Observational, Postmarketing Surveillance Study of Spinraza Injection (Nusinersen Sodium)
NCT04317794 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 74
Last updated 2025-07-17
Summary
The primary objective is to evaluate the safety of nusinersen sodium injection in the postmarketing setting in Korea. The secondary objective is to evaluate the effectiveness of nusinersen sodium injection in the postmarketing setting in Korea.
Conditions
- Muscular Atrophy, Spinal
Interventions
- DRUG
-
Nusinersen Sodium Injection
Administered as specified in the treatment arm.
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Medical Director · Biogen
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-07-02
- Primary Completion
- 2027-02-05
- Completion
- 2027-02-05
Countries
- South Korea
Study Locations
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