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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT04223193

Public ClinicalTrials.gov record NCT04223193. 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 2, 2026, 7:04 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

A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Flexible-Dose, 27-Week Trial to Evaluate the Efficacy, Safety, and Tolerability of Tavapadon in Early Parkinson's Disease (TEMPO-2 Trial)

Brief summary

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

The purpose of this study is to assess the efficacy, safety, tolerability and pharmacokinetics (PK) of flexible doses of tavapadon in participants with Parkinson's Disease.

Study identification

NCT ID
NCT04223193
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
304 participants

Conditions and interventions

Interventions

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
Jan 5, 2020
Primary completion
Sep 30, 2024
Completion
Sep 30, 2024
Last update posted
Nov 20, 2025

2020 – 2024

United States locations

U.S. sites
18
U.S. states
9
U.S. cities
17
Facility City State ZIP Site status
Fresno, California Fresno California 93710
Boca Raton, Florida Boca Raton Florida 33487
Maitland, Florida Maitland Florida 32751
Ocala, Florida Ocala Florida 34470
Winter Park, Florida Winter Park Florida 32792
Boston Neuro Research Center North Dartmouth Massachusetts 02747
Albany, New York Albany New York 12208
Syracuse, New York Syracuse New York 13210
Cincinnati, Ohio Cincinnati Ohio 45212
Cleveland, Ohio Cleveland Ohio 44195
Memphis, Tennessee Memphis Tennessee 38157
Cypress, Texas Cypress Texas 77429
Houston, Texas Houston Texas 77030
Lubbock, Texas Lubbock Texas 79410
Round Rock, Texas Round Rock Texas 78681
Richmond, Virginia Richmond Virginia 23229
Richmond, Virginia Richmond Virginia 23233
Kirkland, Washington Kirkland Washington 98034

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 NCT04223193, 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 20, 2025 · Synced Sep 2, 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 NCT04223193 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →