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Study to Evaluate the Safety and Efficacy of Davunetide for the Treatment of Progressive Supranuclear Palsy
NCT01110720 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the study is to evaluate the safety and efficacy of davunetide for the treatment of Progressive Supranuclear Palsy.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Davunetide
Study Locations (20)
California
- USC Keck School of Medicine — Los Angeles
- David Geffen School of Medicine - UCLA — Los Angeles
- UCSD/VA Neurology Service — San Diego
- UCSF Memory and Aging Center — San Francisco
Florida
- Parkinson's Disease and Movement Disorders Center of Boca Raton — Boca Raton
- Mayo Clinic, Florida — Jacksonville
- The Frances J. Zesiewicz Foundation for Parkinson's Disease at USF — Tampa
Arizona
- Muhammed Ali Parkinson Center and Movement Disorders Clinic — Phoenix
- Mayo Clinic, AZ — Scottsdale
Massachusetts
- Massachusetts General Hospital — Boston
- Lahey Clinic — Burlington
Minnesota
- University of Minnesota Department of Neuology — Minneapolis
- Mayo Clinic, Rochester, MN — Rochester
Alabama
- University of Alabama - Birmingham — Birmingham
Colorado
- Colorado Neurological Institute - Rocky Mountain Movement Disorders Ctr, PC — Englewood
Illinois
- University of Chicago Medical Center — Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 313 participants |
| Start Date | 2010-10 |
| Est. Completion | 2012-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01110720
The ClinicalTrials.gov registry entry for NCT01110720 describes a study currently listed as completed. 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 313 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allon Therapeutics, which has 2 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: NCT01110720 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT01110720 about?
NCT01110720 is a clinical study titled "Study to Evaluate the Safety and Efficacy of Davunetide for the Treatment of Progressive Supranuclear Palsy". The purpose of the study is to evaluate the safety and efficacy of davunetide for the treatment of Progressive Supranuclear Palsy.
What is the current status of trial NCT01110720?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 313 participants. The study started on 2010-10. Estimated completion is 2012-12.
What conditions does trial NCT01110720 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 NCT01110720?
The interventions under investigation include: Placebo (DRUG), Davunetide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01110720?
This trial is sponsored by Allon Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01110720 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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