drugset / Trial / NCT02772627

Study to Investigate the Tolerability, Steady-state Pharmacokinetics and Erythrocyte COMT Inhibition of BIA 3-202

NCT02772627

Phase 1 Completed 22 enrolled Bial - Portela C S.A.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate the tolerability and safety of three multiple dose regimens of nebicapone (BIA 3-202 100 mg, 200 mg, and 300 mg 6 times daily) in healthy volunteers. To characterise the steady-state pharmacokinetic and erythrocyte COMT inhibition profiles of nebicapone in healthy volunteers.

Timeline

Start
2001-09
Primary completion
2001-12
Completion
2001-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Nebicapone Small molecule 100 mg Oral
Subject Nebicapone Small molecule 200 mg Oral
Subject Nebicapone Small molecule 300 mg Oral

Indications