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NCT03781167 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Parkinson's Disease (PD)

A Phase 3 study, sponsored by AbbVie.

Completed
Registry status
Phase 3
Development phase
244
Enrollment target

NCT03781167 is a Phase 3 study that has completed, run by AbbVie. The registered enrollment target is 244 participants.

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The verdict

NCT03781167, a Phase 3 study, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 3
Development phase
244 participants
Enrollment target

Study Summary

The purpose of this study was to assess the safety and tolerability of ABBV-951 (Foslevodopa/Foscarbidopa) in participants with Parkinson's disease (PD). This was a single-arm study with preplanned analyses conducted by dose subgroup (Low Dose or High Dose) based on the modal total daily dose (most frequent dose) over the treatment period.

Interventions

  • DRUG ABBV-951

Trial Details

FieldValue
Enrollment Target 244 participants
Start Date 2019-04-29
Est. Completion 2022-08-17
Phase Phase 3

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT03781167

The ClinicalTrials.gov registry entry for NCT03781167 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 244 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which ABBV-951 is the first listed.

NCT03781167 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03781167 about?

NCT03781167 is a clinical study titled "A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Parkinson's Disease (PD)". The purpose of this study was to assess the safety and tolerability of ABBV-951 (Foslevodopa/Foscarbidopa) in participants with Parkinson's disease (PD). This was a single-arm study with preplanned analyses conducted by dose subgroup (Low Dose or High Dose) based on the modal total daily dose (most...

What is the current status of trial NCT03781167?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 244 participants. The study started on 2019-04-29. Estimated completion is 2022-08-17.

What interventions are being tested in trial NCT03781167?

The interventions under investigation include: ABBV-951 (DRUG).

Who is sponsoring clinical trial NCT03781167?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.