LivingGLP1
Study S000730

A Pilot Study to Estimate Early Clinical Efficacy Signals of a Glucagon-like Peptide 1 Receptor Agonist (GLP-1RA) Administration in Conjunction With Levonorgestrel Intrauterine Device (LNG-IUD) in Obese Patients With Endometrioid Intraepithelial Neoplasia

Registration

Registration
NCT07107334
Study type
INTERVENTIONAL
Phase
PHASE2
Masking
NONE
Status
RECRUITING
Enrollment
20
Start
2026-04-07
Primary completion
2028-11
Lead sponsor
University of Florida
Conditions
Endometrioid Endometrial Adenocarcinoma
Interventions
DRUG:Glucagon-like peptide 1 receptor agonist
Results posted
FALSE

Registered primary outcomes

  • Time from start of GLP-1RA to clearance of staging hysterectomy [12 months]
  • Time from start of GLP-1RA to clearance for pregnancy pursuit [12 months]
  • Endometrial pathologic response [6 months after beginning GLP-1RA treatment]
  • Endometrial pathologic response [12 months after beginning GLP-1RA treatment]

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