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Treatment of Patients With Nephrogenic Systemic Fibrosis With Glivec

An Open Label Clinical Trial of Imatinib Mesylate(Glivec)in Patients With Moderate to Severe Nephrogenic Systemic Fibrosis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00981942
Acronym
NSF
Enrollment
10
Registered
2009-09-22
Start date
2009-09-30
Completion date
2010-12-31
Last updated
2012-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nephrogenic Systemic Fibrosis

Keywords

Nephrogenic systemic fibrosis, Imatinib mesylate, Glivec, Gleevec

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.

Interventions

400 mg, one tablet daily for 12 or 24 weeks

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age \> 18 years 2. Diagnosed with NSF 3. mRodnan skin score =\> 20 or 4. Rapid progression of the disease defined as a 50% increase in mRodnan skin score in less than 7 weeks or 5. Progression of the fibrosis in the inner organs ex. the heart or the lungs, AND 6. No absolute contraindications to the treatment

Exclusion criteria

1. Known sensitivity to Imatinib mesylate or to any of its components 2. Pregnant or lactating woman 3. ALAT \> 3 x upper limit of normal 4. Severe congestive heart failure (NYHA Class III or IV)

Design outcomes

Primary

MeasureTime frame
The primary endpoints are skin fibrosis and joint mobility.16 weeks or 28 weeks

Secondary

MeasureTime frame
The secondary endpoint is and joint mobility.16 weeks or 28 weeks

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026