Blisibimod

Blisibimod

Blisibimod

Clinical data
Pregnancy cat.	-
Legal status	Investigational
Identifiers
CAS number	1236126-45-6
ATC code	None
Synonyms	A-623
Chemical data
Formula	?
Mol. mass	63.6 kDa
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Blisibimod (also known as A-623, formerly AMG 623) is a selective peptibody antagonist of B-cell activating factor (BAFF, also known as B-Lymphocyte Stimulator or BLyS), being developed by Anthera Pharmaceuticals as a treatment for systemic lupus erythematosus. It is currently under active investigation in clinical trials.

Mechanism

Blisibimod is a peptibody consisting of four novel BAFF binding domains fused to the N-terminus of the fragment crystallizable region (Fc) of a human antibody.

BAFF is involved in B-cell survival, activation, and differentiation. Elevated levels of BAFF have been associated with several B-cell mediated autoimmune diseases, including systemic lupus erythematosus, lupus nephritis, rheumatoid arthritis, multiple sclerosis, Sjögren’s syndrome, Graves’ disease, and Hashimoto's thyroiditis. Blisibimod binds to BAFF and inhibits interaction with BAFF receptors, thus decreasing B-cell survival and proliferation throughout the body. Improvements in disease activity have been observed in patients with systemic lupus erythematosus and rheumatoid arthritis following treatment with BAFF inhibitors in clinical trials.

Development

Blisibimod was initially developed by Amgen, with Phase I trials demonstrating comparable safety between the blisibimod and placebo treatments. Blisibimod was acquired by Anthera Pharmaceuticals, who in 2010 initiated a global Phase II study entitled PEARL-SC to investigate the efficacy, safety, and tolerability of blisibimod in subjects with systemic lupus erythematosus. As of 2011, this study is ongoing.

References

Retrieved from : http://en.wikipedia.org/wiki/Blisibimod