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Completed Phase 2 Interventional Results available

Study of the Efficacy, Safety, and Tolerability of Serlopitant for Pruritus (Itch) in Atopic Dermatitis

ClinicalTrials.gov ID: NCT02975206

Public ClinicalTrials.gov record NCT02975206. 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 Oct 26, 2026, 8:27 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 Pruritus In Adults And Adolescents With A History Of Atopic Dermatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Study of the Efficacy, Safety, and Tolerability of Serlopitant for Pruritus (Itch) in Atopic Dermatitis

Study identification

NCT ID
NCT02975206
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vyne Therapeutics Inc.
Industry
Enrollment
484 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 Years and older
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
Nov 2016 (Actual)
Primary completion
Jan 16, 2018 (Actual)
Completion
Feb 23, 2018 (Actual)
Last update posted
May 20, 2021

2016 – 2018

United States locations

U.S. sites
52
U.S. states
23
U.S. cities
47
Facility City State ZIP Site status
Study Site 332 Anniston Alabama — —
Study Site 363 Birmingham Alabama — —
Study Site 340 Hoover Alabama — —
Study Site 364 Glendale Arizona — —
Study Site 334 Cerritos California — —
Study Site 386 Encinitas California — —
Study Site 366 Fountain Valley California — —
Study Site 338 Los Angeles California — —
Study Site 383 North Hollywood California — —
Study Site 374 Oceanside California — —
Study Site 347 San Diego California — —
Study Site 356 San Diego California — —
Study Site 333 San Francisco California — —
Study Site 376 Santa Monica California — —
Study Site 358 Denver Colorado — —
Study Site 370 Jacksonville Florida — —
Study Site 331 Miami Florida — —
Study Site 348 Miami Florida — —
Study Site 378 Miami Florida — —
Study Site 353 Pinellas Park Florida — —
Study Site 368 Tampa Florida — —
Study Site 377 Tampa Florida — —
Study Site 369 Atlanta Georgia — —
Study Site 349 Savannah Georgia — —
Study Site 381 Chicago Illinois — —
Study Site 360 New Albany Indiana — —
Study Site 380 Bardstown Kentucky — —
Study Site 344 Louisville Kentucky — —
Study Site 379 Boston Massachusetts — —
Study Site 350 Warren Michigan — —
Study Site 371 Saint Joseph Missouri — —
Study Site 387 Las Vegas Nevada — —
Study Site 352 Berlin New Jersey — —
Study Site 375 Forest Hills New York — —
Study Site 373 Rochester New York — —
Study Site 341 High Point North Carolina — —
Study Site 355 Shelby North Carolina — —
Study Site 337 Oklahoma City Oklahoma — —
Study Site 345 Johnston Rhode Island — —
Study Site 362 Providence Rhode Island — —
Study Site 382 Anderson South Carolina — —
Study Site 343 Spartanburg South Carolina — —
Study Site 357 Chattanooga Tennessee — —
Study Site 365 Austin Texas — —
Study Site 335 Houston Texas — —
Study Site 359 Pflugerville Texas — —
Study Site 339 Plano Texas — —
Study Site 361 San Antonio Texas — —
Study Site 351 Draper Utah — —
Study Site 342 Norfolk Virginia — —
Study Site 336 Richmond Virginia — —
Study Site 367 Richmond Virginia — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02975206, 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 20, 2021 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02975206 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →