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Completed Phase 2 Interventional Results available

Randomized, Placebo Controlled Study Of The Efficacy And Safety Of PF-02545920 In Subjects With Huntington's Disease

ClinicalTrials.gov ID: NCT02197130

Public ClinicalTrials.gov record NCT02197130. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 10:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Placebo Controlled, Double Blind Proof-of-concept Study Of The Efficacy And Safety Of Pf-02545920 In Subjects With Huntington's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is a 26 week, randomized, parallel group, double blind comparison of PF-02545920 5 mg, PF-02545920 20 mg, and placebo dosed BID in the treatment of motor impairment of subjects with Huntington's Disease. A total of approximately 260 subjects are planned to be randomized in the study. Primary endpoint is the change from baseline in the Total Motor Score (TMS) assessment of the Unified Huntington Disease Rating Scale (UHDRS) after 26 weeks of treatment. secondary endpoints will include change from baseline in the Total Maximum Chorea (TMC) score of the UHDRS after 13 and 26 weeks of treatment and Clinical Global Impression-Improvement score after 13 and 26 weeks of treatment.

Study identification

NCT ID
NCT02197130
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
272 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
30 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2014
Primary completion
Aug 31, 2016
Completion
Sep 30, 2016
Last update posted
Nov 16, 2017

2014 – 2016

United States locations

U.S. sites
22
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
The Kirklin Clinic of UAB Hospital Birmingham Alabama 35233
The University of Alabama at Birmingham Birmingham Alabama 35233
University of Alabama at Birmingham Birmingham Alabama 35233
Mayo Clinic Arizona Phoenix Arizona 85054
Mayo Clinic Arizona Scottsdale Arizona 85259
University of California, Irvine Irvine California 92697
Ronald Regan UCLA Medical Center Drug Information Center Los Angeles California 90095
UCLA Neurology Clinic Los Angeles California 90095
UCLA Radiology Los Angeles California 90095
Rocky Mountain Movement Disorders Center Englewood Colorado 80113
University of Florida Center for Movement Disorders and Neurorestoration Gainesville Florida 32607
Indiana University Health Neuroscience Center Indianapolis Indiana 46202
Massachusetts General Hospital Charlestown Massachusetts 02129
Washington University School of Medicine St Louis Missouri 63110
Albany Medical College Albany New York 12208
Wake Forest Baptist Medical Center - Dept. of Neurology Winston-Salem North Carolina 27157
Cleveland Clinic Foundation Hospital Pharmacy Cleveland Ohio 44195
The Cleveland Clinic Foundation Cleveland Ohio 44195
Davis Medical Center Columbus Ohio 43210
The Wexner Medical Center at the Ohio State University Columbus Ohio 43221
Wexner Medical Center at the Ohio State University Columbus Ohio 43221
Baylor College of Medicine Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02197130, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 16, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02197130 live on ClinicalTrials.gov.

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