Trial NCT00683917

View at ClinicalTrials.gov 
Org. Study IDs: ZPU-202

Last trial update was posted on 2014-08-21

MeSH Interventions

Leuprolide

MeSH Conditions

Leiomyoma Myofibroma

Other Conditions

Uterine Fibroids

Stopping Reasons

Repros stopped the study for safety and FDA put the study on hold for safety.

Limitations And Caveats

The study was prematurely terminated for safety reasons (Proellex studies were put on clinical hold due to liver toxicity). Sponsor was unable to pay vendor, and was therefore not provided with any study data.

Result Publications

N/A

Annotations

Category Annotations
No annotators decided on categories yet

Intervention Annotations
# Outdated Intervention Condition
Name Route DrugBank ID