ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Alternatives for Reducing Chorea in Huntington Disease

ClinicalTrials.gov ID: NCT01897896

Public ClinicalTrials.gov record NCT01897896. 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 May 7, 2026, 9:04 AM EDT

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

Official title

An Open-Label, Long Term Safety Study of SD-809 ER in Subjects With Chorea Associated With Huntington Disease

Study identification

NCT ID
NCT01897896
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Auspex Pharmaceuticals, Inc.
Industry
Enrollment
119 participants

Conditions and interventions

Interventions

  • SD-809 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 11, 2013
Primary completion
Aug 20, 2017
Completion
Aug 20, 2017
Last update posted
Nov 8, 2021

2013 – 2017

United States locations

U.S. sites
34
U.S. states
25
U.S. cities
33
Facility City State ZIP Site status
Teva Investigational Site 057 Birmingham Alabama 35233
Teva Investigational Site 038 Phoenix Arizona 85013
Teva Investigational Site 298 Fayetteville Arkansas 72703
Teva Investigational Site 052 Englewood Colorado 80113
Teva Investigational Site 333 Washington D.C. District of Columbia 20007
Teva Investigational Site 160 Gainesville Florida 32607
Teva Investigational Site 014 Miami Florida 33136
Teva Investigational Site 032 Atlanta Georgia 30329
Teva Investigational Site 045 Indianapolis Indiana 46202
Teva Investigational Site 024 Iowa City Iowa 52242
Teva Investigational Site 029 Kansas City Kansas 66160
Teva Investigational Site 083 Wichita Kansas 67226
Teva Investigational Site 087 Louisville Kentucky 40202
Teva Investigational Site 028 Baltimore Maryland 21287
Teva Investigational Site 040 Boston Massachusetts 02118
Teva Investigational Site 027 St Louis Missouri 63110
Teva Investigational Site 194 Las Vegas Nevada 89102
Teva Investigational Site 328 Camden New Jersey 08103
Teva Investigational Site 026 New Brunswick New Jersey 08901
Teva Investigational Site 037 Albany New York 12208
Teva Investigational Site 002 New York New York 10032
Teva Investigational Site 342 Patchogue New York 11772
Teva Investigational Site 119 Durham North Carolina 27705
Teva Investigational Site 089 Cincinnati Ohio 45267
Teva Investigational Site 020 Columbus Ohio 43210
Teva Investigational Site 093 Toledo Ohio 43614-2598
Teva Investigational Site 341 Tulsa Oklahoma 74136
Teva Investigational Site 031 Nashville Tennessee 37232-2551
Teva Investigational Site 007 Houston Texas 77030
Teva Investigational Site 199 Houston Texas 77030
Teva Investigational Site 100 Salt Lake City Utah 84108
Teva Investigational Site 137 Burlington Vermont 05401
Teva Investigational Site 220 Kirkland Washington 98034
Teva Investigational Site 096 Seattle Washington 98108

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01897896, 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 8, 2021 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01897896 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →