drugset / Trial / NCT02847442

Efficacy and Safety of Opicapone in Clinical Practice

NCT02847442

Phase 4 Completed 518 enrolled Bial - Portela C S.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the change in subject's condition according to the Investigator's Global Assessment of Change after three months of treatment with 50 mg opicapone once daily in a heterogeneous patient population reflecting daily clinical practice.

Timeline

Start
2016-11-23
Primary completion
2018-07-04
Completion
2018-07-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Opicapone Small molecule 50 mg Oral

Indications