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

NCT03209492 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 333

Last updated 2019-04-11

Study results available
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Summary

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

Conditions

Interventions

DRUG

Leuprorelin acetate

Leuplin PRO for Injection Kit 22.5 mg

Sponsors & Collaborators

Principal Investigators

  • Study Director · Takeda

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-01
Primary Completion
2017-12-01
Completion
2017-12-01

Countries

  • Japan

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03209492 on ClinicalTrials.gov