OncoMatch

OncoMatch/Clinical Trials/NCT06107686

A Study of YL202 in Selected Patients With Advanced Solid Tumors

Is NCT06107686 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies YL202 should be intravenously infused for nsclc.

Phase 2RecruitingMediLink Therapeutics (Suzhou) Co., Ltd.NCT06107686Data as of Jun 2026Location: China

Treatment: YL202 should be intravenously infusedThis study is a multicenter, open-label, phase II study of YL202 in China to evaluate the efficacy, safety, and PK characteristics of YL202 in the following selected patients with advanced solid tumors.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Other

YL202 should be intravenously infused

Cancer type

Non-Small Cell Lung Carcinoma

Breast Carcinoma

Head and Neck Squamous Cell Carcinoma

Tumor Agnostic

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: HER3-targeted therapy

prior drug therapy targeting HER3 (including antibodies, antibody-drug conjugates [ADCs])

Cannot have received: CAR-T cell therapy

chimeric antigen receptor T-cell immunotherapy (CAR-T)

Cannot have received: topoisomerase I inhibitor

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

Cannot have received: antibody-drug conjugate

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 before the first dose.

Kidney function

The function of organs and bone marrow meets the requirements within 7 days before the first dose.

Liver function

The function of organs and bone marrow meets the requirements within 7 days before the first dose.

The function of organs and bone marrow meets the requirements within 7 days before the first dose.

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

Frequently asked questions

Is NCT06107686 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior HER3-targeted therapy, CAR-T cell therapy, topoisomerase I inhibitor disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify