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OncoMatch/Clinical Trials/NCT07107334

A Study to Estimate Early Clinical Efficacy Signals of GLP-1 Agonist Administration in Conjunction With Levonorgestrel Intrauterine Device in Obese Patients With Endometrioid Intraepithelial Neoplasia

Is NCT07107334 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Glucagon-like peptide 1 receptor agonist for endometrioid endometrial adenocarcinoma.

Phase 2RecruitingUniversity of FloridaNCT07107334Data as of May 2026

Treatment: Glucagon-like peptide 1 receptor agonistThis study will explore the use of glucagon-like peptide 1 receptor agonist (GLP-1RA) used concurrently with levonorgestrel intrauterine device in patients with poor surgical candidacy for a hysterectomy or patients who are pursuing fertility sparing. GLP-1RA are a class of medications that mimic the natural hormone glucagon-like peptide-1. These medications trigger the pancreas to release insulin which can help lower blood sugar levels and delay gastric emptying. The recent FDA approval of GLP-1RAs has changed the landscape for pharmacotherapy for weight loss. These hormone-based obesity medications are novel and revolutionary in obesity medicine. Liraglutine, semaglutide, and tirzepatide have become exceedingly popular for their effects on weight loss and obesity-related comorbidities. More recently, GLP-1RAs have exhibited risk reduction of various obesity associated cancers, including endometrial cancer but their exact role in prevention and treatment has yet to be measured.

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Extracted eligibility criteria

Cancer type

Endometrial Cancer

Biomarker criteria

Required: ESR1 positive

Disease stage

Grade: 1

No extrauterine involvement or myometrial invasion by MRI (preferred) or transvaginal ultrasound with in the last 3 months

Performance status

ECOG 0–3(Limited self-care)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of Florida · Gainesville, Florida

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