Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00159861 · ClinicalTrials.gov registry record · Phase 3

The Efficacy and Safety of Sildenafil Citrate Used in Combination With Intravenous Epoprostenol in PAH

A Phase 3 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

Completed
Registry status
Phase 3
Development phase
267
Enrollment target

NCT00159861 is a Phase 3 study that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 267 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00159861, a Phase 3 study, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

COMPLETED
Registry status
Phase 3
Development phase
267 participants
Enrollment target

Study Summary

Determination of the effects of sildenafil citrate and epoprostenol when used in combination in patients with pulmonary arterial hypertension

Interventions

  • DRUG Sildenafil citrate

Trial Details

FieldValue
Enrollment Target 267 participants
Start Date 2003-07
Est. Completion 2006-01
Phase Phase 3

What the Registry Record Tells You About NCT00159861

The ClinicalTrials.gov registry entry for NCT00159861 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 267 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Sildenafil citrate is the first listed.

NCT00159861 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00159861 about?

NCT00159861 is a clinical study titled "The Efficacy and Safety of Sildenafil Citrate Used in Combination With Intravenous Epoprostenol in PAH". Determination of the effects of sildenafil citrate and epoprostenol when used in combination in patients with pulmonary arterial hypertension

What is the current status of trial NCT00159861?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 267 participants. The study started on 2003-07. Estimated completion is 2006-01.

What interventions are being tested in trial NCT00159861?

The interventions under investigation include: Sildenafil citrate (DRUG).

Who is sponsoring clinical trial NCT00159861?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.