LEO 43204 field treatment of AK on balding scalp

  • Research type

    Research Study

  • Full title

    Efficacy and Safety of LEO 43204 in Field Treatment of Actinic Keratosis on Balding Scalp including 12-month follow-up

  • IRAS ID

    193904

  • Contact name

    Mohammed Alif

  • Contact email

    mdaus@leo-pharma.com

  • Sponsor organisation

    LEO Pharma A/S

  • Eudract number

    2015-002451-10

  • Clinicaltrials.gov Identifier

    NCT02547363

  • Clinicaltrials.gov Identifier

    Derm 5004, NIHR CRN Study ID

  • Duration of Study in the UK

    1 years, 4 months, 9 days

  • Research summary

    Actinic keratosis (AK) is a common skin condition visible as thick, scaly, crusty patches of skin (called lesions or actinic keratoses). AKs develop on areas that are frequently exposed to the sun. Ingenol Mebutate, marketed as Picato® is a gel product applied to the skin to treat AKs in an area of up to 25cm2. LEO 43204 is a new form of ingenol being developed for treatment of AKs on a larger area, such as the full face, balding scalp or a large area on the chest (250 cm2). This trial will look at LEO 43204 gel 0.037% in the treatment of AKs on the balding scalp when applied for 3 consecutive days. AKs will be counted prior to treatment and at various points after treatment as a way of measuring how well the treatment works on reducing or clearing AKs in the treatment area. The emergence of new AKs in a defined area will also be recorded to gain some insight as to whether there is a reduction of newly emerging AKs after the treatment. Information on the safety of LEO 43204 gel will be collected as well as some information from the patients themselves. Patients with between 5 and 20 AKs within an area of 25 to 250cm2 on the balding scalp will be considered for this trial. Two thirds of the patients will receive LEO 43204 gel and one third will receive a vehicle (placebo). Participants will be followed for 14 months after receiving the treatment and will visit their research site ten times after the screening visit. The data in this trial will contribute to a phase III programme for this product, which may result in a novel treatment for AK over a large treatment area.

  • REC name

    West Midlands - Edgbaston Research Ethics Committee

  • REC reference

    15/WM/0410

  • Date of REC Opinion

    23 Dec 2015

  • REC opinion

    Further Information Favourable Opinion