Last reviewed · How we verify

NCT03209479

Copaxone Subcutaneous Injection Syringe Special Drug Use-Result Investigation (All-Case Investigation) "Prevention of Relapse of Multiple Sclerosis"

Completed Last updated 13 June 2024
What this trial tests

trial testing Glatiramer acetate in Multiple Sclerosis in 1,332 participants. Completed in 31 March 2024.

Timeline
24 November 2015
Primary endpoint
31 March 2024
31 March 2024

Quick facts

Lead sponsorTeva Takeda Pharma Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,332
Start date24 November 2015
Primary completion31 March 2024
Estimated completion31 March 2024
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Teva Takeda Pharma Ltd.

Who can join

Eligibility, any sex, with Multiple Sclerosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the safety and efficacy of Copaxone subcutaneous injection syringe (hereinafter referred to as Copaxone) in patients with multiple sclerosis in the routine clinical setting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Glatiramer acetate

Trials testing the same drug.

Other recruiting trials for Multiple Sclerosis

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03209479.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing