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Not yet taking people in JapanPhase 3

Tests OPA-15406 foam against a vehicle in adults with atopic dermatitis

Tests OPA-15406 foam against a vehicle in adults with atopic dermatitis, a skin condition.

Plain-language title generated from the registry record
Registry title: A Phase 3 Trial to Demonstrate the Superiority of 1% OPA-15406 Foam to the Vehicle in Adult Patients With Atopic Dermatitis

Key facts

Where
Tokyo, JapanSee the site
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 15 and 70 years old?

Source: NCT07173478, who can take part

Where in Japan

  • Mita Dermatology ClinicTokyo, JapanNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Otsuka Pharmaceutical Co., Ltd.
Trial code
NCT07173478
Record updated
15 September 2025
Original description
To investigate the superiority of 1% OPA-15406 foam to the vehicle in adult patients with atopic dermatitis (AD).Read full original descriptionShow less

A Multicenter, Randomized, Double-blind, Vehicle-controlled, Parallel-group Comparison Trial to Demonstrate the Superiority of 1% OPA-15406 Foam to the Vehicle in Adult Patients With Atopic Dermatitis (Phase 3 Trial)

To investigate the superiority of 1% OPA-15406 foam to the vehicle in adult patients with atopic dermatitis (AD).

Inclusion: Participants who have been diagnosed AD based on the Diagnostic Criteria for Atopic Dermatitis (Criteria of the Japanese Dermatological Association); Participants with a history of AD for at least 3 years; Participants who have an affected area covering from 5% to 40% of their body surface area (excluding the scalp) at the screening and baseline examinations; Participants with an IGA score of 2 or 3 at the screening and baseline examinations.

Exclusion: Participants who experienced an acute exacerbation of AD or contact dermatitis within 28 days prior to the baseline examination; Participants who have been treated with OPA-15406 ointment in the past.

ClinicalTrials.gov NCT07173478