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Effect of BIA 5-1058 on the Steady State Pharmacokinetics of Treprostinil

Pulmonary Arterial Hypertension Clinical Trial

Official title:
An Open-Label, Three Period, Fixed Sequence Study to Assess the Effect of a Single Dose of BIA 5 1058 200 mg on the Steady State Pharmacokinetics of Treprostinil in Healthy Subjects Under Fed Conditions

Clinical Trial Summary

The purpose of this study is to assess the effect of BIA 5-1058 200 mg on the pharmacokinetic (PK) of treprostinil

Clinical Trial Description

This study was an open-label, three period, fixed sequence study in healthy male and female subjects performed at a single study center. The study comprised: - Screening during Days -28 to -2 (both inclusive). - Three treatment periods separated by a washout period of at least 10 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04675944
Study type Interventional
Source Bial - Portela C S.A.
Contact
Status Completed
Phase Phase 1
Start date February 28, 2018
Completion date May 25, 2018
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