Leuprolide: clinical trials recruiting now
7
Recruiting trials
15
Conditions studied
40
US states with sites
16
Countries
FDA drug label
- FDA-approved
- Yes. Leuprolide appears in the FDA drug-label database. Marketed as CAMCEVI.
FDA-approved use
CAMCEVI is indicated for the treatment of adult patients with advanced prostate cancer. CAMCEVI is a gonadotropin-releasing hormone (GnRH) agonist indicated for the treatment of adult patients with advanced prostate cancer.
Phase breakdown
Phase 2 5
Phase 3 2
Conditions being studied
Recruiting trials involving Leuprolide
- Assessing Efficacy of Neoadjuvant ADT in Localized High-Risk Prostate Cancer Patients Utilizing 18F-Flotufolastat PSMA PET/CT
- Effects of Relugolix vs Leuprolide on Cardiac Function in Patients With Prostate Cancer
- Leuprolide and Goserelin for Ovarian Function Suppression in Pre- or Peri-menopausal Women With Breast Cancer, OFS Trial
- Phase IIIb Study of Ribociclib + ET in Early Breast Cancer
- REVELUTION-2: Relugolix+Abiraterone Acetate (AA) Versus Leuprolide+AA Cardiac Trial
- RecoverPC: Relugolix vs GnRH Agonist in Quality of Life
- Stereotactic Body Radiation Therapy Plus Immediate or Delayed Androgen Receptor Pathway Inhibitor and Androgen Deprivation Therapy or Salvage Radiation Therapy for the Treatment of Prostate Cancer, DIVINE Trial
Common questions
Is Leuprolide FDA-approved?
Yes, marketed as CAMCEVI.
How many recruiting trials involve Leuprolide?
7 recruiting trials across 15 conditions.
Is this list of trials complete?
No. For the full record, search ClinicalTrials.gov.