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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00420303
Other study ID # 0881A3-404
Secondary ID
Status Completed
Phase Phase 4
First received January 8, 2007
Last updated July 15, 2010
Start date January 2007
Est. completion date September 2008

Study information

Verified date July 2010
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)France: Institutional Ethical CommitteeGermany: Ethics CommissionGermany: Federal Institute for Drugs and Medical DevicesNetherlands: Independent Ethics CommitteeNetherlands: Medicines Evaluation Board (MEB)
Study type Interventional

Clinical Trial Summary

To assess the efficacy and safety of Etanercept in patients with spondylarthropathy and refractory heel enthesitis.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion criteria

- Spondylarthropathy

- Heel enthesitis refractory to standard treatment

- Between 18 and 70 years of age

- The patient global assessment of the disease activity (measured by a 100 mm VAS) must be >40 in the last 48 hours

Exclusion criteria

- Use of > 1 local steroid injection within 2 weeks of screening

- Prior exposure to any TNF-inhibitor, including etanercept

- Dose of NSAIDs changed within two weeks of study drug evaluation

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Etanercept
50 mg injection once weekly
Other:
Placebo
placebo

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Countries where clinical trial is conducted

France,  Germany,  Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Normalized Net Incremental Area Under the Curve (AUC) for Patient Global Assessment of Disease Activity (PGA) Between Randomization and Week 12 PGA was measured using a 100mm Visual Analog Scale (VAS) ranging from 0=very good to 100=very bad. The normalized net incremental area under the curve of the PGA is the area between the baseline and the PGA curve as a function of time (week 2, 4, 8, 12). AUC was computed using the linear trapezoidal method. All the areas above the baseline and under the curve are positive and all the area below the baseline and above the curve are negative. The net incremental AUC is the sum of these areas. This result is then divided by the study duration of the patients. (negative value = improvement). 12 weeks No
Primary Change From Baseline in Patient Global Assessment of Disease Activity Score at Week 12 The patient global assessment of disease activity was measured using a 100mm Visual Analog Scale (VAS) ranging from 0=very good to 100=very bad. Change=12 week score minus baseline score. A negative score indicates an improvement in disease activity and a positive score indicates worsening. Baseline and 12 weeks No
Secondary Number of Patients Achieving a 50% Response on the Patient Global Assessment of Disease Activity A response is defined as at least a 50% improvement (decrease) from baseline in the patient global assessment of disease activity. The patient global assessment of disease activity was measured using a 100mm Visual Analog Scale (VAS) ranging from 0=very good to 100=very bad. 12 weeks No