What we found on the web about Eculizumab
A new monoclonal antibody, eculizumab, protects blood cells against immune destruction by inhibiting the complement system. It has been shown to reduce the need for blood ...
Efalizumab (trade name Raptiva, Genentech, Merck Serono) is a medication designed to ... Certolizumab pegol, Daclizumab, Eculizumab, Efalizumab, Epratuzumab, Erlizumab, Fontolizumab, ...
This study will evaluate the safety and effectiveness of the experimental drug eculizumab for treating paroxysmal nocturnal hemoglobinuria (PNH), a disorder that can cause ...
The purpose of this study is to determine whether eculizumab is safe and effective in the treatment of patients with generalized myasthenia gravis despite treatment with various ...
1: N Engl J Med. 2006 Sep 21;355(12):1233-43. Comment in: N Engl J Med. 2006 Dec 28;355(26):2786; author reply 2787-8. N Engl J Med. 2006 Dec 28;355(26):2786; author reply 2787-8.
Eculizumab affects your immune system, and using this medication may increase your risk of serious infection such as meningitis. Get emergency medical help if you have any signs of ...
B lueCross BlueShield of Tennessee Medical Policy Manual. Eculizumab. DESCRIPTION. Eculizumab, a recombinant monoclonal antibody, binds to the complement protein C5 and inhibits ...
FDA approves Soliris for the treatment of paroxysmal nocturnal hemoglobinuria. On March 16, 2007 the U.S. Food and Drug Administration granted approval to eculizumab injection ...
Here is what users have to say about Eculizumab

Eculizumab (INN and USAN, trade name Soliris) is a monoclonal antibody directed against the complement protein C5. This antibody blocks the cleavage of C5 and halts the process of complement-mediated cell destruction. Eculizumab is a product of Alexion Pharmaceuticals and has been shown to be effective in treating paroxysmal nocturnal hemoglobinuria. Eculizumab was approved by the United States Food and Drug Administration (FDA) on March 16, 2007 and was later approved by the European Medicines Agency on June 20, 2007.

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