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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01212653
Other study ID # AS_2010
Secondary ID
Status Completed
Phase Phase 4
First received September 30, 2010
Last updated September 10, 2014
Start date October 2010
Est. completion date May 2013

Study information

Verified date September 2014
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority Hong Kong: Joint CUHK-NTEC Clinical Research Ethics Committee
Study type Interventional

Clinical Trial Summary

1. To determine the effect of Golimumab treatment on the number and function of Endothelial Progenitor Cells (EPCs) in Ankylosing Spondylitis(AS) patients as a possible mechanism for the effect of this treatment on endothelial function.

2. To ascertain the effect of Golimumab treatment on , carotid intima-media thickness, vascular stiffness in Ankylosing Spondylitis(AS) patients as measured by pulse wave velocity (PWV) and Augmentation index (AIx).

3. To assess the clinical efficacy of Golimumab in Chinese Ankylosing Spondylitis(AS) patients according to ASAS response criteria at month 3, 6 and 12.

4. To perform cost-effectiveness and cost-utility analyses of the Golimumab in Ankylosing Spondylitis(AS) patients, using clinic-base data.


Description:

This study will provide important data on the pathogenesis of vascular damage and possible mechanism by which potent anti-inflammatory treatment may reduce cardiovascular risk in Ankylosing Spondylitis(AS) patients.

Fifty patients with Ankylosing Spondylitis(AS) will be randomized to receive either Golimumab or Placebo for 12 months. Patients randomized to Placebo with worsening disease activity (failure to achieve Assessment of SpondyloArthritis international Society (ASAS20)) at week 24 will be permitted to escape to open-label Golimumab. Clinical assessment, intima-media thickness, vascular stiffness and endothelial progenitor cells will be performed at baseline, 6 and 12 months.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Men or women, 18 years of age or older

- Fulfilled the modified New York diagnostic criteria for Ankylosing spondylitis (AS)for more than 3 months

- Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) = 4 (0-10 point scale), Pain visual analog scale(VAS) = 4 (0-10cm scale)

- Inadequate response to at least two Nonsteroidal Antiinflammatory Drugs (NASID) on highest recommended doses for 3 months or unable to receive full 3-month course because of intolerance,toxicity or contraindications

- Normal Chest X-ray within 3 months before baseline

- Purified Protein Derivative(PPD) negative, or Latent Tuberculosis (TB) patients were required therapy for Tuberculosis (TB) before or simultaneously with first dose of study agent

Exclusion Criteria:

- Complete ankylosis of the spine

- Concurrent with other inflammatory rheumatic disease

- Serious infection (treatment with IV-infective) within 2 months before randomization

- Active Tuberculosis (TB) or recent contact with a person with active Tuberculosis (TB)

- An opportunistic infection within 6 months of screening

- Known history of Hepatitis, Human Immunodeficiency Virus (HIV), Malignancy, a transplanted organ, multiple sclerosis, congestive heart failure

- Currently on systemic immunosuppressives, DMARDS (other than Methotrexate, Sulfasalazine , or Hydroxychloroquine), or Leflunomide within 4 week before first study agent

- Any previous use of Alefacept, Efalizumab, Rituximab, Golimumab or Natalizumab

- Use of cytotoxic drugs, received intra-articular, intramuscular, or intravenous corticosteroids in the past 4 weeks before screening

- Clinically significant renal disease (serum creatinine level = 270µmol/L), alanine aminotransferase (ALT) = 2 x upper limit of normal (ULN)

- Hemoglobin level < 8.5gm/dl, a white blood cell count < 3.5x 109/liter, a platelet count < 100x 109/liter

- Female of childbearing potential, unwilling to use adequate contraception during the study

- Pregnant or breastfeeding women

Study Design

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


Intervention

Drug:
Simponi
Golimumab 50mg monthly
Other:
0.9ml sodium chloride
0.9ml sodium chloride

Locations

Country Name City State
China Prince of Wales Hospital Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect of Golimumab treatment on the progression of subclinical atherosclerosis Effect of Golimumab treatment on the progression of subclinical atherosclerosis at 12 months compared with baseline as evaluated by Intima-Media Thickness (IMT). Month 12 Yes
Secondary Effect of Golimumab treatment on the changes in arterial stiffness Effect of Golimumab on changes in arterial stiffness at 12 months compared with baseline as evaluated by Pulse Wave Velocity and Augmentation Index. Month 12 Yes
Secondary Changes on the number and function of Endothelial Progenitor Cells in Ankylosing Spondylitis before and after 1 year of Golimumab compared with baseline. The number and function of EPCs before and after golimumab will be assessed using Wilcoxin-sign rank test Month 12 Yes
Secondary To correlate the changes in Intima-Media Thickening, Pulse Wave Velocity, Augmentation Index and Endothelial Progenitor Cells with the changes in markers of disease activity. Correlation between the change in disease activity markers (BASDAI, ESR, CRP, and MRI global activity score) and the change in IMT, PWV and AIx and EPC number will be assessed using Spearman's test Month 12 Yes
Secondary Incremental cost-utility ratio of the treatment of Golimumab. Utility will be assessed using the EuroQol 5D (EQ5D) and the Short-Form 36 (SF-36), at baseline and every visit.Utility is used to calculate quality-adjusted life years (QALYs). The incremental cost-utility ratio expressed as "(annual costs of golimumab treatment - annual costs of placebo treatment) / additional QALY gain by golimumab treatment" is calculated. Month 12 Yes