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
| Type | Name | Description |
|---|---|---|
| DRUG | TA-1790 | 2 TA-1790 100 mg capsules |
| DRUG | Sildenafil citrate | 2 sildenafil citrate 50 mg capsules |
| DRUG | Placebo | 2 placebo capsules for TA-1790 100 mg capsules |
| DRUG | Nitrostat | glyceryl 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.