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Clinical Trials in the EU / 2025-524090-16-00
Completed Phase I/II

A Phase 1/2 Study of BMS-986525 as Monotherapy and in Combination with Nivolumab in Participants with Relapsed/Refractory Small Cell Lung Cancer

2025-524090-16-00 · tracked via the Priya Life Science EU tracker
Sponsor
Bristol-Myers Squibb Services Unlimited Company
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
18/05/2026
Enrollment target
21
Sites
Italy, Spain, Romania

Condition studied

Relapsed/Refractory Small Cell Lung Cancer

Investigational medicinal product(s)

BMS-986525OPDIVO 10 mg/mL concentrate for solution for infusion.

Eligibility

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

Primary endpoint

Type, frequency, and severity of side effects.

Endpoint detail

How BMS-986525 behaves in the body alone and in combination with nivolumab;, How disease responds to BMS-986525 alone or in combination with nivolumab.

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 2025-524090-16-00 on CTIS ↗ ← All trials in the EU