Condition: Multiple System Atrophy · Sponsor: Teva Branded Pharmaceutical Products R&D LLC
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.
Teva U.S. Medical Information · 1-888-483-8279 · USMedInfo@tevapharm.com
Always discuss trial participation with your own doctor first.
| Teva Investigational Site 15554 | La Jolla, California, United States | Recruiting |
| Teva Investigational Site 15544 | Boca Raton, Florida, United States | Recruiting |
| Teva Investigational Site 15555 | Tampa, Florida, United States | Recruiting |
| Teva Investigational Site 15549 | New York, New York, United States | Recruiting |
| Teva Investigational Site 15551 | New York, New York, United States | Recruiting |
| Teva Investigational Site 15543 | Spokane, Washington, United States | Recruiting |
| Teva Investigational Site 35290 | Bordeaux, France | Recruiting |
| Teva Investigational Site 35291 | Paris, France | Recruiting |
| Teva Investigational Site 35292 | Toulouse, France | Recruiting |
| Teva Investigational Site 32818 | Dresden, Germany | Recruiting |
| Teva Investigational Site 32822 | Düsseldorf, Germany | Recruiting |
| Teva Investigational Site 32825 | Kassel, Germany | Recruiting |
+ 18 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07197866