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Engineering of a GLP-1 analogue peptide/anti-PCSK9 antibody fusion for type 2 diabetes treatment.
- Source :
-
Scientific reports [Sci Rep] 2018 Dec 03; Vol. 8 (1), pp. 17545. Date of Electronic Publication: 2018 Dec 03. - Publication Year :
- 2018
-
Abstract
- Type 2 diabetes (T2D) is a complex and progressive disease requiring polypharmacy to manage hyperglycaemia and cardiovascular risk factors. However, most patients do not achieve combined treatment goals. To address this therapeutic gap, we have developed MEDI4166, a novel glucagon-like peptide-1 (GLP-1) receptor agonist peptide fused to a proprotein convertase subtilisin/kexin type 9 (PCSK9) neutralising antibody that allows for glycaemic control and low-density lipoprotein cholesterol (LDL-C) lowering in a single molecule. The fusion has been engineered to deliver sustained peptide activity in vivo in combination with reduced potency, to manage GLP-1 driven adverse effects at high dose, and a favourable manufacturability profile. MEDI4166 showed robust and sustained LDL-C lowering in cynomolgus monkeys and exhibited the anticipated GLP-1 effects in T2D mouse models. We believe MEDI4166 is a novel molecule combining long acting agonist peptide and neutralising antibody activities to deliver a unique pharmacology profile for the management of T2D.
- Subjects :
- Animals
CHO Cells
Cricetulus
Hep G2 Cells
Humans
Macaca fascicularis
Male
Mice
Antibodies, Monoclonal pharmacokinetics
Antibodies, Monoclonal pharmacology
Diabetes Mellitus, Experimental blood
Diabetes Mellitus, Experimental drug therapy
Diabetes Mellitus, Type 2 blood
Diabetes Mellitus, Type 2 drug therapy
Glucagon-Like Peptide 1
Hypoglycemic Agents pharmacokinetics
Hypoglycemic Agents pharmacology
PCSK9 Inhibitors
Recombinant Fusion Proteins pharmacokinetics
Recombinant Fusion Proteins pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 30510163
- Full Text :
- https://doi.org/10.1038/s41598-018-35869-4