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NCT00458042 · ClinicalTrials.gov registry record · Phase 4
Transitioning To IV Remodulin From Ventavis in Patients With PAH: Safety, Efficacy and Treatment Satisfaction
A Phase 4 study, sponsored by United Therapeutics.
- Terminated
- Registry status
- Phase 4
- Development phase
- 10
- Enrollment target
NCT00458042: Clinical Trial Phase 4 study, sponsored by United Therapeutics.
NCT00458042 is a Phase 4 study that was terminated before completion, run by United Therapeutics. The registered enrollment target is 10 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00458042, a Phase 4 study, was terminated before completion, sponsored by United Therapeutics.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 10 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the effects of switching from inhaled Ventavis to intravenous Remodulin in PAH patients who are considered to be failing inhaled Ventavis therapy. This study is intended to provide information on the safe transition from Ventavis to Remodulin as well as the impact intravenous Remodulin may have on overall quality of life and treatment satisfaction compared to Ventavis.
Interventions
- DRUG treprostinil sodium
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2007-03 |
| Est. Completion | 2007-11 |
| Phase | Phase 4 |
Why NCT00458042 stopped before completion
NCT00458042 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 1 intervention - of which treprostinil sodium is the first listed.
NCT00458042 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00458042 about?
NCT00458042 is a clinical study titled "Transitioning To IV Remodulin From Ventavis in Patients With PAH: Safety, Efficacy and Treatment Satisfaction". The purpose of this study is to compare the effects of switching from inhaled Ventavis to intravenous Remodulin in PAH patients who are considered to be failing inhaled Ventavis therapy. This study is intended to provide information on the safe transition from Ventavis to Remodulin as well as the im...
What is the current status of trial NCT00458042?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 10 participants. The study started on 2007-03. Estimated completion is 2007-11.
What interventions are being tested in trial NCT00458042?
The interventions under investigation include: treprostinil sodium (DRUG).
Who is sponsoring clinical trial NCT00458042?
This trial is sponsored by United Therapeutics, which has 63 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00458042's enrollment target sits among peer trials
10 1940th of 2000 higher than 33 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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