Observational, Postmarketing Surveillance Study of Spinraza Injection (Nusinersen Sodium)

NCT04317794 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 74

Last updated 2025-07-17

No results posted yet for this study

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

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

More Related Trials

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 NCT04317794 on ClinicalTrials.gov