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A Single-Arm Clinical Study of Selective Tumor Embolization Combined with Axitinib and Iparomlimab and Tuvonralimab in Metastatic Renal Cell Carcinoma

A Single-Arm Clinical Study of Selective Tumor Embolization Combined with Axitinib and Iparomlimab and Tuvonralimab in Metastatic Renal Cell Carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105741
Enrollment
Unknown
Registered
2025-07-09
Start date
2025-07-09
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Renal Cell Carcinoma

Interventions

Experimental group:Iparomlimab and Tuvonralimab Injection+Axitinib+Selective Tumor Embolization

Sponsors

Tianjin Cancer Hospital Airport Hospita
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age 18-80 years; 2 Histopathologically confirmed clear cell or non-clear cell renal carcinoma; 3 No prior systemic therapy received; 4 ECOG performance status score of 0 or 1; 5 Life expectancy 6 mon>=ths; 6 Voluntarily signed informed consent form.

Exclusion criteria

Exclusion criteria: 1?Inability to comply with the study protocol or procedures; 2?Patients with concurrent malignancies or severe organ dysfunction; 3?Presence of central nervous system (CNS) metastases; 4?Positive anti-HIV test; HBsAg-positive with HBV-DNA > upper limit of normal (ULN); active hepatitis C virus (HCV) infection (HCV RNA-positive); 5?Intolerance to radiotherapy or immunotherapy; 6?Chronic systemic corticosteroid therapy (>7 days) within 7 days prior to first dose; 7?Pregnancy or lactation; 8?Investigator-deemed ineligibility for study participation.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Overall survival, OS;Progression Free Survival, PFS;

Countries

China

Contacts

Public Contactyangqing

Tianjin Cancer Hospital Airport Hospita

zero1234562025@163.com+86 186 2222 1106

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026