A Study Evaluating Skin Irritation, Phototoxicity and Safety After Administration of LEO 90105 on Intact Skin of Healthy Japanese Male Subjects

LEO Pharma

Status and phase

Completed

Phase 1

Conditions

Healthy

Treatments

Drug: LEO 90105

Study type

Interventional

Funder types

Industry

Identifiers

NCT01293357

MCB 0901

Details and patient eligibility

About

The objective of the trial is to investigate skin irritation, phototoxicity and safety of LEO 90105 and its components by patchtest (48 hours closed patch test and photo patch test) in healthy Japanese male subjects.

Enrollment

20 patients

Sex

Male

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy Japanese male subjects,
Aged 20 to 40 years inclusive.
Subjects without signs of skin irritation (erythema,dryness, roughness or scaling) on test sites.
Subjects willing to follow the study procedures and complete the study Subjects having understood and signed a written informed consent.
Subjects without abnormal in physiological test and clinical test in screening, and also judged as possible to participant the study by investigators.

Exclusion criteria

Body mass Index (BMI ) (body weight (kg)/height(m)²) outside the range 18-25 kg/m2
History of alcohol, chemical or drug abuse
History of allergic reaction to drugs or history of skin reaction to the tape
Any systemic or cutaneous disease that could in any way confound interpretation of the study results (e.g. atopic dermatitis, eczema, psoriasis)
Known sensitivity to any component of any of the formulations being tested
Known hepatic or renal disorders
Use of systemic, locally injected or inhaled corticosteroids within 4 weeks of study start (Day 1)
Use of systemic vitamin D analogues, vitamin D or calcium supplements within 4 weeks of study start(Day 1)
Use of any drug (systemic or topical) within 2 weeks of study start (Day 1)
Use of non-marketed/other investigational products one month prior to or 5 half lives (for those the half life is longer than one month) and during the trial is not permitted
Any abnormality found at medical interview before administration of the test drug, which will affect the clinical study as judged by the investigator
History of or active photo-induced or photoaggravated disease (abnormal response to the sun light)
Exposure to excessive or chronic ultraviolet (UV)radiation (i.e., sunbathing, tanning salon use, phototherapy)within four weeks prior to inclusion (Day 1) or planned during the study period
Scars, moles, sunburn, or other blemishes in the test area which would interfere with grading
Subjects whose partner wishes to become pregnant but is unwilling to use birth control during the study
Any condition which, in the opinion of the investigator, would place the subject at an unacceptable risk if he participated in the study
Any disease which are contradictions for treatment of the investigation products or for which treatment with the investigation products needs to be carefully considered (Subjects with any of the following conditions present on the area(s) to be treated with study medication: viral (e.g., herpes or varicella) lesions of the skin, fungal or bacterial skin infections, parasitic infections, skin manifestations in relation to syphilis or tuberculosis, rosacea, acne vulgaris, atrophic skin, striae atrophicae, fragility of skin veins, ichthyosis, acne rosacea, ulcers or wounds).