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

NCT03841331 · ClinicalTrials.gov registry record · Phase 2

Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Chronic Pruritus of Unknown Origin

A Phase 2 study, sponsored by Vyne Therapeutics.

Completed
Registry status
Phase 2
Development phase
233
Enrollment target

NCT03841331 is a Phase 2 study that has completed, run by Vyne Therapeutics. The registered enrollment target is 233 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03841331, a Phase 2 study, has completed, sponsored by Vyne Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
233 participants
Enrollment target

Study Summary

A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Chronic Pruritus of Unknown Origin

Interventions

  • DRUG 5 mg Serlopitant Tablets
  • DRUG Matching Placebo Tablets

Trial Details

FieldValue
Enrollment Target 233 participants
Start Date 2019-01-22
Est. Completion 2020-01-21
Phase Phase 2

Sponsor

Vyne Therapeutics

18 total trials

What the Registry Record Tells You About NCT03841331

The ClinicalTrials.gov registry entry for NCT03841331 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 233 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vyne Therapeutics, which has 18 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which 5 mg Serlopitant Tablets is the first listed.

NCT03841331 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03841331 about?

NCT03841331 is a clinical study titled "Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Chronic Pruritus of Unknown Origin". A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Chronic Pruritus of Unknown Origin

What is the current status of trial NCT03841331?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 233 participants. The study started on 2019-01-22. Estimated completion is 2020-01-21.

What interventions are being tested in trial NCT03841331?

The interventions under investigation include: 5 mg Serlopitant Tablets (DRUG), Matching Placebo Tablets (DRUG).

Who is sponsoring clinical trial NCT03841331?

This trial is sponsored by Vyne Therapeutics, which has 18 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.