drugset / Trial / NCT03033498

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

NCT03033498 ↗

Phase 1 Completed 29 enrolled AbbVie
RandomizedParallel-groupSingle-blindTreatment

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.

Timeline

Start
2017-05-17
Primary completion
2019-06-08
Completion
2019-06-08

Drugs

EvaluationDrugModalityDoseRoute
Subject FOSLEVODOPA Small molecule — Subcutaneous

Indications