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Ocrelizumab

Ocrelizumab Suppliers list
Company Name: Wuhan Maixi Biotechnology Co., Ltd  Gold
Tel: 18007167883 18007167883
Email: Service@mabnus.com
Company Name: Wuhan Sunrise Technology Development Co., Ltd.  
Tel: 27-027-83314682 13554138826
Email: whsrtech@vip.163.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Dalian Meilun Biotech Co., Ltd.  
Tel: 0411-62910999 13889544652
Email: sales@meilune.com
Company Name: Nanjing Sunlida Biological Technology Co., Ltd.  
Tel: 025-57798810 18652991625
Email: sales@sunlidabio.com
Ocrelizumab Basic information
Product Name:Ocrelizumab
Synonyms:Ocrelizumab;Research Grade Ocrelizumab(DHC90702);Ocrelizumab (anti-CD20);Research Grade Ocrelizumab;PRO70769;RG1594
CAS:637334-45-3
MF:C19H16N2O5
MW:0
EINECS:
Product Categories:
Mol File:Mol File
Ocrelizumab Structure
Ocrelizumab Chemical Properties
form Liquid
color Colorless to light yellow
Safety Information
Hazardous Substances Data637334-45-3(Hazardous Substances Data)
MSDS Information
Ocrelizumab Usage And Synthesis
HistoryThe development of Ocrelizumab, sold under the brand name Ocrevus, starts with rituximab, another monoclonal antibody (MAb) that was developed for the treatment of autoimmune disorders and was approved for the treatment of CD20-positive follicular non-Hodgkin lymphoma in 1994. However, rituximab is a chimeric MAb and is immunogenic in humans, and the manufacturer decided to focus on the similar but fully humanized MAb, ocrelizumab, for multiple sclerosis instead. It was granted approval by the U.S. Food and Drug Administration (FDA) in 2017 as the first treatment indicated for both relapsing and primary progressive forms of multiple sclerosis.Ocrelizumab has also been approved by the European Medicines Agency.
UsesTreatment of rheumatoid arthritis.
in vivo

Ocrelizumab (7.5 mg/kg; once daily; 18 days; s.c. or i.v.) inhibits lesions in multiple sclerosis mice by inducing B cell exhaustion through antibody dependent cytotoxicity (ADCC)[1]. Ocrelizumab (50 μg; repeat administration on days 7, 14, and 21; i.v.) can reduce B and T cells in the blood, lymph nodes, and spleen of C57BL/6 mice[2].

Animal Model:HuCD20 mice with chronic DTH-TLS lesions[1].
Dosage:7.5 mg/kg
Administration:Subcutaneous injection (s.c.) or intravenous injection (i.v.); once daily; 18 days; initiated on Days 63, 70 and 75 post lesion induction
Result:Reduced the number of CD19+ cells and MS like lesions in the spleen and lymph nodes of mice.
Animal Model:C57BL/6 mice [2].
Dosage:50 μg
Administration:Intravenous injection (i.v.); repeat administration on days 7, 14, and 21
Result:Reduced the total CD19+ B cells and CD4, CD8 T cells in the blood, spleen, and LN.
Ocrelizumab Preparation Products And Raw materials
Tag:Ocrelizumab(637334-45-3) Related Product Information
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