drugset / Trial / NCT03374917

A Study in Subjects With Parkinson's Disease to Evaluate the Safety and Tolerability of Titration and Continuous Subcutaneous Infusion of ABBV-951 in an Outpatient Environment

NCT03374917 ↗

Phase 1 Completed 20 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of 4 weeks of continuous infusion with ABBV-951 in adult subjects with Parkinson's Disease (PD).

Timeline

Start
2018-04-18
Primary completion
2019-03-04
Completion
2019-03-04

Drugs

EvaluationDrugModalityDoseRoute
Subject FOSLEVODOPA Small molecule — Subcutaneous

Indications