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Completed Phase 2 Interventional Results available

NBI-98854 Dose Titration Study for the Treatment of Tardive Dyskinesia

ClinicalTrials.gov ID: NCT01733121

Public ClinicalTrials.gov record NCT01733121. 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 Jul 22, 2026, 7:31 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

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Titration Study to Assess the Safety, Tolerability, and Efficacy of NBI-98854 for the Treatment of Tardive Dyskinesia

Study identification

NCT ID
NCT01733121
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

  • NBI-98854 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 85 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
Nov 30, 2012
Primary completion
Nov 30, 2013
Completion
Nov 30, 2013
Last update posted
Aug 9, 2017

2012 – 2013

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
20
Facility City State ZIP Site status
Not listed Costa Mesa California 92626
Not listed Fountain Valley California 92708
Not listed Oceanside California 92056
Not listed Englewood Colorado 80113
Not listed Boca Raton Florida 33486
Not listed Hialeah Florida 33012
Not listed Miami Florida 33125
Not listed Chicago Illinois 60640
Not listed Baltimore Maryland 21287
Not listed Farmington Hills Michigan 48334
Not listed Beachwood Ohio 44122
Not listed Middleburg Heights Ohio 44130
Not listed Conshohocken Pennsylvania 19428
Not listed Phoenixville Pennsylvania 19460
Not listed Bedford Texas 76021
Not listed DeSoto Texas 75115
Not listed Houston Texas 77008
Not listed Houston Texas 77030
Not listed Irving Texas 75062
Not listed San Antonio Texas 78229
Not listed Richland Washington 99352

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01733121, 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 Aug 9, 2017 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01733121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →