Phase 3
N=604
A Study to Investigate Efficacy and Safety With LEO 90100 Compared With Daivobet® Ointment in Adult Chinese Subjects With Stable Plaque Psoriasis
Stable Plaque Psoriasis
Bottom Line
View on ClinicalTrials.gov: NCT05919082 ↗Enrolled (actual)
604
Serious AEs
0.7%
Results posted
Mar 2025
Primary outcome: Primary: Percentage of Participants With Physician's Global Assessment of Disease Severity (PGA) Score of 0 (Clear) or 1 (Almost Clear) at Day 29, With at Least a 2-point Reduction From Baseline — 50.0; 42.4 Percentage of Participants — p=0.0438
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- LEO 90100 (Drug); Daivobet® ointment (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- LEO Pharma
- Primary completion
- Feb 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Participants With Physician's Global Assessment of Disease Severity (PGA) Score of 0 (Clear) or 1 (Almost Clear) at Day 29, With at Least a 2-point Reduction From Baseline |
50.0; 42.4 | 0.0438 sig |
| SECONDARY Percentage of Participants With Decrease in Modified Psoriasis Area and Severity Index of at Least 75% (mPASI-75) From Baseline to Day 29 |
63.6; 53.6 | 0.0108 sig |
| SECONDARY Percentage of Participants With Decrease in mPASI of at Least 90% (mPASI-90) From Baseline to Day 29 |
33.1; 24.5 | 0.0199 sig |
| SECONDARY Number of Participants With Treatment-emergent Adverse Events (TEAEs) |
77; 68; 0; 0; 4; 0 | — |
Summary
This study is conducted to assess the efficacy and safety of LEO 90100 when used on the body for the treatment of stable plaque psoriasis in native adult Chinese subjects, compared to Daivobet® ointment.
Eligibility Criteria
Inclusion Criteria
- 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.
Exclusion Criteria
- 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
- Current diagnosis of guttate, erythrodermic, exfoliative, pustular or unstable psoriasis
- 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
- Disorders of calcium metabolism
- 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)
- Current participation in any other interventional clinical trial
- Previously screened in this trial
- Participation in another clinical trial within 4 weeks prior to treatment assignment
- Women who are pregnant, wishing to become pregnant or are breast-feeding
- Chronic alcohol or drug abuse within 12 months prior to screening, or any condition associated with poor compliance
- 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
Data sourced from ClinicalTrials.gov (NCT05919082). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.