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Completed Phase 3 Interventional Results available

Fixed-Dose Trial in Early Parkinson's Disease (PD)

ClinicalTrials.gov ID: NCT04201093

Public ClinicalTrials.gov record NCT04201093. 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 23, 2026, 4:17 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 3, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, 27-Week Trial to Evaluate the Efficacy, Safety, and Tolerability of Two Fixed Doses of Tavapadon in Early Parkinson's Disease (TEMPO-1 TRIAL)

Study identification

NCT ID
NCT04201093
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
529 participants

Conditions and interventions

Interventions

  • Tavapadon Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 80 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
Dec 12, 2019
Primary completion
Jun 27, 2024
Completion
Jun 27, 2024
Last update posted
Jul 27, 2025

2019 – 2024

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
27
Facility City State ZIP Site status
Birmingham, Alabama Birmingham Alabama 35233
Little Rock, Arkansas Little Rock Arkansas 72205
Fountain Valley, California Fountain Valley California 92708
Los Angeles, California Los Angeles California 90048
Pasadena, California Pasadena California 91105
Englewood, Colorado Englewood Colorado 80113
Adventura, Florida Adventura Florida 33180
Boca Raton, Florida Boca Raton Florida 33486
Tampa, Florida Tampa Florida 33613
Augusta, Georgia Augusta Georgia 30912
Savannah, Georgia Savannah Georgia 31406
Chicago, Illinois Chicago Illinois 60612
Kansas City, Kansas Kansas City Kansas 66160
Scarborough, Maine Scarborough Maine 04074
Boston, Massachusetts Boston Massachusetts 02215
East Lansing, Michigan East Lansing Michigan 48824
Las Vegas, Nevada Las Vegas Nevada 89106
Asheville, North Carolina Asheville North Carolina 28806
Durham, North Carolina Durham North Carolina 27705
Columbus, Ohio Columbus Ohio 43221
Toledo, Ohio Toledo Ohio 43614
Philadelphia, Pennsylvania Philadelphia Pennsylvania 19107
Georgetown, Texas Georgetown Texas 78628
Houston, Texas Houston Texas 77030
Lubbock, Texas Lubbock Texas 79410
Burlington, Vermont Burlington Vermont 05401
Virginia Beach, Virginia Virginia Beach Virginia 23456

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04201093, 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 Jul 27, 2025 · Synced Jul 23, 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 NCT04201093 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →