Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00914186 · ClinicalTrials.gov registry record · Phase 2
Study of TS-022 in Adult Patients With Atopic Dermatitis With Pruritus (POC)
A Phase 2 study, sponsored by Taisho Pharmaceutical R&D.
- Completed
- Registry status
- Phase 2
- Development phase
- 122
- Enrollment target
NCT00914186: Completed Phase 2 study, sponsored by Taisho Pharmaceutical R&D.
NCT00914186 is a Phase 2 study that has completed, run by Taisho Pharmaceutical R&D. The registered enrollment target is 122 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00914186, a Phase 2 study, has completed, sponsored by Taisho Pharmaceutical R&D.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 122 participants
- Enrollment target
Study Summary
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.
Primary Outcome
Patient reported outcome of pruritis measurement (0-100 mm/min-max)on a change in visual analog scale
Interventions
- DRUG Vehicle
- DRUG TS022
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 122 participants |
| Start Date | 2009-06 |
| Est. Completion | 2010-10 |
| Phase | Phase 2 |
What the finished NCT00914186 record still lists
NCT00914186 is an interventional study that assigns participants to a tested intervention. The registered 122 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Vehicle is the first listed.
NCT00914186 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00914186 about?
NCT00914186 is a clinical study titled "Study of TS-022 in Adult Patients With Atopic Dermatitis With Pruritus (POC)". 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.
What is the current status of trial NCT00914186?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 122 participants. The study started on 2009-06. Estimated completion is 2010-10.
What interventions are being tested in trial NCT00914186?
The interventions under investigation include: Vehicle (DRUG), TS022 (DRUG).
Who is sponsoring clinical trial NCT00914186?
This trial is sponsored by Taisho Pharmaceutical R&D, which has 8 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00914186's enrollment target sits among peer trials
122 565th of 2000 higher than 1,434 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03363373 · 122 participants · Phase 2
Naxitamab for High-Risk Neuroblastoma Patients With Primary Refractory Disease or Incomplete Response to Salvage Treatment in Bone and/or Bone Marrow
- NCT03463954 · 122 participants · NA
Confirmatory Clinical Evaluation of Novilase® Laser Therapy for Focal Destruction of Malignant Breast Tumors
- NCT04503265 · 122 participants · Phase 1
A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies
- NCT04700527 · 122 participants · Phase 1
The Effects of SCFA Supplementation in Subjects Receiving Abdominopelvic RT: A Randomized Controlled Study
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia