti-cancer drugs, YL201 and atezolizumab, for people with advanced solid tumors, specifically extensive-stage small cell lung cancer (ES-SCLC). The main goal is to see how safe and tolerable this combination is, especially looking at any dose-limiting toxicities (side effects that are too severe). Researchers will also track other side effects over a longer period. You might be able to join if you are 18 or older, have ES-SCLC that hasn't been treated with systemic anti-cancer therapy before, and meet certain health requirements. The study is looking for about 118 participants.

Study design
This is a Phase Ib/II, multicenter, open-label study. It involves two parts: a dose escalation to find the safest dose, followed by dose optimization and expansion stages. Participants will be randomized in one part of the study.
What's involved
YL201 and atezolizumab will be given intravenously (into a vein) on Day 1 of each 21-day cycle. The study treatment continues until disease progression or death.
Compensation
Not stated in the trial record.
Follow-up
Adverse events will be monitored from the first dose of study treatment up to disease progression or death from any cause, for up to approximately 6 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07407933

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

Recruiting
PHASE1Ages 18+InterventionalTreatment
MediLink Therapeutics (Suzhou) Co., Ltd.
~118 participants
Updated 2026-06-15 on ClinicalTrials.gov
What's tested:YL201Atezolizumab

At a glance

Recruiting sites
21 of 22 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Nature and Frequency with Dose-Limiting Toxicities (DLTs)
Measured over 21 days
+1 more outcome measured
Thoracic Neoplasms, Lung Diseases, Small Cell Lung Carcinoma
22 sites across 10 states
Spain10
Poland3
Italy2
District of Columbia1
Kentucky1
Texas1
Virginia1
Belgium1

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  • Nature and Frequency with Dose-Limiting Toxicities (DLTs)21 days
  • Adverse EventsFirst dose of study treatment up to disease progression or death from any cause (up to approximately 6 years)

    Incidence, nature, and severity of AEs graded according to the NCI CTCAE v5