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Clinical Trials in the EU / 2026-527163-15-00
Authorised Phase I/II

ROSETTA RCC-208: A Phase 1/2 Open-label, Multi-center, Randomized Study of Pumitamig Alone or in Combination with Ipilimumab or Cabozantinib in Participants with Advanced Renal Cell Carcinoma (RCC)

2026-527163-15-00 · tracked via the Priya Life Science EU tracker
Sponsor
Bristol-Myers Squibb Services Unlimited Company
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
24/09/2026
Enrollment target
9
Sites
Finland

Condition studied

Advanced Renal Cell Carcinoma

Investigational medicinal product(s)

IPILIMUMABIpilimumabCABOZANTINIBCABOZANTINIBBNT327 50 mg mlBNT327 20 mg ml

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

Phase 1: The main goal of phase 1 will check and count for how many people have side-effects or serious side-effects from the medicine, if anyone must stop taking it because of these side-effects , and if any side-effects cause death., Phase 2: The main goal of phase 2 will be to check and count how many people's kidney cancer gets much smaller or completely goes away with the treatment (OR (Objective Response) (confirmed CR (complete response) or PR (partial response)).

Endpoint detail

Count how many people have side-effects or serious side-effects from the medicines, including those who stop treatment or die because of them (safety)., See how long people live without the cancer getting worse, and how long the cancer stays smaller or goes away (progression delay (PFS, Progression-Free Survival and duration (DOR, Duration of Response).

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-527163-15-00 on CTIS ↗ ← All trials in the EU