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.
A Study of YL201 in Combination With Other Anti-Cancer Therapies in Patients With Advanced Solid Tumors
At a glance
Conditions
Where it's being run
22 sites across 10 statesWho to contact
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What this trial measures
- 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