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

Completed · Phase 3 · NCT04201093

Conditions: Parkinson Disease

At a glance

Research payments reported, 2025
$371,849
U.S. investigators named
30
Sites paid
31
Planned or actual enrollment
529

About the trial

Sponsor
AbbVie
Tested
Tavapadon (drug), Placebo (drug), Tavapadon (drug)
Dates
Started 2019-12-13; completion 2024-06-28
Results posted
Yes

The purpose of this study is to evaluate the clinical efficacy, safety and pharmacokinetics (PK) of 2 fixed doses of tavapadon and placebo in participants with early PD.

From ClinicalTrials.gov, last updated 2025-07-28. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $371,849 in research payments for this study in 2025 (71 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.