Clinical Trials Directory

Trials / Completed

CompletedNCT03209492

Special Drug Use Surveillance of Leuplin PRO for Injection Kit 22.5 mg for "Prostate Cancer"

Status
Completed
Phase
Study type
Observational
Enrollment
333 (actual)
Sponsor
Takeda · Industry
Sex
Male
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety in patients with prostate cancer receiving the drug in the routine clinical setting.

Detailed description

The drug being tested in this study is called Leuprorelin acetate (Leuplin PRO for Injection Kit 22.5 mg). Leuprorelin acetate is being tested to treat people who have prostate cancer. This study will look at the safety in patients with prostate cancer receiving the drug in the routine clinical setting. The study will enroll approximately 300 patients. • Leuprorelin acetate This multi-center trial will be conducted in Japan.

Conditions

Interventions

TypeNameDescription
DRUGLeuprorelin acetateLeuplin PRO for Injection Kit 22.5 mg

Timeline

Start date
2016-04-01
Primary completion
2017-12-01
Completion
2017-12-01
First posted
2017-07-06
Last updated
2019-04-11
Results posted
2019-04-11

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT03209492. Inclusion in this directory is not an endorsement.

Special Drug Use Surveillance of Leuplin PRO for Injection Kit 22.5 mg for "Prostate Cancer" (NCT03209492) · Clinical Trials Directory