A Study to Investigate Efficacy and Safety With LEO 90100 Compared With Daivobet® Ointment in Adult Chinese Subjects With Stable Plaque Psoriasis

Prior treatment

• Systemic use of biological treatments with a potential effect on psoriasis vulgaris within the specified time periods prior to treatment assignment (depending on treatment)
• Systemic treatments with all therapies other than biological treatments with a potential effect on psoriasis vulgaris within 4 weeks prior to treatment assignment
• Psoralen combined with ultraviolet A therapy (PUVA) within 4 weeks prior to treatment assignment
• Systemic treatment with Apremilast within 4 weeks prior to treatment assignment
• Ultraviolet B (UVB) therapy within 2 weeks prior to treatment assignment
• Topical treatment of psoriasis with strong corticosteroids within 2 weeks prior to treatment assignment
• Topical treatment of psoriasis with traditional Chinese medicine within 2 weeks prior to treatment assignment
• Treatment with any non-marketed drug substance (any agent which has not yet been made available for clinical use) within 4 weeks/5 half-lives prior to treatment assignment
• Any other topical treatment that could affect plaque psoriasis within 2 weeks prior to treatment assignment
• Previously screened in this trial
• Participation in another clinical trial within 4 weeks prior to treatment assignment
• Chronic alcohol or drug abuse within 12 months prior to screening, or any condition associated with poor compliance

Other illness

• Patients with any of the following conditions present on any skin area: viral lesions, fungal and bacterial skin infections, parasitic infections, skin manifestations in relation to syphilis or tuberculosis, rosacea, acne vulgaris, acne rosacea, atrophic skin, striae atrophicae, fragility of skin veins, ichthyosis, ulcers and wounds
• Renal insufficiency, hepatic disorders or severe heart disease
• Cushing's disease or Addison's disease
• Known or suspected hypersensitivity to any component(s) of the investigational medicinal product (IMP)

Lab values

• Disorders of calcium metabolism

Other

• Current diagnosis of guttate, erythrodermic, exfoliative, pustular or unstable psoriasis
• Current participation in any other interventional clinical trial
• Women who are pregnant, wishing to become pregnant or are breast-feeding
• Employees of the trial site or any other individuals directly involved with the planning or conduct of the trial, or immediate family members of such individuals

• Chinese native
• Aged 18 or over
• A clinical diagnosis of stable plaque psoriasis for at least 6 months
• Stable plaque psoriasis on the trunk and/or limbs (excluding psoriasis on the face, scalp, genitals, and skin folds) involving 2-30% of the body surface at Day 1 (Visit 2) of the trial.
• Having a Physician Global Assessment of at least 'mild' at Day 1 (Visit 2)
• An mPASI score of at least 2 on the trunk and/or limbs at Day 1 (Visit 2)
• Women of childbearing potential must use an adequate form of birth control throughout the trial and for at least 8 weeks after last administration of IMP
• Male subjects with a female partner of childbearing potential must use adequate contraceptive methods (adequate contraceptive measures as required by local regulation or practice)
• Having a signed and dated informed consent.