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OncoMatch/Clinical Trials/NCT07208773

A Study of YL201 and Ivonescimab (AK112) in Advanced Solid Tumors

Is NCT07208773 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including YL201 and Ivonescimab for advanced solid tumors.

Phase 1/2RecruitingMediLink Therapeutics (Suzhou) Co., Ltd.NCT07208773Data as of May 2026

Treatment: YL201 · IvonescimabThis study was designed to evaluate the efficacy and safety of YL201 in combination with Ivonescimab (AK112) in subjects with solid tumor.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Small Cell Lung Cancer

Biomarker criteria

Required: EGFR mutation

Disease stage

Required: Stage IV

Metastatic disease required

Phase 1: Advanced Solid tumors. Phase 2: Extensive-stage SCLC, Non-AGA NSCLC, EGFR mutation NSCLC.

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: B7-H3-targeted therapy

previous treatment with drugs targeting B7-H3 (including antibodies, ADCs, CAR-T, and other drugs)

Cannot have received: topoisomerase I inhibitor

previous treatment with topoisomerase I inhibitors or ADCs containing topoisomerase I inhibitors

Lab requirements

Blood counts

functions of body organs and bone marrow meet the requirements

Kidney function

functions of body organs and bone marrow meet the requirements

Liver function

functions of body organs and bone marrow meet the requirements

Within 7 days before the first dose, the functions of body organs and bone marrow meet the requirements.

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

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