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
| Type | Name | Description |
|---|---|---|
| DRUG | BIA 5-1058 | Oral BIA 5-1058 (Zamicastat) 100 mg tablets |
| DRUG | Sildenafil | Oral 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.