Specified Drug-Use Survey of Leuprorelin Acetate Injection Kit 11.25 mg "All-Case Investigation: Spinal and Bulbar Muscular Atrophy (SBMA)"

NCT03555578 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1905

Last updated 2026-05-22

No results posted yet for this study

Summary

The purpose of this survey is to evaluate the long-term safety and efficacy of leuprorelin acetate injection kit 11.25 mg in patients with spinal and bulbar muscular atrophy (SBMA) in the routine clinical setting.

Conditions

  • Spinal and Bulbar Muscular Atrophy

Interventions

DRUG

Leuprorelin Acetate

Leuprorelin Acetate Injection Kit

Sponsors & Collaborators

Principal Investigators

  • Study Director · Takeda

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-02
Primary Completion
2026-04-30
Completion
2026-04-30

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 NCT03555578 on ClinicalTrials.gov