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NCT04955990 · ClinicalTrials.gov registry record · Phase 4

A Study of Real-world Cohort of Pulmonary Arterial Hypertension (PAH) Participants

A Phase 4 study, sponsored by Actelion.

Terminated
Registry status
Phase 4
Development phase
232
Enrollment target

NCT04955990: Clinical Trial Phase 4 study, sponsored by Actelion.

NCT04955990 is a Phase 4 study that was terminated before completion, run by Actelion. The registered enrollment target is 232 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04955990, a Phase 4 study, was terminated before completion, sponsored by Actelion.

TERMINATED
Registry status
Phase 4
Development phase
232 participants
Enrollment target

Study Summary

This study is designed to describe pulmonary arterial hypertension (PAH) participants in terms of their clinical characteristics, therapies used, disease progression, and outcomes (example, death, hospitalization, risk category for predicted mortality risk, and patient-reported outcomes \[PROs\]) in real-world clinical practice. This study will collect high-quality real-world data that may be used as a stand-alone dataset or in combination with other studies to address relevant research questions (example, serve as an external control dataset to another study) to support development and access to PAH therapies, as well as to contribute to the knowledge base of PAH through publications.

Primary Outcome

Time to all cause death will be reported. All-cause death defined as deaths due to any cause.

Interventions

  • OTHER PAH Therapies

Trial Details

FieldValue
Enrollment Target 232 participants
Start Date 2021-10-14
Est. Completion 2022-12-20
Phase Phase 4
Actelion

63 total trials

Why NCT04955990 stopped before completion

NCT04955990 is an interventional study that assigns participants to a tested intervention. The registered 232 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (55% lower).

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

NCT04955990 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04955990 about?

NCT04955990 is a clinical study titled "A Study of Real-world Cohort of Pulmonary Arterial Hypertension (PAH) Participants". This study is designed to describe pulmonary arterial hypertension (PAH) participants in terms of their clinical characteristics, therapies used, disease progression, and outcomes (example, death, hospitalization, risk category for predicted mortality risk, and patient-reported outcomes \[PROs\]) in...

What is the current status of trial NCT04955990?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 232 participants. The study started on 2021-10-14. Estimated completion is 2022-12-20.

What interventions are being tested in trial NCT04955990?

The interventions under investigation include: PAH Therapies (OTHER).

Who is sponsoring clinical trial NCT04955990?

This trial is sponsored by Actelion, which has 63 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04955990's enrollment target sits among peer trials

232 370th of 2000 higher than 1,631 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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Source: ClinicalTrials.gov NCT04955990, the US trial registry maintained by the National Library of Medicine. NCT04955990 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.