WHO ICTRP trial

A Study to Assess Adverse Events and Change in Disease Activity of Multiple…

CTIS2025-521606-18-00 · EU Clinical Trials Information System · Not Recruiting

Key facts

Trial ID CTIS2025-521606-18-00
Public title A Study to Assess Adverse Events and Change in Disease Activity of Multiple Treatment Combinations with Intravenous Mirvetuximab Soravtansine in Adult Participants with Ovarian Cancer
Scientific title A Phase 2, Open-Label, Randomized, Master Protocol Dose Optimization Study to Evaluate Safety and Efficacy of Multiple Treatment Combinations with Mirvetuximab Soravtansine in Subjects with Ovarian Cancer (FLORENZA) - M25-709
Primary sponsor AbbVie Deutschland GmbH & Co. KG
Registry EU Clinical Trials Information System
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): No Therapeutic exploratory (Phase II): Yes Therapeutic confirmatory - (Phase III): No Therapeutic use - (Phase IV): No
Countries Australia;Korea, Republic of;United States;Belgium;Czechia;Denmark;France;Spain
Conditions Ovarian Cancer MedDRA version: 20.0Level: PTClassification code: 10033128Term: Ovarian cancer Class: 100000004864;Therapeutic area: Diseases [C] - Neoplasms [C04]
Interventions Product Name: CARBOPLATIN, Product Code:SUB06614MIG, Pharmaceutical Form: SOLUTION FOR INJECTION, Other descriptive name: , Strength: , Product Name: BEVACIZUMAB, Product Code:SUB16402MIG, Pharmaceutical Form: CONCENTRATE FOR SOLUTION FOR…
Registration date Sep 18, 2025
Target size 320
Secondary IDs NCT07059845
Registry page euclinicaltrials.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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