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OncoMatch/Clinical Trials/NCT07202364

A Study of YL202 in Patients With Advanced Solid Tumors

Is NCT07202364 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies YL202 for non small cell lung cancer.

Phase 2RecruitingMediLink Therapeutics (Suzhou) Co., Ltd.NCT07202364Data as of May 2026

Treatment: YL202This 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.

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Extracted eligibility criteria

Cancer type

Small Cell Lung Cancer

Colorectal Cancer

Cervical Cancer

Tumor Agnostic

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 2 prior lines
Min 1 prior line

Cannot have received: HER3-targeted therapy

Prior drug therapy targeting HER3

Cannot have received: topoisomerase I inhibitor

Previously intolerant to topoisomerase I inhibitors or ADC therapy composed of topoisomerase I inhibitors

Cannot have received: allogeneic bone marrow transplantation

Prior treatment with allogeneic bone marrow transplantation

Cannot have received: solid organ transplantation

Prior treatment with ... solid organ transplantation

Lab requirements

Blood counts

The function of organs and bone marrow meets the requirements within 7 days prior to the first dose

Kidney function

The function of organs and bone marrow meets the requirements within 7 days prior to the first dose

Liver function

The function of organs and bone marrow meets the requirements within 7 days prior to the first dose

The function of organs and bone marrow meets the requirements within 7 days prior to the first dose

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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