Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of TS-022 in Adult Patients With Atopic Dermatitis With Pruritus (POC)

ClinicalTrials.gov ID: NCT00914186

Public ClinicalTrials.gov record NCT00914186. 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 27, 2026, 1:46 PM 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 Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study of the Efficacy, Safety and Tolerability of TS-022 in Adult Patients With a Diagnosis of Atopic Dermatitis (AD) With Moderate to Very Severe Pruritus

Brief summary

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

The purpose and (primary) objectives of this study are to evaluate the efficacy, safety, and tolerability of TS-022 in adults with atopic dermatitis who have moderate to very severe pruritus (itching), following a 28-day regimen of twice-daily topical application.

Study identification

NCT ID
NCT00914186
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Taisho Pharmaceutical R&D Inc.
Industry
Enrollment
122 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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
Jun 2009 (Type not available)
Primary completion
May 2010 (Actual)
Completion
Oct 2010 (Actual)
Last update posted
Dec 1, 2011

2009 – 2010

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
UCSD La Jolla California 92037 —
Therapeutics Clinical Research San Diego California 92123 —
Ameriderm Research Jacksonville Florida 32216 —
Ameriderm Research Kissimmee Florida 34741 —
FXM Research Miramar Florida 33027 —
Ameriderm Research Ormond Beach Florida 32174 —
Gwinnett Clinical Research Snellville Georgia 30078 —
Minnesota Clinical Study Center Fridley Minnesota 55432 —
Comprehensive Clinical Research Berlin New Jersey 08009 —
Wake Forest University Winston-Salem North Carolina 27157 —
Haber Dermatology and Cosmetic Surgery, Inc South Euclid Ohio 44118 —
Oregon Health and Science University Portland Oregon 97239 —
J & S Studies College Station Texas 77845 —
Center for Clinical Studies Houston Texas 77030 —
Center for Clinical Studies Webster Texas 77598 —

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 NCT00914186, 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 Dec 1, 2011 · Synced Oct 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 public registry record, listed eligibility criteria, and available contact information for NCT00914186 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →