Clareo Health | A Proof of Concept Study Comparing Three Doses of an Oral Solution of LEO 22811 With a Placebo Oral Solution for the Treatment of Psoriasis Vulgaris
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
LEO Pharma
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Following verbal and written information about the trial the subject must provide signed and dated informed consent before any study related activity is carried out, including activities relating to the washout period.
Clinical diagnosis of psoriasis vulgaris, for at least 6 months prior to randomisation, and currently covering at least 10% of the body surface area (BSA)
Candidates for systemic anti-psoriatic treatment
Psoriasis Area and Severity Index (PASI) ≥10
Disease severity of moderate, severe or very severe according to the Investigators' Global Assessment of disease severity (IGA)
Aged 18 years or above
Any race or ethnicity
Males, surgically sterile females (bilateral tubal ligation, bilateral oophorectomy or hysterectomy) or post menopausal females (at least 1 year since last menses)
Attending hospital outpatient clinic or the private practice of a dermatologist
You may not be if
Systemic treatment with biological therapies whether marketed or not with a possible effect on psoriasis vulgaris within the following time periods prior to randomisation:
* Etanercept - 4 weeks
* Adalimumab, alefacept, infliximab - 2 months
* Ustekinumab - 4 months
Systemic treatment with all other therapies (other than biologics) with a possible effect on psoriasis vulgaris (e.g.corticosteroids, retinoids, immunosuppressants, methotrexate, cyclosporin or fumaric acid) within 4 weeks prior to randomisation
PUVA therapy within 4 weeks prior to randomisation
UVB therapy within 2 weeks prior to randomisation
Any topical treatment (except for emollients/ medicated shampoo) within 2 weeks prior to randomisation
Initiation of, or changes to concomitant medication that could affect psoriasis vulgaris (e.g. beta-blockers, anti-malaria drugs, lithium) 2 weeks prior to randomisation and during the study
Current diagnosis with erythrodermic, exfoliative or pustular psoriasis
Other current skin conditions that may confound the evaluation of psoriasis vulgaris as judged by the Investigator
Generally in good health and does not have any clinically significant cardiac, endocrinologic, pulmonary, neurologic, psychiatric, hepatic, renal, haematologic, or gastrointestinal disease, immunologic insufficiency, or other major diseases or current condition which, in the opinion of the Investigator, would put the subject at risk by participating in the study
Current active tuberculosis or latent tuberculosis
Planned exposure to the sun during the study that may affect psoriasis vulgaris
Known malignancy or history of malignancy (other than cervical carcinoma in situ, basal cell or squamous cell carcinoma) within the 5 year period prior to randomisation
Live vaccination within the 4 weeks prior to randomisation
Males who do not agree to use adequate contraception during the study (including follow-up) to ensure their partner does not become pregnant
Known or suspected hypersensitivity to component(s) of the investigational product
Current participation in any other interventional trial
Treatment with any non-marketed drug substance (i.e. an agent which has not yet been made available for clinical use following registration) within 4 weeks or 5 half-lives (whichever is longer) prior to randomisation
Previously randomised in this study
Known or, in the opinion of the Investigator, is unlikely to comply with the Clinical Study Protocol (e.g., alcohol abuse, drug dependency or psychotic state).
