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Bone and Cancer

Clinical Trials

Sylvant (siltuximab)

The following drug information is obtained from various newswires, published medical journal articles, and medical conference presentations.

Company:

Approval Status:

Approved April 2014

Specific Treatments:

multicentric Castleman’s disease

Therapeutic Areas

General Information

Sylvant (siltuximab) is an anti-interleukin-6 (IL-6) chimeric monoclonal antibody that binds to human IL-6.1 IL-6 is a multifunctional cytokine produced by various cells such as T cells, B cells, monocytes, fibroblasts and endothelial cells. Dysregulated overproduction of IL-6 from activated B cells in affected lymph nodes has been implicated in the pathogenesis of, or mechanism causing, multicentric Castleman's disease.

Sylvant is specifically indicated for the treatment of patients with multicentric Castleman’s disease who are human immunodeficiency virus (HIV) negative and human herpesvirus-8 (HHV-8) negative.

Sylvant is supplied as a solution for intravenous infusion. The recommended dose is 11 mg/kg is given over 1 hour as an intravenous infusion administered every three weeks until treatment failure.

Clinical Results

FDA Approval
The FDA approval of Sylvant was based on a phase II, multinational, randomized, double blind, placebo controlled study. In this study 53 subjectswere randomized to Best Supportive Care (BSC) and Sylvant at a dose of 11 mg/kg every 3 weeks and 26 subjects were randomized to BSC and placebo. Treatment was continued until treatment failure (defined as disease progression based on increase in symptoms, radiologic progression or deterioration in performance status) or unacceptable toxicity. The major efficacy outcome of the study was durable tumor and symptomatic response, defined as tumor response assessed by independent review and complete resolution or stabilization of MCD symptoms. A durable response was defined as tumor and symptomatic response that persisted for a minimum of 18 weeks without treatment failure. The durable tumor and symptomatic response in the Sylvant arm was 34% compared to 0% in the placebo arm (p=0.0012).

Side Effects

Adverse effects associated with the use of Sylvant may include, but are not limited to, the following:

  • pruritus
  • increased weight
  • rash
  • hyperuricemia
  • upper respiratory tract infection

Mechanism of Action

Sylvant (siltuximab) binds human IL-6 and prevents the binding of IL-6 to both soluble and membrane-bound IL-6 receptors IL-6 has been shown to be involved in diverse normal physiologic processes such as induction of immunoglobulin secretion. Overproduction of IL-6 has been linked to systemic manifestations in patients with MCD.

Additional Information

For additional information regarding Sylvant or multicentric Castleman's disease, please visit the Sylvant web page.

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