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Clinical Trials in the EU / 2023-509535-11-00
Authorised Phase II

Use of the Checkpoint inhibitor DOstarlimab in the endOmetrial cancer fertility-Sparing trEatment: CHOOSE study.

2023-509535-11-00 · tracked via the Priya Life Science EU tracker
Sponsor
UZ Leuven
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Neoplasms
Decision date
23/09/2026
Enrollment target
5
Sites
Belgium

Condition studied

Newly diagnosed endometrial carcinomas of the MMR-deficient molecular subtype

Investigational medicinal product(s)

DOSTARLIMAB

Eligibility

Age group
18-64 years
Sex
Female

Primary endpoint

Complete response rate

Endpoint detail

Overall response rate, Time to recurrence, 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 2023-509535-11-00 on CTIS ↗ ← All trials in the EU