drugset / Trial / NCT03713957

A Study to Assess the Safety of GRF6021 Infusions in Subjects With Parkinson's Disease and Cognitive Impairment

NCT03713957 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the safety, tolerability, and potential effects on cognition of GRF6021, a plasma-derived product, administered as an intravenous (IV) infusion, to subjects with Parkinson's disease and cognitive impairment.

Timeline

Start
2018-11-12
Primary completion
2020-07-20
Completion
2020-07-20

Drugs

EvaluationDrugModalityDoseRoute
Subject GRF6021 Protein / enzyme biologic — Intravenous

Indications