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

NCT04915950 · ClinicalTrials.gov registry record · Phase 2

A Study to Assess the Effect of Oral Temanogrel on Digital Blood Flow in Adult Participants With Raynaud's Phenomenon Secondary to Systemic Sclerosis

A Phase 2 study, sponsored by Pfizer.

Terminated
Registry status
Phase 2
Development phase
13
Enrollment target

NCT04915950 is a Phase 2 study that was terminated before completion, run by Pfizer. The registered enrollment target is 13 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04915950, a Phase 2 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 2
Development phase
13 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether oral temanogrel improves digital blood flow in participants with Raynaud's phenomenon secondary to systemic sclerosis (SSc-RP) as a potential safe and effective treatment for symptoms associated with SSc-RP.

Interventions

  • DRUG Placebo
  • DRUG Temanogrel

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2021-11-03
Est. Completion 2022-09-02
Phase Phase 2

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT04915950

The ClinicalTrials.gov registry entry for NCT04915950 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04915950 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04915950 about?

NCT04915950 is a clinical study titled "A Study to Assess the Effect of Oral Temanogrel on Digital Blood Flow in Adult Participants With Raynaud's Phenomenon Secondary to Systemic Sclerosis". The purpose of this study is to determine whether oral temanogrel improves digital blood flow in participants with Raynaud's phenomenon secondary to systemic sclerosis (SSc-RP) as a potential safe and effective treatment for symptoms associated with SSc-RP.

What is the current status of trial NCT04915950?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 13 participants. The study started on 2021-11-03. Estimated completion is 2022-09-02.

What interventions are being tested in trial NCT04915950?

The interventions under investigation include: Placebo (DRUG), Temanogrel (DRUG).

Who is sponsoring clinical trial NCT04915950?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

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

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.