Skip to content

Safety and Effectiveness and Effect on Quality of Life and Work Productivity of Humira in Patients With Psoriatic Arthritis in Clinical Routine

Long Term Documentation of the Safety and Efficacy as Well as the Effects on Quality of Life and Work Productivity in Patients With Psoriatic Arthritis Under HUMIRA® (Adalimumab) in Routine Clinical Practice

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01078610
Acronym
ELAN
Enrollment
0
Registered
2010-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2012-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriatic Arthritis

Keywords

Psoriatic Arthritis, Long-term Observation, Humira, Safety, Effectiveness, Quality of Life, Work Productivity

Brief summary

Safety and effectiveness, quality of life and work productivity of Humira in patients with psoriatic arthritis in clinical routine.

Detailed description

The primary objective of the Non-Interventional Study is to explore the therapeutic success, measured by improvements in the following target variables (with regard to the respective baseline value): * The number of missed working days * The self-assessed workability * The severity of clinical symptoms (number of tender and swollen joints, C-reactive Protein and erythrocyte sedimentation rate respectively; total score Disease Activity Score 28, Psoriasis Area and Severity Index) * The severity of functional impairment (Health Assessment Questionnaire) * The health-related quality of life . All of the patient and disease characteristics which are documented at baseline will be evaluated for their additional impact on the target variables (therapeutic success). Particularly the impact of previous biologic therapies on clinical target variables will be evaluated. The secondary objective is to document the therapeutic success by the following variables: * The number of physician visit * The number and duration of hospitalization * The number of days of impairment in non-occupational activities * Pain, exhaustion/fatigue * The reduction of number and dose of concomitant medication * Patient's assessment of adalimumab therapy compared to previous therapies. Target parameters for safety evaluation of adalimumab are: * The evaluation of safety and tolerability by the documentation and analysis of serious adverse events (SAEs) and adverse events (AEs) * Evaluation of safety and tolerability for subgroups of patients with common frequent concomitant diseases, especially diabetes type II, cardiovascular, liver, and renal insufficiencies, and related concomitant medications.

Interventions

40 mg adalimumab (Humira) every other week.

Sponsors

Abbott
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Active and progressive psoriatic arthritis in adults with insufficient response to prior basic 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.

Design outcomes

Primary

MeasureTime frame
Improvement in: number of missed working days, self-assessed workability, severity of clinical symptoms and functional impairment, health-related quality of life; safety an tolerability: documentation of adverse events and serious adverse eventsMonths 0, 3, 6, 12, 24, 36, 48, 60

Secondary

MeasureTime frame
Number and duration of hospitalization; reduction of number and dose of concomitant medication: patient's assessment of adalimumab therapy compared to previous therapies.Months 0, 3, 6, 12, 24, 36, 48, 60

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026