Clinical Trials Directory

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

TypeNameDescription
DRUGTreatment AViagra® 100 mg tablet, administered with water single dose
DRUGBlood samples for the analysis of sildenafil in plasmaBlood samples for the analysis of sildenafil in plasma
DRUGTreatment BSildenafil 100 mg CT administered with water single dose
OTHERBlood samples for the analysis of sildenafil in plasmaBlood samples for the analysis of sildenafil in plasma
DRUGTreatment CSildenafil 100 mg CT administered without water single dose
OTHERBlood samples for the analysis of sildenafil in plasmaBlood 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.