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).
Treatment: HS-20093 · Bevacizumab · 5-FU · Leucovorin · Capecitabine · Oxaliplatin — HS-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.
Check if I qualifyExtracted 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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