Clinical Trial

Investigation of Ubamatamab Combination Therapy in Adult Participants With Platinum-Resistant Ovarian Cancer

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
This study is researching an experimental drug called ubamatamab, also referred to as "study drug". The study is focused on participants who have advanced ovarian cancer. The aim of the study is to see how safe, tolerable, and effective the study drug is on its own and in combination with other anti-cancer drugs (bevacizumab, cemiplimab, fianlimab, REGN10597 and a standard chemotherapy drug, pegylated liposomal doxorubicin \[PLD\]), referred to as "combination drugs'. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug and its experimental combinations * How much study drug and fianlimab is in the blood at different times * Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects) and its combinations
Protocol Amendment History 5 changes
notable Enrollment increased: 220 -> 297 participants 2026-08-13
minor Trial arms changed: 5 -> 6 2026-08-13
notable Primary completion moved earlier: 2028-10-30 -> 2028-06-30 2026-08-13
minor Completion moved earlier: 2028-10-30 -> 2028-06-30 2026-08-13
notable Trial sites expanded: 47 -> 50 locations 2026-04-09
Trial Details
NCT Number NCT06787612
Lead Sponsor Regeneron Pharmaceuticals
Conditions Ovarian Cancer, Fallopian Tube Cancer, Primary Peritoneal Cancer
Enrollment 297 participants
Start Date 2025-05-28
Primary Completion 2028-06-30 (estimated)
Study Completion 2028-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-08-12