Study of CRx-191 to Assess Activity in Plaque Psoriasis
Phase 2
Completed
- Conditions
- Plaque Psoriasis
- Interventions
- Registration Number
- NCT00557739
- Lead Sponsor
- Zalicus
- Brief Summary
CRx-191 is a proprietary synergistic combination drug candidate being evaluated by CombinatoRx for topical psoriasis therapy. CRx-191 was identified via a proprietary screening assay for novel drug combinations demonstrating enhanced inhibition of tumor necrosis factor- alpha and interferon-gamma release, cytokines that are implicated in the pathogenesis of psoriasis.
This clinical trial will assess the effectiveness of CRx-191 in reducing the psoriatic infiltrate band thickness as measured by transdermal ultrasound. All subjects will receive all treatments in separate test fields, with intra-individual comparison of the treatments.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Subject must voluntarily give written informed consent
- Subject must be between 18 and 70 years of age
- Subject must have chronic plaque psoriasis and stable plaques in an area sufficient for six treatment fields
- The physical examination must be without disease findings unless the investigator considers an abnormality to be irrelevant to the outcome of the study
- Sexually active females of childbearing potential should either be surgically sterile (hysterectomy or tubal ligation), or should use a highly effective medically accepted contraceptive regimen
Exclusion Criteria
- Erythrodermic, guttate or pustular psoriasis
- Cardiac disease, including recent myocardial infarction, any degree of heart block or other cardiac arrhythmias and valvular heart disease
- Mania
- Narrow angle glaucoma
- Hyperthyroidism by medical history, thyroid stimulating hormone (TSH) less than lower limit of normal (LLN), or receiving thyroid medication
- Intolerance to Lidocaine
- Severe liver disease (alanine aminotransferase (ALT) or aspartate aminotransferase (AST) laboratory values that exceed 1.5x upper limit of normal (ULN))
- Inflammatory dermatoses except psoriasis; bacterial, viral and fungal skin infections; facial rosacea
- Active varicella, tuberculosis, syphilis or post-vaccine reaction
- Autoimmune disease other than plaque psoriasis (e.g. lupus erythematosis and psoriatic arthritis)
- Known allergic reactions or hypersensitivity to any of the components of the study preparations
- Allergy to adhesives on the hydrocolloid dressing used in this study
- UV therapy in the four weeks before the study
- History of malignancy (except for treated or excised basal cell carcinoma)
- Surgery within the previous 3 months (except for minor cosmetic or dental procedures)
- History of drug or alcohol abuse (as defined by the Investigator)
- Symptoms of a clinically significant illness in the four weeks before the study that may influence the outcome of the study
- Positive for HIV antibody
- Subjects who require systemically acting medications for the treatment of psoriasis which might counter or influence the study objectives such as: Methotrexate; Cyclosporine; Anti-TNFα therapies
- Subjects who require medications that inhibit the CYP450 2D6 pathway such as: Quinidine; Cimetidine; Type 1 antiarrhythmics; Phenothiazines; Selective serotonin reuptake inhibitors such as fluoxetine, paroxetine, and sertraline; Reserpine, other anticholinergic drugs, and sympathomimetic drugs
- Topical treatments for psoriasis (except for salicylic acid in vaseline) in the four weeks preceding and during the study (topical corticosteroids disallowed for eight weeks prior to the study)
- Systemic treatments in the two weeks preceding and during the study that may interact with any of the study drugs, such as: Glucocorticoids (po, im, iv); MAO inhibitors; Anti-depressants; Anti-seizure medications; Anti-psychotics; Antihistamines
- Treatments in the two weeks preceding and during the study that may aggravate psoriasis, such as: Anti-malarials; Beta-blockers
- Participation in another clinical trial and/or treatment received with any investigational agent within one month before the initial dose of study medication
- Female subject who is pregnant or lactating
- Significant UV exposure in the four weeks before the study
- Unwilling or unable to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the subject's return for follow-up visits on schedule
- Other unspecified reasons that, in the opinion of the Investigator or sponsor make the subject unsuitable for enrollment
- Subject is institutionalized because of legal or regulatory order
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 nortriptyline HCl CRx-191 (0.1% mometasone furoate + 0.05% nortriptyline HCl) 6 Vehicle (placebo) Vehicle (placebo) 2 mometasone furoate CRx-191 (0.1% mometasone furoate + 0.1% nortriptyline HCl) 1 mometasone furoate CRx-191 (0.1% mometasone furoate + 0.05% nortriptyline HCl) 2 nortriptyline HCl CRx-191 (0.1% mometasone furoate + 0.1% nortriptyline HCl) 4 nortriptyline HCl 0.05% nortriptyline HCl 3 mometasone furoate 0.1% mometasone furoate 5 nortriptyline HCl 0.1% nortriptyline HCl
- Primary Outcome Measures
Name Time Method The primary efficacy endpoint is the difference in reduction from baseline in psoriatic infiltrate at Day 12 between CRx-191 and vehicle. Day 12
- Secondary Outcome Measures
Name Time Method Differences in reduction from baseline in psoriatic infiltrate at Day 12 between CRx-191 and its components, mometasone furoate and nortriptyline HCI. Demonstrate tolerability and safety of CRx-191. Day 12
Trial Locations
- Locations (1)
bioskin GmbH
🇩🇪Berlin, Germany