RecruitingPhase 2NCT07202364

A Study of YL202 in Patients With Advanced Solid Tumors

A Multicenter, Open-Label, Phase II Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of YL202 in Selected Patients With Advanced Solid Tumors


Sponsor

MediLink Therapeutics (Suzhou) Co., Ltd.

Enrollment

100 participants

Start Date

Aug 4, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a multicenter, open-label, phase II study of YL202 in China to evaluate the efficacy, safety, and PK characteristics of YL202 in selected patients with advanced solid tumors.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called YL202 in people with advanced solid tumors — including certain types of lung cancer, colorectal cancer, cervical cancer, or other cancers that have spread. The drug is a type of targeted therapy designed to attack cancer cells. **You may be eligible if...** - You are 18 or older with a BMI between 18 and 32 - You have been diagnosed with advanced non-squamous lung cancer, colorectal cancer, cervical cancer, or another advanced solid tumor - You have already received 1 or 2 rounds of treatment for your advanced cancer - You have at least one measurable tumor outside the brain - You have tumor tissue available for testing - Your overall health and ability to function is rated as good (ECOG 0 or 1) - You are expected to live at least 3 more months **You may NOT be eligible if...** - You have previously been treated with a drug that targets HER3 - You could not tolerate a type of chemotherapy called topoisomerase I inhibitors before - You have untreated brain metastases or cancer in the lining of the brain - You have uncontrolled heart, lung, or liver problems - You have active hepatitis B, hepatitis C, or HIV - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGYL202

YL202 will be intravenously infused over 60±10 min


Locations(1)

Hunan Provincial Tumor Hospital

Changsha, Hunan, China

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NCT07202364


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