OncoMatch/Clinical Trials/NCT07166094
Study to Assess the Efficacy and Safety of Rina-S Compared to Treatment of Investigator's Choice in Participants With Endometrial Cancer
Is NCT07166094 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including Rina-S and IC for endometrial cancer.
Treatment: Rina-S · IC — The purpose of this study is to compare how well Rina-S (GEN1184) works compared to treatment of physician's choice (paclitaxel or doxorubicin) that are considered standard medical care for the treatment of recurrent or progressive endometrial cancer (EC) following prior therapy. There is an equal (50:50) chance of getting either Rina-S or a chemotherapy agent as treatment in this study. The study duration will be approximately 3 years. The treatment duration will be different for every participant, but an average of 4 to 6 months is expected. All participants will receive active drug; no one will be given placebo. Participation in the study will require visits to the study site(s).
Check if I qualifyExtracted eligibility criteria
Cancer type
Endometrial Cancer
Prior therapy
Must have received: platinum-based chemotherapy
Participants must have received prior platinum-based chemotherapy
Must have received: anti-PD-1 therapy
Participants must have received prior...programmed death (ligand)-1 (PD(L)-1) inhibitor, either separately or in combination
Cannot have received: antibody-drug conjugate
Exception: containing a topoisomerase 1 inhibitor
Prior therapy with an antibody-drug conjugate containing a topoisomerase 1 inhibitor
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- SMH - Sarasota - Main Campus · Sarasota, Florida
- Emory Winship Cancer Inst. · Atlanta, Georgia
- Emory Winship Cancer Inst. · Atlanta, Georgia
- Emory Winship Cancer Inst./Emory Decatur Hospital · Decatur, Georgia
- Trials365, LLC · Shreveport, Louisiana
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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