Non-Interventional, Postmarketing Surveillance Study of Nusinersen Sodium Injection

NCT04419233 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2023-12-07

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the safety of nusinersen sodium injection in the postmarketing setting in China.The secondary objectives are to collect data on the efficacy and the pharmacokinetics of nusinersen sodium injection in the post-marketing setting in China.

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
2020-11-18
Primary Completion
2023-11-21
Completion
2023-11-21

Countries

  • China

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 NCT04419233 on ClinicalTrials.gov