Treatment of Patients With Nephrogenic Systemic Fibrosis With Glivec (NSF)
Primary Purpose
Nephrogenic Systemic Fibrosis
Status
Completed
Phase
Phase 3
Locations
Denmark
Study Type
Interventional
Intervention
Imatinib mesylate (Glivec)
Sponsored by
About this trial
This is an interventional treatment trial for Nephrogenic Systemic Fibrosis focused on measuring Nephrogenic systemic fibrosis, Imatinib mesylate, Glivec, Gleevec
Eligibility Criteria
Inclusion criteria:
- Age > 18 years
- Diagnosed with NSF
- mRodnan skin score => 20 or
- Rapid progression of the disease defined as a 50% increase in mRodnan skin score in less than 7 weeks or
- Progression of the fibrosis in the inner organs ex. the heart or the lungs, AND
- No absolute contraindications to the treatment
Exclusion Criteria:
- Known sensitivity to Imatinib mesylate or to any of its components
- Pregnant or lactating woman
- ALAT > 3 x upper limit of normal
- Severe congestive heart failure (NYHA Class III or IV)
Sites / Locations
- Department of Dermatology
Outcomes
Primary Outcome Measures
The primary endpoints are skin fibrosis and joint mobility.
Secondary Outcome Measures
The secondary endpoint is and joint mobility.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00981942
Brief Title
Treatment of Patients With Nephrogenic Systemic Fibrosis With Glivec
Acronym
NSF
Official Title
An Open Label Clinical Trial of Imatinib Mesylate(Glivec)in Patients With Moderate to Severe Nephrogenic Systemic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators will study the effect of imatinib mesylate (Glivec) in treatment of moderate to severe nephrogenic systemic fibrosis (NSF).
So far there is no evidence of adequately effective treatment options of NSF. Various treatments have been tried to stop the progressing disease. Corticosteroids, which suppress the early inflammatory stage of the disease, fail to halt disease progression.
Other immunosuppressive agents, photopheresis, and kidney transplantations are reported to be partly beneficial to the patients.
It has not been possible to confirm these findings in further studies because in photopheresis, and kidney transplantation, such effects are generally unreproducible.
Detailed Description
NSF is a relatively newly defined fibrosing disease not described before 1997 where the Gadolinium-based contrast agents (GBCAs) were introduced in patients with kidney disease. The association between NSF and GBCA has in many studies shown to be very strong. Until recently, radiologists believed that commercially available GBCAs were safe to use whether the renal function was normal or not. Since the 1980s, >200 million patients have been given these agents. Lately, the occurrence of NSF, a relatively new chronic disorder, has given serious speculations about the safety of these drugs and has questioned their future use. First identified in 1997, but not described until 2000, NSF has been reported only in patients with acute or chronic severe renal insufficiency (with a glomerular filtration rate <30 ml/min/1.73 m2).
Fibrosis in the subcutis means that the skin hardens and loses flexibility. Hard dermal plaque changes often appear on legs, arms and abdomen together with dyspigmentation. As the lesions involve the deep part of the subcutis the muscles are often affected. Involvement of the joints leads to contractures and narrowing of movement. Patients with massive affection of the joints often end up with a zimmer frame or in a wheelchair. The connecting tissue in the inner vital organs may also be affected and NSF can accelerate the death of the patient. The retained gadolinium in lesions of NSF can be found years after administration.
Interestingly, a case report suggests beneficial effects of imatinib mesylate in two patients. Two other independent case reports also show promising results.
Imatinib mesylate inhibits several tyrosine kinases involved in the fibrotic reaction, which is one of the main pathogenetic components of NSF.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephrogenic Systemic Fibrosis
Keywords
Nephrogenic systemic fibrosis, Imatinib mesylate, Glivec, Gleevec
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Imatinib mesylate (Glivec)
Other Intervention Name(s)
Glivec, Gleevec
Intervention Description
400 mg, one tablet daily for 12 or 24 weeks
Primary Outcome Measure Information:
Title
The primary endpoints are skin fibrosis and joint mobility.
Time Frame
16 weeks or 28 weeks
Secondary Outcome Measure Information:
Title
The secondary endpoint is and joint mobility.
Time Frame
16 weeks or 28 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Age > 18 years
Diagnosed with NSF
mRodnan skin score => 20 or
Rapid progression of the disease defined as a 50% increase in mRodnan skin score in less than 7 weeks or
Progression of the fibrosis in the inner organs ex. the heart or the lungs, AND
No absolute contraindications to the treatment
Exclusion Criteria:
Known sensitivity to Imatinib mesylate or to any of its components
Pregnant or lactating woman
ALAT > 3 x upper limit of normal
Severe congestive heart failure (NYHA Class III or IV)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne B Olesen, MD,PhD
Organizational Affiliation
Anne Braae Olesen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Dermatology
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
18668587
Citation
Kay J, High WA. Imatinib mesylate treatment of nephrogenic systemic fibrosis. Arthritis Rheum. 2008 Aug;58(8):2543-8. doi: 10.1002/art.23696.
Results Reference
background
Learn more about this trial
Treatment of Patients With Nephrogenic Systemic Fibrosis With Glivec
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