Retrospective, Non-interventional Study of Depo-Eligard®.

NCT00811876 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2010-01-22

No results posted yet for this study

Summary

Study will evaluate the real-world effectiveness of Depo-Eligard® after six months of treatment

Conditions

Interventions

OTHER

Data Collection on Depo-Eligard exposure

Retrospective, Non-interventional

Sponsors & Collaborators

  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • Use Central Contact · Astellas Pharma Europe B.V.

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2009-12-31
Completion
2009-12-31

Countries

  • Belgium

Study Locations

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Entities

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 NCT00811876 on ClinicalTrials.gov