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OncoMatch/Clinical Trials/NCT06621563

Phase Ib Trial of HS-20117 in Combination With Other Drugs in Advanced Solid Tumors

Is NCT06621563 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments for solid tumors.

Phase 1RecruitingHansoh BioMedical R&D CompanyNCT06621563Data as of May 2026

Treatment: HS-20117 combined HS-20093 · HS-20117 combined Platinum-containing chemotherapy · HS-20117 combined HS-20093 and 5-FU · HS-20117+CAPEOX · HS-20117+FOLFIRI · HS-20117+mFOLFOX6HS-20117 is a fully-human EGFR-MET immunoglobulin G1(IgG1)-like bispecific antibody. The purpose of study is to evaluate the safety, tolerability, efficacy, PK profile and immunogenicity of HS-20117 in combination with other drugs in advanced solid tumors.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Non-Small Cell Lung Carcinoma

Colorectal Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: MET inhibitor

Any anticancer therapy targeting MET, including TKIs, antibodies or antibody-drug conjugates.

Cannot have received: EGFR-targeted monoclonal or bispecific antibody

Monoclonal or bispecific antibodies targeting EGFR.

Cannot have received: systemic anti-cancer treatment

Systemic anti-cancer treatment (Cytotoxicities and anti-cancer Traditional Chinese medicine or TKIs) within 2 weeks prior to the first dose of HS-20117.

Cannot have received: investigational anti-cancer drugs or antibodies or ADCs

Investigational anti-cancer drugs or antibodies or ADCs within 4 weeks prior to the first dose of HS-20117.

Cannot have received: local radiotherapy

Local radiotherapy within 2 weeks prior to the first dose of HS-20117, more than 30% of bone marrow irradiation or large-area radiotherapy within 4 weeks before the first dose of HS-20117.

Cannot have received: major surgery

Major surgery within 4 weeks prior to the first dose of HS-20117.

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

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