drugset / Trial / NCT06914297

TQB2450 Plus Progestin for Fertility-sparing Treatment in MMRd EC

NCT06914297

Phase 2 Recruiting 10 enrolled Fudan University
NaSingle-groupOpen-labelTreatment

Summary

Based on the above situation, the investigators propose the following scientific hypothesis: In young patients with early MMRd type EC, the use of immune checkpoint inhibitors combined with progesterone for fertility retention therapy can improve the therapeutic efficacy, reduce recurrence, and improve tumor prognosis. Based on the above assumptions, this project intends to conduct a prospective exploratory clinical study in EC patients limited to the endometrial layer or superficial myometrium (FIGO 2023 IA1-IA2 stage). The subjects were treated with TQB2450 periodic intravenous drip + high-potency progesterone daily oral therapy. During the treatment period, hysteroscopy was performed every 12 weeks to evaluate the therapeutic efficacy. The primary endpoint was the 12-week CR rate; the secondary endpoints included the 24-week CR rate, the 36-week CR rate, the median CR time, the 1-year relapse rate, the 2-year relapse rate, the median relapse time, the pregnancy rate, the live birth rate, and drug-related adverse reactions. The exploratory indicators were the response of different MMRd tumors to immune checkpoint inhibitors and their possible mechanisms. The development of this study will provide a clinical basis for improving the fertility-preserving treatment regimen of MMRd EC.

Timeline

Start
2025-04-21
Primary completion
2027-10-01
Completion
2029-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Benmelstobart Monoclonal antibody 1200 mg Intravenous
Subject Megestrol Acetate Other / unclassified 160 mg Oral
Subject Megestrol Acetate Other / unclassified 500 mg Oral
Subject medroxyprogesterone acetate Other / unclassified 500 mg Oral
Subject meprogesterone acetate Unknown 160 mg Oral

Indications