Trial Search Results
Imatinib in Systemic Sclerosis
Systemic sclerosis (SSc) is an autoimmune disease characterized by fibrosis of the skin and internal organs and widespread vasculopathy. Patients with SSc are classified according to the extent of cutaneous sclerosis: patients with limited SSc have skin thickening of the face, neck, and distal extremities, while those with diffuse SSc have involvement of the trunk, abdomen, and proximal extremities as well. The disease course varies depending on the subtype of SSc. However, common features that result in significant morbidity and mortality, in addition to cutaneous fibrosis, include Raynaud's phenomenon and digital ulcerations, interstitial lung disease (ILD), and pulmonary arterial hypertension (PAH). Current therapeutic options for patients with SSc and these clinical manifestations have shown limited efficacy.
Imatinib antagonizes specific tyrosine kinases that mediate fibrotic pathways involved in the pathogenesis of SSc, including c-Abl, a downstream mediator of transforming growth factor (TGF)-beta, and platelet derived growth factor (PDGF) receptors. The efficacy of imatinib has also been reported in the treatment of patients with refractory idiopathic PAH through its effects on vascular remodeling. Based on the mechanism of action and preliminary patient data, we hypothesize that imatinib may be effective in the treatment of the fibrotic and vasculopathic features of patients with SSc. This is an open label pilot study to evaluate the safety and efficacy of imatinib in patients with progressive SSc refractory to other treatment(s). Validated measures of skin thickness and disease activity will be determined over 6-months of therapy and compared with baseline measures.
Stanford is currently not accepting patients for this trial.
- Drug: Imatinib mesylate
Phase 1/Phase 2
Adults with refractory diffuse or limited SSc and any or all of the following: Progressive
cutaneous fibrosis, Interstitial lung disease, Pulmonary arterial hypertension, Digital
Uncontrolled congestive heart failure, hypertension, or coronary artery disease.
HIV, hepatitis B, and/or hepatitis C infection. Serious infection within the past month.
Significant hematologic, renal, or hepatic abnormalities. Concurrent use of intravenous
immunoglobulin or cyclophosphamide within 4 weeks of the first treatment dose.
Concurrent use of a biologic agent (ie. etanercept, infliximab, adalimumab, abatacept)
within 8 weeks of the first treatment dose (6 months for rituximab).
Women who are pregnant or breastfeeding.
Ages Eligible for Study
18 Years - 80 Years
Genders Eligible for Study