Trials / Completed
CompletedNCT00902512
Study Of Bioavailability Of Two Sildenafil 100mg Oral Tablet Formulations
Relative Bioavailability Of Two Sildenafil 100mg Oral Tablet Formulations In Healthy Volunteers Under Fasting Conditions.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
- Sex
- Male
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
the pharmacokinetics of sildenafil following single doses of sildenafil CT administered with and without water is similar relative to the conventional oral tablet of sildenafil administered with water.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Treatment A | Viagra® 100 mg tablet, administered with water single dose |
| DRUG | Blood samples for the analysis of sildenafil in plasma | Blood samples for the analysis of sildenafil in plasma |
| DRUG | Treatment B | Sildenafil 100 mg CT administered with water single dose |
| OTHER | Blood samples for the analysis of sildenafil in plasma | Blood samples for the analysis of sildenafil in plasma |
| DRUG | Treatment C | Sildenafil 100 mg CT administered without water single dose |
| OTHER | Blood samples for the analysis of sildenafil in plasma | Blood samples for the analysis of sildenafil in plasma |
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2009-04-01
- Completion
- 2009-04-01
- First posted
- 2009-05-15
- Last updated
- 2021-02-01
Locations
1 site across 1 country: Mexico
Source: ClinicalTrials.gov record NCT00902512. Inclusion in this directory is not an endorsement.