Journal
GROWTH HORMONE & IGF RESEARCH
Volume 33, Issue -, Pages 9-16Publisher
CHURCHILL LIVINGSTONE
DOI: 10.1016/j.ghir.2017.01.001
Keywords
IGF-1; PEG-IGF-1; GH feedback loop; Hypoglycemia; Elongated half life
Categories
Funding
- F. Hoffmann-La Roche Ltd.
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Objective: This study is a first time assessment of safety and tolerability, pharmacokinetics, and pharmacodynamics of R05046013 in human, in comparison with unmodified rhIGF-L Design: The study was conducted as a single-center, randomized, double-blinded, placebo-controlled, single ascending dose, parallel group study in a clinical research unit in France. A total of 62 healthy volunteers participated in this clinical trial. R05046013 was given as single subcutaneous injection, or as intravenous infusion over 48 h, at ascending dose levels. The active comparator rhIGF-I was administered at 50 mu g/kg subcutaneously twice daily for 4 days. Safety and tolerability, pharmacokinetics, and pharmacodynamics of R05046013 were evaluated. Results: PEGylation resulted in long exposure to R05046013 with a half-life of 140-200 h. Exposure to R05046013 increased approximately dose proportionally. R05046013 was safe and well tolerated at all doses, injection site erythema after SC administration was the most frequent observed AE. No hypoglycemia occurred. Growth hormone (GH) secretion was almost completely suppressed with rhIGF-I administration, whereas R05046013 caused only a modest decrease in GH at the highest dose given IV. Conclusions: PEGylation of IGF-I strongly enhances half-life, reduces the negative GH feedback and hypoglycemia potential, and therefore offers a valuable alternative to rhIGF-I in treatment of relevant diseases. (C) 2017 Elsevier Ltd. All rights reserved.
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