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leuprolide

Generic: LEUPROLIDE MESYLATE·Brand: CAMCEVI ETM, CAMCEVI KIT, Camcevi, ELIGARD KIT, Eligard, FENSOLVI KIT, Fensolvi, LEUPROLIDE ACETATE, LEUPROLIDE ACETATE FOR DEPOT SUSPENSION, LUPRON, LUPRON DEPOT, LUPRON DEPOT-PED KIT, Lupron, Lutrate, VIADUR, Vabrinty

leuprolide: 21 clinical trials tracked.

leuprolide evidence translation

What we can confirm

21 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about leuprolide, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 7 study sponsors
Clinical Trials (21)showing 10 most recent

Neoadjuvant ADT and Darolutamide With Pembrolizumab, Followed by Adjuvant Pembrolizumab in NCCN High-risk and Molecularly Stratified Prostate Cancer Patients

NCT07027124·Phase 2
Recruiting

Primary endpoint: Proportion of patients who achieve Minimal residual disease (MRD)

Interventionalopen40 targetStarted 2026-05Completion 2031-051 site · United StatesIcahn School of Medicine at Mount Sinai

Phase 2 Randomized Trial to Examine Ovarian Function Suppression for Breast Cancer (OFS)

NCT07158021·Phase 2·MYOV
Recruiting

Primary endpoint: Proportion of participants with ultrasensitive estradiol concentration > 10 pg/ml

InterventionalRandomizedopen75 targetStarted 2026-01Completion 2028-011 site · United StatesUniversity of Michigan Rogel Cancer Center

A Randomized Trial of Neoadjuvant Leuprorelin, Darolutamide or Both Prior to Radical Prostatectomy for Intermediate or High-risk Prostate Cancer

NCT06627530·Phase 4·MYOV
Active, not recruiting

Primary endpoint: Proportion of patients with minimal residual disease

InterventionalRandomizedsingle144 targetStarted 2025-02Completion 2026-096 sites · BrazilBrazilian Clinical Research Institute

Randomized Controlled Trial of Leuprolide Plus Abiraterone Acetate (AA) Versus Relugolix Plus AA for Advanced Prostate Cancer: The REVELUTION-2 Trial

NCT06650579·Phase 3
Recruiting

Primary endpoint: Incidence of ambulatory systolic blood pressure (BP) > 140 or diastolic > 90 (measurement on 2 separate days)

InterventionalRandomizeddouble72 targetStarted 2025-01Completion 2029-074 sites · United StatesEmory University

A Comparison of Orgovyx (Relugolix) vs Eligard (Leuprolide) on Cardiovascular Function and Biomarkers During Standard of Care Combined ADT (Androgen Deprivation Therapy)-Radiation for Prostate Cancer

NCT06330805·Phase 2
Recruiting

Primary endpoint: Physiologic alterations in cardiopulmonary function - Myocardial perfusion

InterventionalRandomizedopen70 targetStarted 2024-08Completion 2027-121 site · United StatesOhio State University Comprehensive Cancer Center

MC230502 Dynamic Investigator Initiated Enterprise (DIVINE) in Prostate Cancer

NCT06378866·Phase 2·KYNB
Recruiting

Primary endpoint: Modified radiographic progression-free survival (mrPFS) (Groups A & B)

InterventionalRandomizedopen532 targetStarted 2024-06Completion 2029-053 sites · United StatesMayo Clinic

A Phase IIIb Study to Characterize the Efficacy and Safety of Adjuvant Ribociclib Plus Endocrine Therapy in a Close-to-clinical Practice Patient Population With HR+ HER2- Early Breast Cancer (Adjuvant WIDER)

NCT05827081·Phase 3·NVS
Recruiting

Primary endpoint: Invasive Breast Cancer Free Survival (iBCFS) rate at 3 years

Interventionalopen1,400 targetStarted 2024-02Completion 2030-0950 sites · United StatesNovartis Pharmaceuticals

RecoverPC: A Phase 2 Study of RElugolix Versus GnRH Agonist Quality of Life (QOL) and Testosterone reCOVERy in Men With Prostate Cancer

NCT05765500·Phase 2
Recruiting

Primary endpoint: 9-month Quality of Life (QOL) Score

InterventionalRandomizedsingle110 targetStarted 2024-02Completion 2028-013 sites · United StatesDana-Farber Cancer Institute

An Open-label, Single Arm, Multicenter, Phase III Study on the Efficacy, Safety, and Pharmacokinetics of FP-001 42 mg Controlled Release in Patients With Central (Gonadotropin-Dependent) Precocious Puberty (Casppian Study)

NCT05493709·Phase 3
Completed

Primary endpoint: Efficacy of Leuprolide Mesylate (FP-001 42 mg)

Interventionalopen94 enrolledStarted 2023-06Completion 2026-0541 sites · China, Puerto Rico, Taiwan, United StatesForesee Pharmaceuticals Co., Ltd.

Real World Evidence Study on Metastatic Prostate Cancer Patient Characteristics, Treatment Patterns and Outcomes in the Pirkanmaa Hospital District in Finland

Completed

Primary endpoint: Body Mass Index (BMI)

Observational1,083 enrolledStarted 2023-02Completion 2024-041 site · FinlandPfizer