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OncoMatch/Clinical Trials/NCT06825624

ARTEMIS-102: HS-20093 Combinations in Patients with Advanced Metastatic Colorectal Cancer

Is NCT06825624 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments for metastatic colorectal cancer (crc).

Phase 1RecruitingHansoh BioMedical R&D CompanyNCT06825624Data as of May 2026

Treatment: HS-20093 · Bevacizumab · 5-FU · Leucovorin · Capecitabine · OxaliplatinHS-20093 is a fully humanized IgG1 antibody-drug conjugate (ADC) which specifically binds to B7-H3, a target wildly expressed on solid tumor cells. The objectives of this study are to investigate the safety, tolerability, pharmacokinetics and efficacy of HS-20093 in combination with other anti-cancer agents in patients with advanced metastatic colorectal cancer.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: B7-H3 targeted therapy

Previous or current treatment with B7-H3 targeted therapy

Cannot have received: antibody-drug conjugate

Exception: ADCs with topoisomerase I inhibitors as the payload

ADCs with topoisomerase I inhibitors as the payload

Cannot have received: cytotoxic chemotherapy

Any cytotoxic chemotherapy, investigational agents and small molecule targeted therapy within 14 days prior to the first scheduled dose of HS-20093

Cannot have received: small molecule targeted therapy

Any cytotoxic chemotherapy, investigational agents and small molecule targeted therapy within 14 days prior to the first scheduled dose of HS-20093

Cannot have received: macromolecule anti-tumor therapy

Prior treatment with macromolecule anti-tumor therapy or other anticancer drugs within 28 days prior to the first scheduled dose of HS-20093

Cannot have received: other anticancer drugs

Prior treatment with macromolecule anti-tumor therapy or other anticancer drugs within 28 days prior to the first scheduled dose of HS-20093

Cannot have received: radiation therapy

Exception: limited field for palliation within 2 weeks, >30% bone marrow irradiation, or large-scale radiotherapy within 4 weeks prior to first dose

Radiotherapy with a limited field of radiation for palliation within 2 weeks, or patients received more than 30% of the bone marrow irradiation, or large-scale radiotherapy within 4 weeks prior to the first scheduled dose of HS-20093

Cannot have received: major surgery

Major surgery within 4 weeks of the first dose of HS-20093

Lab requirements

Blood counts

Inadequate bone marrow reserve or organ dysfunction [excluded]

Kidney function

Inadequate bone marrow reserve or organ dysfunction [excluded]

Liver function

Inadequate bone marrow reserve or organ dysfunction [excluded]

Cardiac function

Evidence of cardiovascular risk. Severe, uncontrolled or active cardiovascular diseases.

Inadequate bone marrow reserve or organ dysfunction. Evidence of cardiovascular risk. Severe, uncontrolled or active cardiovascular diseases.

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

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