Metastatic Renal Cell Carcinoma (mRCC)

2

Review clinical trials related to Metastatic Renal Cell Carcinoma (mRCC). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

International Multicentric Study ARON-1

The ARON-1 Study is designed as an International Multicentric Retrospective Study to collect global experiences with the use of immuno-combinations in patients with metastatic RCC. Two Supplementary Studies (ARON-1α and ARON-1β) have been designed. The ARON-1α Supplementary Study has been designed to investigate for the presence of genomic signatures from tumor samples of patients treated with first-line immuno-combinations for advanced RCC. The ARON-1β Supplementary Study has been designed to charaterize the immune cell populations and assess their relationship with the clinical outcome of mRCC patients treated with first-line immuno-combinations

Participants needed: 1,220
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hospital of MacerataUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Patients aged >18y [+3]

Patients without histologically confirmed diagnosis of RCC [+2]

Status: Recruiting

PET/CT-Directed Free of Therapy for Metastatic RCC Patients With IMDC Favorable or Intermediate Risk

This phase 2 trial aims to test the feasibility and efficiency of PET/CT-directed treatment interruption strategy in metastatic renal cell carcinoma patients with IMDC favorable/intermediate risk who achieve complete (CMR) or partial metabolic response (PMR) after ≥12 months of first-line PD-1/PD-L1 Immune checkpoint inhibitor (ICI)+ VEGFR-tyrosine kinase inhibitor (TKI) therapy. It helps figure out whether PET/CT can safely direct treatment pause as well as explores a new individualized treatment option based on metabolic imaging for RCC patients.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Jinling Hospital, ChinaUpdated: Sep 16, 2025Locations: 1
Eligibility criteria

Male or female subjects aged ≥ 18 years at time of signing informed consent [+7]

Highly malignant pathology [+45]