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OpenTrials
Completed

NCT Number: NCT02664805

Proof of Concept, Twice Daily Applications of LEO 124249 Ointment in the Treatment of Chronic Hand Eczema

To compare the efficacy of twice daily applications of LEO 124249 ointment with LEO 124249 ointment vehicle for up to 8 weeks in the treatment of subjects with chronic hand eczema.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Allergie-Centrum-Charité Klinik für Dermatologie, Venerologie und Allergologie

Berlin, 10117, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of chronic hand eczema with or without atopic etiology/background with a history of not adequately controlled disease activity with cutaneously applied steroid
  • Physician's Global Assessment of disease severity graded as at least mild at Visit 1
  • In overall good health including well controlled diseases

Exclusion criteria

  • Systemic treatment with immunosuppressive drugs (e.g. methotrexate, cyclosporine, azathioprine), retinoids (e.g. alitretinoin) or corticosteroids within 6 weeks prior to randomization (inhaled or intra-nasal steroids corresponding to up to 1 mg prednisone for asthma or rhinitis may be used).
  • PUVA (Psoralen Ultraviolet A) or UVB (Ultraviolet B) therapy on the hands within 4 weeks prior to randomization
  • Cutaneously applied treatment with immunomodulators (pimecrolimus, tacrolimus) or corticosteroids on the hands within 2 weeks prior to randomization.
  • Use of systemic antibiotics or cutaneously applied antibiotics on the hands within 2 weeks prior to randomization
  • Concurrent skin diseases on the hands
  • Current diagnosis of exfoliative dermatitis
  • Significant clinical infection (impetiginized hand eczema) on the hands which requires antibiotic treatment
  • A marked abnormal ECG at baseline
  • Known hepatic dysfunction or hepatic dysfunction tested at Screening
  • Current participation in any other interventional clinical trial

Treatment and study plan

LEO 124249 ointment

Drug

Ointment

LEO 124249 ointment vehicle

Drug

Ointment vehicle

Primary outcomes

  1. Subjects with treatment success according to Physician's Global Assessment (PGA) at visit 6 (End of Treatment)

    Time frame: 56 days

    Treatment success according to the PGA is defined as: Subjects having mild disease at baseline must achieve clear. Subjects having moderate or severe disease at baseline must achieve clear or almost clear

Secondary outcomes

  1. Hand Eczema Severity Index (HECSI) at visit 6

    Time frame: 56 days

  2. Subjects with treatment success according to the Patient's Global Assessment of disease severity (PaGA) at visit 6 (End of Treatment)

    Time frame: 56 days

    Treatment success according to the PaGA is defined as: Subjects having very mild or mild disease at baseline must achieve clear. Subjects having moderate or severe disease at baseline must achieve clear or very mild

Sponsors and collaborators

Lead sponsor

LEO Pharma

Industry

Registry information

Official study title

A Phase 2a, Proof of Concept Trial, Testing Twice Daily Applications of LEO 124249 Ointment in the Treatment of Chronic Hand Eczema

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Jan 27, 2016
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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