RT Journal Article
T1 How Can a Good Idea Fail? Basal Insulin Peglispro [LY2605541] for the Treatment of Type 2 Diabetes.
A1 Muñoz-Garach, Araceli
A1 Molina-Vega, María
A1 Tinahones, Francisco J
K1 Basal insulin peglispro
K1 Efficacy
K1 Hypoglycemia
K1 Pharmacodynamics
K1 Pharmacokinetics
K1 Type 2 diabetes
AB Lack of control in diabetic patients has stimulated the development of new insulin analogues. One of these was basal insulin peglispro (BIL) or LY2605541; it had a large hydrodynamic size, flat pharmacokinetic profile, half life of 2-3 days and acted preferably in the liver. We reviewed the recent literature examining the pharmacokinetics, pharmacodynamics, efficacy and safety of BIL treatment in type 2 diabetes patients. The pharmacodynamic and pharmacokinetic outline of BIL seemed to have an advantage over neutral protamine Hagedorn and glargine insulins. Recently, phase 3 studies suggested BIL was superior to glargine in reducing glucose levels in type 1 and type 2 diabetes patients in addition to causing less weight gain. It showed a different hypoglycaemia rate profile depending on the study population, with less nocturnal hypoglycaemia compared to glargine. Unfortunately, it caused higher transaminase and triglyceride levels, which led the company to discontinue development. The decision came after it had been analysed by the regulatory authorities and other external experts concerning the worse liver profile data from the IMAGINE trials. BIL was an adequate basal insulin analogue with interesting specific properties. Unfortunately the disadvantages as shown in the lipid values and liver function tests led to its failure.
SN 1869-6953
YR 2016
FD 2016-11-28
LK http://hdl.handle.net/10668/10647
UL http://hdl.handle.net/10668/10647
LA en
DS RISalud
RD Apr 6, 2025