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Aprepitant – effect and safety in treatment of atopic dermatitis

Aprepitant – effect and safety in treatment of atopic dermatitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-002029-40-SE
Enrollment
50
Registered
2013-06-12
Start date
2013-08-23
Completion date
Unknown
Last updated
2020-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic Dermatitis

Interventions

Trade Name: Emend Product Name: Emend Pharmaceutical Form: Capsule, hard INN or Proposed INN: Emend CAS Number: 170729-80-3 Current Sponsor code: 1001 Other descriptive name: APREPITANT Concentration

Sponsors

Karolinska Institutet
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Ongoing atopic dermatitis (diagnosted by dermatologist, Williams criteria). - Moderate to severe disease (SCORAD > 20). - Local treatment have not given sufficient effect. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 50 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: - Age over 40 or under 20 years - Skin infection - Other sytemic treatment for the atopic dermatitis - Other diseases - Other regular medicial treatment (contraceptives not included here) - Dark skin (skin type VI)

Design outcomes

Primary

MeasureTime frame
Main Objective: To investigate the effect of Aprepitant (Emend) on atpoic dermatitis and prutitus.;Secondary Objective: To investigate inflammatory markers in the skin during treatment with Aprepitant (Emend). ;Primary end point(s): -7 (to 9) days of treatment.;Timepoint(s) of evaluation of this end point: - The day after end of treatment (day 8 in the trial)

Secondary

MeasureTime frame
Secondary end point(s): -moderate-severe side effects -patient wants to stop treatment;Timepoint(s) of evaluation of this end point: Day after end of treatment period.

Countries

Sweden

Contacts

Public ContactDep of dermatology, Karolinska Univ

Karolinska institutet

klas.nordlind@karolinska.se

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026