Blinatumomab
Monoclonal antibody | |
---|---|
Type | Bi-specific T-cell engager |
Source | Template:Infobox drug/mab source |
Target | CD19, CD3 |
Identifiers | |
CAS Number | 853426-35-4 |
ATC code | none |
Chemical data | |
Formula | C2367H3577N649O772S19 |
Molar mass | 54.1 kDa[[Script error: No such module "String".]] |
Blinatumomab (MT103) is a drug that has anti-cancer properties. It belongs to a new class of constructed monoclonal antibodies, bi-specific T-cell engagers (BiTEs), that exert action selectively and direct the human immune system to act against tumor cells. Blinatumomab specifically targets the CD19 antigen present on B cells.[1]
The drug was developed by a German-American company Micromet, Inc. in cooperation with MedImmune.
Structure and mechanism of action
Blinatumomab enables a patient's T cells to recognize malign B cells. A molecule of blinatumomab combines two binding sites: a CD3 site for T cells and a CD19 site for the target B cells. The drug works by linking these two cell types and activating the T cell to exert cytotoxic activity on the target cell.[2]
Therapeutic use
In a phase 1 clinical study with blinatumomab, patients with non-Hodgkin's lymphoma showed tumor regression, and in some cases complete remission.[3] There are ongoing phase 1 and phase 2 clinical trials of blinatumomab in patients with acute lymphoblastic leukemia (ALL)[4], lung or gastrointestinal cancers.[citation needed]
References
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- ↑ Statement on a Nonproprietary Name adopted by the USAN Council: Blinatumomab
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
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- ↑ ClinicalTrials.gov NCT00560794 Phase II Study of the BiTE Blinatumomab (MT103) in Patients With Minimal Residual Disease of B-precursor Acute ALL
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