A Study of Sacituzumab Govitecan (IMMU-132) in Platinum-resistant Ovarian Cancer Patients

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

January 8, 2024

Primary Completion Date

November 1, 2026

Study Completion Date

November 1, 2027

Conditions
Ovarian Carcinoma
Interventions
DRUG

Sacituzumab govitecan

Sacituzumab govitecan will be administered at 10 mg/kg weekly as an infusion for 2 consecutive weeks (2 weekly doses plus 1 week without treatment represents a single 3 week cycle). Treatment can be continued without a rest period in the absence of progression of disease or unacceptable toxicity.

Trial Locations (1)

06510

Smilow Cancer Hospital at Yale New Haven, New Haven

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Gilead Sciences

INDUSTRY

lead

Yale University

OTHER