EligibleTrials

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.

FDA label via openFDA

Phase breakdown

Phase 2 5 Phase 3 2

Conditions being studied

ConditionTrials
Prostate Cancer · Leuprolide for Prostate Cancer5
Breast cancer2
Anatomic Stage I Breast Cancer AJCC v81
Anatomic Stage II Breast Cancer AJCC v81
Anatomic Stage III Breast Cancer AJCC v81
Anatomic Stage IV Breast Cancer AJCC v81
Biochemically Recurrent Prostate Carcinoma1
Castration-resistant Prostate Cancer1
Early Breast Cancer1
Localized Prostate Carcinoma1
Metastatic Breast Carcinoma1
Prostate Adenocarcinoma1
Prostatic Neoplasms1
Recurrent Castration-Sensitive Prostate Carcinoma1
Recurrent Prostate Cancer1

Recruiting trials involving Leuprolide

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.

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