Clinical Trials Directory

Trials / Completed

CompletedNCT04994860

Effect of BIA 5-1058 400 mg on the Steady State Pharmacokinetics of Sildenafil

An Open-Label, Three Period, Fixed Sequence Study to Assess the Effect of a Single Dose of BIA 5-1058 400 mg on the Steady State Pharmacokinetics of Sildenafil in Healthy Subjects Under Fasting Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Bial - Portela C S.A. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is: * To assess the effect of BIA 5 1058 400 mg on the pharmacokinetics (PK) of sildenafil. * To assess the effect of sildenafil on the PK of BIA 5-1058.

Detailed description

This study was an open label, three period, fixed sequence study in healthy male and female subjects performed under fasting conditions 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. Duration of Treatment: The duration of participation for each subject was approximately 2 months and 3 weeks (including the screening period).

Conditions

Interventions

TypeNameDescription
DRUGBIA 5-1058Oral BIA 5-1058 (Zamicastat) 100 mg tablets
DRUGSildenafilOral Sildenafil ( Revatio) 20 mg film coated tablets

Timeline

Start date
2018-03-22
Primary completion
2018-06-07
Completion
2018-06-07
First posted
2021-08-06
Last updated
2021-08-06

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04994860. Inclusion in this directory is not an endorsement.