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Completed Phase 2 Interventional Results available

Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Refractory Chronic Cough

ClinicalTrials.gov ID: NCT03282591

Public ClinicalTrials.gov record NCT03282591. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 27, 2026, 12:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Refractory Chronic Cough

Study identification

NCT ID
NCT03282591
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vyne Therapeutics Inc.
Industry
Enrollment
185 participants

Conditions and interventions

Interventions

  • 5 mg Serlopitant Tablets Drug
  • Matching Placebo Tablets Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2, 2017
Primary completion
Aug 14, 2018
Completion
Sep 5, 2018
Last update posted
May 19, 2021

2017 – 2018

United States locations

U.S. sites
29
U.S. states
14
U.S. cities
27
Facility City State ZIP Site status
Study Site 130 Los Angeles California 90048
Study Site 128 Mission Viejo California 92691
Study Site 123 San Diego California 92108
Study Site 127 San Jose California 95117
Study Site 131 Stockton California 95207
Study Site 106 Colorado Springs Colorado 80907
Study Site 113 Colorado Springs Colorado 80907
Study Site 108 Denver Colorado 80230
Study Site 118 Largo Florida 33778
Study Site 107 Winter Park Florida 32789
Study Site 115 Plymouth Minnesota 55441
Study Site 110 Rochester Minnesota 55905
Study Site 121 Ocean Township New Jersey 07712
Study Site 125 Rochester New York 14618
Study Site 129 Charleston North Carolina 29420
Study Site 103 Charlotte North Carolina 28207
Study Site 111 Gastonia North Carolina 28054
Study Site 114 Mooresville North Carolina 28117
Study Site 122 Cincinnati Ohio 45231
Study Site 112 Tulsa Oklahoma 74136
Study Site 117 Eugene Oregon 97401
Study Site 116 Portland Oregon 97202
Study Site 104 Rock Hill South Carolina 29732
Study Site 102 Dallas Texas 75231
Study Site 120 Dallas Texas 75231
Study Site 101 San Antonio Texas 78229
Study Site 109 Waco Texas 76712
Study Site 126 Bellingham Washington 98225
Study Site 105 Greenfield Wisconsin 53228

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03282591, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 19, 2021 · Synced Jun 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03282591 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →