Clinical Trials Directory

Trials / Completed

CompletedNCT01616485

Study to Evaluate Hemodynamic Response to to a Sublingual Dose of Glyceryl Trinitrate in Subjects Receiving TA-1790, Sildenafil Citrate, and Placebo

A Double-blind, Randomized, Crossover Evaluation of the Hemodynamic Response to Sublingual Glyceryl Trinitrate in Patients Receiving TA-1790, Sildenafil, and Placebo

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
106 (actual)
Sponsor
VIVUS LLC · Industry
Sex
Male
Age
30 Years – 60 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to evaluate the hemodynamic response to a sublingual dose of glyceryl trinitrate in subjects receiving oral TA-1790, sildenafil citrate, and placebo.

Conditions

Interventions

TypeNameDescription
DRUGTA-17902 TA-1790 100 mg capsules
DRUGSildenafil citrate2 sildenafil citrate 50 mg capsules
DRUGPlacebo2 placebo capsules for TA-1790 100 mg capsules
DRUGNitrostatglyceryl trinitrate tablet, USP 0.4 mg

Timeline

Start date
2004-03-01
Primary completion
2004-05-01
Completion
2004-05-01
First posted
2012-06-11
Last updated
2012-06-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01616485. Inclusion in this directory is not an endorsement.

Study to Evaluate Hemodynamic Response to to a Sublingual Dose of Glyceryl Trinitrate in Subjects Receiving TA-1790, Sil (NCT01616485) · Clinical Trials Directory