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Sponsor: Teva Branded Pharmaceutical Products R&D LLC
Conditions: Multiple System Atrophy
Interventions: TEV-56286, Placebo
Countries: United States, France, Germany, Israel, Italy, Japan, Serbia, Spain
The primary objective of the study is to evaluate the efficacy of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA). A secondary objective of the study is to evaluate specific efficacy parameters of TEV-56286. Another secondary objective is to evaluate the safety and tolerability of TEV-56286. The planned study period per participant is 56 weeks including a screening period (up to 4 weeks), a 48-week double-blind treatment period, and a follow-up visit (approximately 4 weeks after the end of the double-blind treatment period). The study duration will be approximately 27 months.
Sex: ALL
Age: 30 Years to 75 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
Inclusion Criteria: * is considered to be "clinically possible" or "clinically probable" MSA as determined by the Gilman criteria * is medically and psychiatrically stable, as indicated by medical and psychiatric history, as well as physical and neurological examination * Females of child bearing potential (CBP) may be included only if they have a negative pregnancy test at the screening and baseline visits * Females of CBP whose male partners are potentially fertile (ie, no vasectomy) must use highly effective birth control methods * Males who are potentially fertile/reproductively competent (not surgically \[eg, vasectomy\] or congenitally sterile) and their female partners who are of CBP must use, together with their female partners, highly effective birth control methods * Additional criteria apply; please contact the investigator for more information Exclusion Criteria: * has 2 or more relatives with history of MSA, suggestive of an alternative diagnosis other than MSA * has participated in another clinical study involving administration of an IMP within 3 months or 5 half-lives (whichever is longer) of this IMP prior to screening * has a history of, or acknowledges, alcohol or other substance abuse in the 12 months before screening * is a female participant who is pregnant or breastfeeding, or plans to become pregnant during the study * has a known hypersensitivity to any components of the IMP * is of a vulnerable population (eg, people kept in detention or jail) * participant is using or consuming any prohibited concomitant medications within the specified exclusionary windows of this study * Additional criteria apply; please contact the investigator for more information
- La Jolla, California, United States
- Los Angeles, California, United States
- Washington D.C., District of Columbia, United States
- Boca Raton, Florida, United States
- Tampa, Florida, United States
- Chicago, Illinois, United States
- Kansas City, Kansas, United States
- Boston, Massachusetts, United States
- Farmington Hills, Michigan, United States
- Rochester, Minnesota, United States
- New York, New York, United States
- New York, New York, United States
- Durham, North Carolina, United States
- Hershey, Pennsylvania, United States
- Pittsburgh, Pennsylvania, United States
- Nashville, Tennessee, United States
- Georgetown, Texas, United States
- Alexandria, Virginia, United States
- Spokane, Washington, United States
- Bordeaux, France
- Caen, France
- Marseille, France
- Paris, France
- Toulouse, France
- Beelitz, Germany
- Dresden, Germany
- Düsseldorf, Germany
- Kassel, Germany
- Leipzig, Germany
- Marburg, Germany
- + 31 more on CT.gov