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NCT05675787

Medroxyprogesterone Acetate Plus Atorvastatin in Young Women With Early Endometrial Carcinoma and Atypical Endometrial Hyperplasia

Recruiting now Phase 2 Last updated 11 July 2024
What this trial tests

Phase 2 trial testing Medroxyprogesterone acetate + Atorvastatin in Atypical Endometrial Hyperplasia in 82 participants. Currently enrolling.

Timeline
6 January 2023
Primary endpoint
31 August 2025
31 October 2025

Quick facts

Lead sponsorPeking University People's Hospital
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment82
Start date6 January 2023
Primary completion31 August 2025
Estimated completion31 October 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University People's Hospital

Who can join

Adults 17 to 45, female only, with Atypical Endometrial Hyperplasia or Endometrial Carcinoma Stage I. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To explore the treatment efficacy of medroxyprogesterone acetate plus atorvastatin in patients with atypical endometrial hyperplasia (AEH) and early endometrial carcinoma (EEC) for conservative treatment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Lipid metabolism reprogramming in endometrial cancer: biological functions and therapeutic implications.
    Wang X, Li Y, Hou X, Li J, et al · · 2024 · cited 22× · PMID 39256811 · DOI 10.1186/s12964-024-01792-7

Verify or expand the search:

Other recruiting trials for Atypical Endometrial Hyperplasia

Currently open trials in the same condition.

Other Peking University People's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05675787.

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