Assessment of the Phototoxic Potential of LEO 29102 Cream

Inclusion Criteria: * Subjects having understood and signed an informed consent form * Male adults between the age of 18 and 65 years (both inclusive) * Healthy subjects without signs of skin irritation on test areas (erythema, dryness, roughness or scaling) * Subjects willing and able to follow all the study procedures and complete the whole study * Subjects affiliated to a social security system Exclusion Criteria: * Females * Males who are not willing to use a local contraception for the entire duration of the study, and refrain from fathering a child within 3 months following the study drug * Systemic treatments which may interfere with the inflammatory reaction (e.g., corticosteroids and other anti-inflammatory drugs) within 2 weeks prior to randomisation * Systemic or topical treatments suspected of causing photobiological reactions (e.g., tetracycline, thiazides, fluoroquinolones) within 4 weeks prior to randomisation * Exposure to excessive or chronic UV radiation (i.e., sunbathing, solarium, phototherapy) within 4 weeks prior to inclusion or is planned during the study period * Dark pigmentation of the skin or skin type that may, in any way, confound interpretation of the study results (skin types V and VI on the Fitzpatrick scale) * Scars, moles, sunburn or other blemishes in the test area which may interfere with grading * Any systemic or cutaneous disease on the test area that may confound interpretation of the study results (e.g., atopic dermatitis, eczema, psoriasis) * Relevant history of or concurrent photo-induced or photo-aggravated disease (abnormal response to sunlight * Subjects with a history of serious allergy, allergic skin rash or known sensitivity to any component of the investigational products * Subjects who have received treatment with any non-marketed drug substance (i.e., an agent which has not yet been made available for clinical use following registration) within the last four (4) weeks before randomisation * Participation in any other current interventional clinical trial based on interview of the subject * Previously randomised in this trial * Subjects impossible to contact in case of emergency * Subjects known or, in the opinion of the investigator, are unlikely to comply with the Clinical Study Protocol (e.g. alcoholism, drug dependency or psychotic state) * Subjects who are in an exclusion period in the National Biomedical Research Register of the French Ministry of Health * Subjects under guardianship, hospitalised in a public or private institution for a reason other than research or subject deprived of freedom