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Trial NCT00707070

Resource URI: http://data.linkedct.org/resource/trials/NCT00707070
PropertyValue
linkedct:acronym CobAcE
linkedct:arm_group <http://data.linkedct.org/resource/arm_group/16629>
linkedct:arm_group <http://data.linkedct.org/resource/arm_group/3945>
linkedct:brief_title Combining Acitretin and Efalizumab in the Therapy of Chronic Plaque Psoriasis
linkedct:condition <http://data.linkedct.org/resource/condition/2837>
linkedct:criteria Inclusion Criteria: - Men aged 18-70 - Women in postmenopausal - Moderate to severe chronic plaque psoriasis in patients with contraindication, intolerance or non responsive to cyclosporine, methotrexate or PUVA - PASI > 10 e/o BSA (Body Surface Area) > 10 Exclusion Criteria: - Drug induced psoriasis - Pustular or erythrodermic psoriasis - Fertile women - Pregnancy or lactation - cholesterol > 230mg/dL e triglyceride > 200 mg/dL - Known intolerance to efalizumab and acitretin - Serious infection at enrollement - History of previous neoplasia
linkedct:download_date Information obtained from ClinicalTrials.gov on December 30, 2009
linkedct:eligibility_gender Both
linkedct:eligibility_healthy_volunteers Accepts Healthy Volunteers
linkedct:eligibility_maximum_age 70 Years
linkedct:eligibility_minimum_age 18 Years
linkedct:end_date October 2009
linkedct:enrollment 100 (xsd:int)
linkedct:firstreceived_date June 26, 2008
linkedct:has_dmc No
linkedct:id NCT00707070
linkedct:intervention <http://data.linkedct.org/resource/intervention/22290>
linkedct:intervention <http://data.linkedct.org/resource/intervention/22310>
rdfs:label Trial NCT00707070
linkedct:lastchanged_date June 27, 2008
linkedct:lead_sponsor_agency <http://data.linkedct.org/resource/agency/2845>
linkedct:location <http://data.linkedct.org/resource/location/80178>
linkedct:nct_id NCT00707070
linkedct:number_of_arms 2 (xsd:int)
linkedct:number_of_groups 0 (xsd:int)
linkedct:official_title Phase IV Study on Efficacy and Safety of the Combination Treatment Acitretin and Efalizumab in Moderate to Severe Chronic Plaque Psoriasis
linkedct:org_study_id Gisondi 2
linkedct:overall_contact_email giampiero.girolomoni@univr.it
linkedct:overall_contact_last_name Giampiero Girolomoni, Prof
linkedct:overall_contact_phone 39-045-812-2547
linkedct:overall_contact_phone_ext 0039
linkedct:overall_official <http://data.linkedct.org/resource/overall_official/20030>
linkedct:overall_status Not yet recruiting
linkedct:oversight <http://data.linkedct.org/resource/oversight/1550>
foaf:page <http://clinicaltrials.gov/show/NCT00707070>
linkedct:phase Phase 4
linkedct:primary_completion_date October 2009
linkedct:primary_outcomes <http://data.linkedct.org/resource/primary_outcomes/77112>
linkedct:reference <http://data.linkedct.org/resource/reference/35653>
linkedct:secondary_id No grants were received
linkedct:secondary_outcomes <http://data.linkedct.org/resource/secondary_outcomes/105975>
linkedct:source Universita di Verona
linkedct:start_date September 2008
linkedct:study_design Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study
linkedct:study_type Interventional
linkedct:summary It is a phase IV multicentric, placebo-controlled, clinical trial investigating the efficacy and safety of acitretin combined to efalizumab in the therapy of chronic plaque psoriasis. PASI 75 at week 24 will be the primary end point. PASI 75 at week 12, and PASI 50 at week 24 will be the secondary end points. Safety measures will be the monitoring of serum parameters including AST; ALT; gammaGT; creatinine; cholesterol and triglycerides.
rdf:type linkedct:trials
linkedct:verification_date June 2008