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Study identifier: NCT07197866 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

An Extension Trial to Test if TEV-56286 is Effective in Relieving Multiple System Atrophy

Condition: Multiple System Atrophy  ·  Sponsor: Teva Branded Pharmaceutical Products R&D LLC

PhasePhase 2
Planned participants200
Who can joinAll sexes, 30 Years to no upper limit
Healthy volunteersNo

About this study

The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA). A secondary objective of the trial is to further describe the safety and tolerability of TEV-56286. The planned total duration of the trial is approximately 100 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Teva U.S. Medical Information  ·  1-888-483-8279  ·  USMedInfo@tevapharm.com

Always discuss trial participation with your own doctor first.

Locations (30)

Teva Investigational Site 15554La Jolla, California, United StatesRecruiting
Teva Investigational Site 15544Boca Raton, Florida, United StatesRecruiting
Teva Investigational Site 15555Tampa, Florida, United StatesRecruiting
Teva Investigational Site 15549New York, New York, United StatesRecruiting
Teva Investigational Site 15551New York, New York, United StatesRecruiting
Teva Investigational Site 15543Spokane, Washington, United StatesRecruiting
Teva Investigational Site 35290Bordeaux, FranceRecruiting
Teva Investigational Site 35291Paris, FranceRecruiting
Teva Investigational Site 35292Toulouse, FranceRecruiting
Teva Investigational Site 32818Dresden, GermanyRecruiting
Teva Investigational Site 32822Düsseldorf, GermanyRecruiting
Teva Investigational Site 32825Kassel, GermanyRecruiting

+ 18 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07197866