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Safety, Tolerability, and Efficacy of Two Different Oral Doses of NP031112 Versus Placebo in the Treatment of Patients With Mild-to-Moderate Progressive Supranuclear Palsy
NCT01049399 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine wether NP031112 is safe and effective in the treatment of mild to moderate Progressive Supranuclear Palsy
Conditions Studied
Interventions
- DRUG placebo
- DRUG tideglusib
Study Locations (20)
Other
- Neurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson Beelitz — Beelitz-Heilstätten
- Humboldt Universitat Charite, Campus Virchow, Neurologisch — Berlin
- Universitatsklinikum Carl-Guslav-Carus, Technische Universitat Dresden, Klinik und Poliklinik fur Neurologie — Dresden
- Medizinische Hochschule Hannover, Neurologie 0E 7210 — Hanover
- Zentrum fur Nervenheilkunde. Klinik fur Neurologie mit Poliklinik. — Marburg
- University Hospital Tuebingen,Eberhard-Karls-Universitat, Universitatsklinikum Neurologie — Tübingen
- Hospital de Cruces — Barakaldo
- Dpto.neurologia. H. Clinic. — Barcelona
- Hospital de Donostia — Donostia / San Sebastian
- Dpt. Neurologia. Hospital Ramón y Cajal. — Madrid
- Hospital U. La Paz — Madrid
- Hospital Mutua Terrassa — Terrassa
California
- The Parkinson's and Movement Disorder Institute — Fountain Valley
- Department of Neurology, David Geffen School of Medicine at UCLA — Los Angeles
Florida
- Mayo Clinic Jacksonville — Jacksonville
- University of South Florida 5 — Tampa
Kentucky
- Division of Movement Disorders, University of Louisville — Louisville
New Jersey
- University of Medicine and Dentistry, Robert Wood Johnson Medical School — New Brunswick
Barcelona
- Fundació Ace — Barcelona
Madrid
- Hospital Puerta del Hierro — Madrid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2009-12 |
| Est. Completion | 2011-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01049399
The ClinicalTrials.gov registry entry for NCT01049399 describes a study currently listed as completed. It is categorized as NA, 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 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Noscira, which has 1 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 Progressive Supranuclear Palsy 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: NCT01049399 reports 20 study locations spanning 7 distinct geographic areas — top geographies include Other, California, Florida. 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 NCT01049399 about?
NCT01049399 is a clinical study titled "Safety, Tolerability, and Efficacy of Two Different Oral Doses of NP031112 Versus Placebo in the Treatment of Patients With Mild-to-Moderate Progressive Supranuclear Palsy". The purpose of this study is to determine wether NP031112 is safe and effective in the treatment of mild to moderate Progressive Supranuclear Palsy
What is the current status of trial NCT01049399?
This trial is currently completed. It is a NA study. The enrollment target is 146 participants. The study started on 2009-12. Estimated completion is 2011-11.
What conditions does trial NCT01049399 study?
This clinical trial studies the following conditions: Progressive Supranuclear Palsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01049399?
The interventions under investigation include: placebo (DRUG), tideglusib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01049399?
This trial is sponsored by Noscira, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01049399 being conducted?
This trial has 20 study locations across California, Florida, Kentucky, New Jersey, Barcelona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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