Documentation of Humira in Psoriasis Patients in Routine Clinical Practice

Study Identifier
P10-446
CT.gov Identifier
NCT01077232
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Scientific Result Summary
Available Language(s): English
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Study Details

Medical Condition
  • Dermatology - Psoriasis (PsO)
    • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    18 - 99 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    \- Moderate to severe plaque psoriasis in adults with no response to other systemic therapy (e.g. cyclosporine, methotrexate or PUVA (photochemical therapy)) or patients with a contraindication or hypersensitivity to such a therapy
    Exclusion Criteria:
    \- Hypersensitivity against the drug or one of the other ingredients; active tuberculosis or other severe infections (e.g. sepsis and opportunistic infections); moderate to severe cardiac insufficiency

    Protocol Summary

    Safety and Effectiveness of adalimumab (Humira) in Psoriasis Patients in Routine Clinical Practice.

    Study Locations

    Location
    Status
    Location
    Universitaetsklinik Heidelberg /ID# 33810
    Heidelberg, Baden-Wurttemberg, Germany, 69120
    Status
    Not applicable
    Location
    Universitaetsklinik Heidelberg /ID# 50858
    Heidelberg, Baden-Wurttemberg, Germany, 69120
    Status
    Not applicable
    Location
    Universitatsklinikum Mannheim /ID# 166130
    Mannheim, Baden-Wurttemberg, Germany, 68167
    Status
    Not applicable
    Location
    Universitaetsklinikum Erlangen /ID# 34816
    Erlangen, Bavaria, Germany, 91054
    Status
    Not applicable
    Location
    Universitätsklinikum Frankfurt /ID# 53725
    Frankfurt am Main, Hesse, Germany, 60590
    Status
    Not applicable
    Location
    Universitatsklinikum Munster /ID# 205840
    Munster, Lower Saxony, Germany, 48149
    Status
    Not applicable
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