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
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
- lead INDUSTRY
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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