Golimumab Plus UVB-311nm in Psoriasis
Primary Purpose
Psoriasis
Status
Terminated
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
UVB-311nm radiation
Sponsored by
About this trial
This is an interventional treatment trial for Psoriasis focused on measuring psoriasis, golimumab, TNF-alpha inhibition, phototherapy, 311-nm
Eligibility Criteria
Inclusion Criteria:
- Age > 18 years
- Patients with psoriatic arthritis who receive treatment with golimumab
- Patient wish for treatment of psoriatic skin lesions
Exclusion Criteria:
- Pregnancy or lactation
- Presence and/or history of malignant melanoma
- Presence and/or history of invasive squamous cell carcinoma of the skin
- Presence and/or history of more than 3 basal cell carcinomas
- Dysplastic nevus syndrome
- Antinuclear antibodies (ds-DNA, Ro/SSA, La/SSB)
- Autoimmune disorders such as lupus erythematosus or dermatomyositis
- Abnormal photosensitivity and photosensitive diseases such as porphyria, chronic actinic dermatitis, Xeroderma pigmentosum, basal cell nevus syndrome, and others
- General poor health status
Sites / Locations
- Medical University of Graz
Outcomes
Primary Outcome Measures
Psoriasis area and severity index (PASI) reduction from baseline comparing the UV-irradiated vs. the non-irradiated body site
The effect of treatment on PASI will be determined. The primary hypothesis is that UVB-311nm treatment leads to a difference in the reduction of PASI from baseline by > 20% comparing the UV-irradiated vs. the non-irradiated body site at week 6 of treatment.
Secondary Outcome Measures
Patient visual analogue (VAS) score for the therapeutic effect and severity of skin lesions
Full Information
NCT ID
NCT01088698
First Posted
March 15, 2010
Last Updated
June 23, 2014
Sponsor
Medical University of Graz
1. Study Identification
Unique Protocol Identification Number
NCT01088698
Brief Title
Golimumab Plus UVB-311nm in Psoriasis
Official Title
Prospective Study of the Combination of Golimumab and UVB-311nm Phototherapy in Patients With Psoriatic Arthritis and Psoriatic Skin Lesions
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Terminated
Why Stopped
Difficulties in recruiting patients;
Study Start Date
March 2010 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Graz
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Golimumab, a TNF-alpha antibody, has been approved in the EC and USA for the treatment of psoriatic arthritis. The aim of this study is to determine in a randomized half-side comparison whether additional narrowband UVB-311nm phototherapy accelerates and improves the clearance of psoriatic skin lesions in golimumab-treated patients.
Detailed Description
Psoriatic skin lesions of patients with psoriatic arthritis who receive standard treatment with golimumab (50 mg or 100 mg s.c. once a month depending on total body weight whether below or above 100 kg, respectively) are exposed to UVB-311nm phototherapy on a randomized body half (left or right; head exempt) 3 x per week for six weeks and/or until complete response (defined as reduction in PASI to < 3). A patient qualifies if A) golimumab was started within a week or B) after 3 months of golimumab treatment the PASI reduction is smaller than 90%. PASI score, patient visual analogue score (VAS) for therapeutic response, and patient VAS for severity of skin lesions is assessed weekly; and at follow-up visits at month 3, 6, and 12. The primary hypothesis is that phototherapy increases the PASI reduction on the exposed body site by more than 20%. Paired Wilcoxon testing for differences in PASI and patient VAS scores is done; Fisher exact test is applied to determine differences in complete remission, PASI reduction > 90%, > 75% and/or 50% between body sites.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriasis
Keywords
psoriasis, golimumab, TNF-alpha inhibition, phototherapy, 311-nm
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Radiation
Intervention Name(s)
UVB-311nm radiation
Other Intervention Name(s)
narrow-band UVB radiation
Intervention Description
UVB-311nm radiation given 3 times a week to one randomized body-half
Primary Outcome Measure Information:
Title
Psoriasis area and severity index (PASI) reduction from baseline comparing the UV-irradiated vs. the non-irradiated body site
Description
The effect of treatment on PASI will be determined. The primary hypothesis is that UVB-311nm treatment leads to a difference in the reduction of PASI from baseline by > 20% comparing the UV-irradiated vs. the non-irradiated body site at week 6 of treatment.
Time Frame
week 6
Secondary Outcome Measure Information:
Title
Patient visual analogue (VAS) score for the therapeutic effect and severity of skin lesions
Time Frame
week 6
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 18 years
Patients with psoriatic arthritis who receive treatment with golimumab
Patient wish for treatment of psoriatic skin lesions
Exclusion Criteria:
Pregnancy or lactation
Presence and/or history of malignant melanoma
Presence and/or history of invasive squamous cell carcinoma of the skin
Presence and/or history of more than 3 basal cell carcinomas
Dysplastic nevus syndrome
Antinuclear antibodies (ds-DNA, Ro/SSA, La/SSB)
Autoimmune disorders such as lupus erythematosus or dermatomyositis
Abnormal photosensitivity and photosensitive diseases such as porphyria, chronic actinic dermatitis, Xeroderma pigmentosum, basal cell nevus syndrome, and others
General poor health status
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
Organizational Affiliation
Medical University of Graz, Austria
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Graz
City
Graz
ZIP/Postal Code
8036
Country
Austria
12. IPD Sharing Statement
Learn more about this trial
Golimumab Plus UVB-311nm in Psoriasis
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