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A Trial to Test if TEV-56286 is Effective for Treatment of Participants With Multiple System Atrophy
NCT06568237 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG TEV-56286
Study Locations (20)
California
- Teva Investigational Site 15554 — La Jolla
- Teva Investigational Site 15545 — Los Angeles
Florida
- Teva Investigational Site 15544 — Boca Raton
- Teva Investigational Site 15555 — Tampa
New York
- Teva Investigational Site 15549 — New York
- Teva Investigational Site 15551 — New York
Pennsylvania
- Teva Investigational Site 15735 — Hershey
- Teva Investigational Site 15548 — Pittsburgh
Other
- Teva Investigational Site 35290 — Bordeaux
- Teva Investigational Site 35289 — Marseille
District of Columbia
- Teva Investigational Site 15547 — Washington D.C.
Illinois
- Teva Investigational Site 15550 — Chicago
Kansas
- Teva Investigational Site 15546 — Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 350 participants |
| Start Date | 2024-10-02 |
| Est. Completion | 2027-09-15 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06568237
The ClinicalTrials.gov registry entry for NCT06568237 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Multiple System Atrophy appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06568237 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Florida, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06568237 about?
NCT06568237 is a clinical study titled "A Trial to Test if TEV-56286 is Effective for Treatment of Participants With Multiple System Atrophy". 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...
What is the current status of trial NCT06568237?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 350 participants. The study started on 2024-10-02. Estimated completion is 2027-09-15.
What conditions does trial NCT06568237 study?
This clinical trial studies the following conditions: Multiple System Atrophy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06568237?
The interventions under investigation include: Placebo (DRUG), TEV-56286 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06568237?
This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06568237 being conducted?
This trial has 20 study locations across California, District of Columbia, Florida, Illinois, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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