Status:
COMPLETED
Pivotal Efficacy and Safety Registration Trial of FP187 in Moderate to Severe Plaque Psoriasis
Lead Sponsor:
Forward-Pharma GmbH
Conditions:
Plaque Psoriasis
Eligibility:
All Genders
18-90 years
Phase:
PHASE2
Brief Summary
The purpose of this trial is to investigate the efficacy and safety of different doses and dose administrations of FP187 compared to a placebo treatment in patients with moderate to severe plaque psor...
Detailed Description
The trial tests two different dose levels and two different daily dosing schedules (twice daily (BID) and three times daily (TID))over 20 weeks of treatment. Key is effect as measured by achievement o...
Eligibility Criteria
Inclusion
- Patients of either sex at least 18 years of age
- A clinical diagnosis of plaque psoriasis defined as skin areas with erythema, induration and scaling, with a body surface area of no less than 10% and in total to be scoring at least 10 on the PASI scale
- The psoriasis disease have been stable for at least 6 months at randomization
- Signed and dated informed consent
- Sexually active females of childbearing potential must be either surgically sterile (hysterectomy or tubal ligation) or use a highly effective (failure rate \< 1%) medically accepted contraceptive method during the trial as well as one month after trial is finished such as:
- Systemic contraceptive (oral, implant, injection),
- Intrauterine device (IUD) inserted for at least one month prior to study entrance
- Willingness and ability to comply with the trial procedures
- Patient is beside the psoriasis disease in good general health in the opinion of the Investigator, as determined by medical history, physical examination, vital signs and clinical laboratory parameters (hematology, biochemistry and urinalysis).
Exclusion
- Female patients who are pregnant or breast-feeding or planning to become pregnant up to 7 months from treatment start as well as male patients plan-ning pregnancy with their partner up to 7 months from treatment start or practise unprotected sexual relationship up to 7 months from treatment start
- Known allergy to any of the constituents of the product being tested
- Pustular forms of psoriasis, erythrodermic or guttate psoriasis
- Known immunosuppressive diseases (e.g., AIDS/HIV)
- Presence of another serious or progressive disease which, according to the Investigator may interfere with treatment outcome
- Active skin disease such as atopic dermatitis, rosacea, lupus erythematosus, or other inflammatory or infectious skin disease which, according to the Investigator may interfere with treatment outcome
- Use of topical medical treatment or UVB treatment - Use of systemic anti-psoriatic treatment preceding the baseline visit Methotrexate, cyclosporine, steroids or PUVA treatment within x weeks; Biological treatment (efalizumab, adalimumab, infliximab, etanercept) within xx weeks; Acitretin within x months; Treatment with Fumaderm® or other DMF containing products during past xx weeks prior to baseline visit; Discontinuation of previous treatment with Fumaderm® or other DMF containing products due to lack of efficacy or side effects;
- Has within the past x weeks prior to baseline visit been treated with drugs influencing the course of the psoriasis such as antimalarial drugs, beta-blockers or lithium
- Has a relevant clinical history of stomach or intestinal problems (eg gastritis or peptic ulcer within the last 10 years )
- Has liver enzyme measures (AST, ALT, Gamma-GT) higher than 2x UNL)
- Has an estimated Creatinine Clearance: \< xx ml/min
- Has leucopenia (leukocyte count \< x/mm3) or eosinophilia (count \>x/µl) or lymphopenia (count \< x/nl).
- Has protein in the urine test at screening or baseline visit
- Participation in another clinical trial during the last month preceding the baseline visit or participation in a trial with treatment of biologicals within x months prior to baseline visit
- Patients who are involved in the organisation of the clinical investigation or are in any way dependant on the investigator or sponsor
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2012
Estimated Enrollment :
252 Patients enrolled
Trial Details
Trial ID
NCT01230138
Start Date
September 1 2010
End Date
May 1 2012
Last Update
December 11 2012
Active Locations (2)
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1
Dermatological Dept., Uniklinikum, TU-Dresden
Dresden, Germany, 01307
2
SCIderm
Hamburg, Germany, 20354