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The Influence of Adalimumab on Cardiovascular and Metabolic Risk in Psoriasis (CASTIP)

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Medical University of Vienna

Status and phase

Unknown
Phase 4

Conditions

Psoriasis
Cardiovascular Diseases
Diabetes Mellitus, Type 2

Treatments

Other: Narrow band UVB radiation
Drug: Adalimumab treatment arm
Drug: Fumaric acid esters treatment group

Study type

Interventional

Funder types

Other

Identifiers

NCT01088165
CASTIP1

Details and patient eligibility

About

Psoriasis vulgaris is no longer considered as a chronic inflammatory disease restricted to the skin. Evidence has accumulated in the past that psoriasis is a chronic inflammatory systemic disease. As in rheumatoid arthritis, the chronic inflammatory process plays a central role in the pathogenesis of associated comorbidities such as diabetes and cardiovascular disease. Since several years the armamentarium of psoriasis treatment has been broadened by the availability of TNF alpha blockers. These neutralize systemic TNF alpha which not only plays a central role in the pathogenesis of psoriasis but has also been linked to inflammatory pathways in diabetes and cardiovascular disease. While a few studies have investigated the positive effects of TNF alpha blockers on associated cardiovascular disease in rheumatoid arthritis patients, no research data exist on the effects of these therapeutic agents in patients with moderate to severe chronic plaque psoriasis.

The present study aims at determining the effects of adalimumab, a potent and frequently prescribed TNF alpha blocker for the treatment of psoriasis, on different diabetic and cardiovascular risk factors in patients receiving this treatment as a remedy for moderate to severe plaque type psoriasis. The study is designed to explore whether adalimumab is capable to prevent or modulate psoriasis-associated comorbidities by blocking systemic inflammation. The effects of adalimumab will be compared with those of fumaric acids, which represent an established traditional systemic treatment option for moderate to severe psoriasis.

Study hypothesis:

Therapy with adalimumab will lead to an improvement of several parameters that reflect the risk for diabetes and cardiovascular disease in patients with chronic plaque psoriasis due to chronic inflammation. Endothelial dysfunction, as assessed by ultrasound flow mediated dilatation, will serve as primary outcome measure. Other risk factors such as blood lipids, hsCRP, IL-6, endothelial adhesion molecules, parameters of glucose metabolism and carotid intima-media thickness will be secondary outcomes.

Aim:

If adalimumab and/or fumaric acids will show a significant impact on the above mentioned parameters, these findings would offer a new perspective for the long term management of psoriatic patients and their comorbidities.

Study design: Randomized, prospective, controlled, parallel group study

Study population: 66 patients

Enrollment

66 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic severe plaque type psoriasis (PASI <10) requiring systemic treatment. Non-response or contraindication to previous systemic and/or light treatment
  • PASI ≥ 10, BSA ≥ 10
  • Age 18 - 80 years

Exclusion criteria

  • Women of childbearing potential not taking contraceptive measures
  • Pregnant or breastfeeding women
  • Patients with a history or ongoing malignancy, chronic infections or autoimmune disease
  • Patients with severe impairment of their general health
  • Patients who are unable to understand or comply with the study protocol

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

66 participants in 2 patient groups

Adalimumab treatment group
Experimental group
Treatment:
Drug: Adalimumab treatment arm
Other: Narrow band UVB radiation
Fumaric acid esters treatment group
Active Comparator group
Treatment:
Drug: Fumaric acid esters treatment group
Other: Narrow band UVB radiation

Trial contacts and locations

1

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Central trial contact

Adrian Tanew, MD; Gregor Holzer, MD

Data sourced from clinicaltrials.gov

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