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Hepatic arterial infusion versus intravenous oxaliplatin in a safety, feasibility, and pharmacokinetic study of liver-dominant malignancies – ARTEMIS OXYS-I trial

Status
Not yet recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2026-527509-39-01
Enrollment
13
Registered
2026-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal liver metastases, Intrahepatic cholangiocarcinoma

Brief summary

• The (dose-corrected) difference in intra-tumoral total platinum concentrations following administration of HAI oxaliplatin versus IV oxaliplatin

Detailed description

• Difference in intra-tumoral total platinum concentration following HAI 130 mg/m² versus HAI 85 mg/m²., • Difference in non-tumorous liver tissue total platinum concentration following IV 85 mg/m² versus HAI 85 mg/m²., • Difference in non-tumorous liver tissue total platinum concentration following HAI 130 mg/m² versus HAI 85 mg/m²., • Systemic pharmacokinetic parameters of total platinum, including plasma levels, Cmax, Tmax, Area Under the Curve (AUC), t1/2, Cl, Vd after administration of oxaliplatin via intravenous infusion versus via hepatic arterial infusion., • Incidence and grade of adverse events per treatment cycle and cumulative over the entire treatment period according to NCI CTCAE v6.0, • Post-procedural complications according to the modified CIRSE classification., • Feasibility parameters including completion rate of all planned oxaliplatin administrations and liver biopsies, technical success of HAI procedures, adherence to scheduled blood sampling, need for dose modifications or treatment delays due to safety or technical issues, and patient-reported tolerability of study procedures., • Response rate after study treatment, is measured according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria. Response rate is defined as a complete response, a partial response, or stable disease, • Progression free survival, defined as the interval between pre-treatment imaging and the earliest occurrence of disease progression, or death, whichever came first. Progression is defined based on the RECIST 1.1 criteria, or the confirmed emerge of local non-primary, metastatic, or nodal disease., • Overall survival, defined as the interval between first study treatment and date of death., • Quality of life measured with QLQ-C30 and EQ-5D

Interventions

DRUGHeparine LEO 5.000 I.E./ml
DRUGoplossing voor injectie
DRUGOMEPRAZOLE
DRUGPANTOPRAZOLE

Sponsors

Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
• The (dose-corrected) difference in intra-tumoral total platinum concentrations following administration of HAI oxaliplatin versus IV oxaliplatin—

Secondary

MeasureTime frame
• Difference in intra-tumoral total platinum concentration following HAI 130 mg/m² versus HAI 85 mg/m²., • Difference in non-tumorous liver tissue total platinum concentration following IV 85 mg/m² versus HAI 85 mg/m²., • Difference in non-tumorous liver tissue total platinum concentration following HAI 130 mg/m² versus HAI 85 mg/m²., • Systemic pharmacokinetic parameters of total platinum, including plasma levels, Cmax, Tmax, Area Under the Curve (AUC), t1/2, Cl, Vd after administration of oxaliplatin via intravenous infusion versus via hepatic arterial infusion., • Incidence and grade of adverse events per treatment cycle and cumulative over the entire treatment period according to NCI CTCAE v6.0, • Post-procedural complications according to the modified CIRSE classification., • Feasibility parameters including completion rate of all planned oxaliplatin administrations and liver biopsies, technical success of HAI procedures, adherence to scheduled blood sampling, need for dose modifi—

Outcome results

None listed

Source: EU CTIS · Data processed: Oct 8, 2026