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NCT03033498 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous Infusions of ABBV-951 in Subjects With Parkinson's Disease

A Phase 1 study of Parkinsons Disease (PD), sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
29
Enrollment target
7
Study locations

NCT03033498 is a Phase 1 study of Parkinsons Disease (PD) that has completed, run by AbbVie. The registered enrollment target is 29 participants, below the 118-participant average among 19 other Parkinsons Disease (PD) trials with a reported enrollment target (75% lower). The trial reports 7 study locations across 7 states.

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The verdict

NCT03033498, a Phase 1 study of Parkinsons Disease (PD), has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
29 participants
Enrollment target
7
Study locations

Study Summary

The purpose of the study is to assess the safety, tolerability, and pharmacokinetics of single, ascending doses of ABBV-951 administered as a subcutaneous bolus infusion followed by a continuous subcutaneous infusion in subjects with Parkinson's disease.

Conditions Studied

Interventions

  • DRUG ABBV-951

Study Locations (7)

California

  • Glendale Adventist Medical Ctr /ID# 166512 - Glendale

Florida

  • Bioclinica Research - Orlando /ID# 169687 - Orlando

Illinois

  • Acpru /Id# 154976 - Grayslake

Kentucky

  • University of Kentucky Chandler Medical Center /ID# 169086 - Lexington

Maryland

  • Parexel Baltimore /ID# 169255 - Baltimore

Michigan

  • QUEST Research Institute /ID# 166035 - Farmington Hills

North Carolina

  • Carolina Phase I, LLC /ID# 166034 - Raleigh

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2017-05-17
Est. Completion 2019-06-08
Phase Phase 1

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT03033498

The ClinicalTrials.gov registry entry for NCT03033498 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 118-participant average among 19 other Parkinsons Disease (PD) trials with a reported enrollment target (75% lower). The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Parkinsons Disease (PD) appearing as the primary indexed condition, and to 1 intervention - of which ABBV-951 is the first listed.

NCT03033498 reports 7 study locations spanning 7 distinct geographic areas - top geographies include California, Florida, Illinois.

Frequently Asked Questions

What is clinical trial NCT03033498 about?

NCT03033498 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous Infusions of ABBV-951 in Subjects With Parkinson's Disease". The purpose of the study is to assess the safety, tolerability, and pharmacokinetics of single, ascending doses of ABBV-951 administered as a subcutaneous bolus infusion followed by a continuous subcutaneous infusion in subjects with Parkinson's disease.

What is the current status of trial NCT03033498?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2017-05-17. Estimated completion is 2019-06-08.

What conditions does trial NCT03033498 study?

This clinical trial studies the following conditions: Parkinsons Disease (PD).

What interventions are being tested in trial NCT03033498?

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

Who is sponsoring clinical trial NCT03033498?

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

Where is trial NCT03033498 being conducted?

This trial has 7 study locations across California, Florida, Illinois, Kentucky, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.