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Louis McMahon

Researcher at Novartis

Publications -  8
Citations -  1291

Louis McMahon is an academic researcher from Novartis. The author has contributed to research in topics: Everolimus & Transplantation. The author has an hindex of 7, co-authored 8 publications receiving 1262 citations.

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mTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathways

TL;DR: It is reported that mTOR inhibition induced apoptosis of epithelial cells and the complete reversal of a neoplastic phenotype in the prostate of mice expressing human AKT1 in the ventral prostate, and that clinical resistance to mTOR inhibitors may emerge through BCL2 expression and/or upregulation of HIF-1α activity.
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Population pharmacokinetics of everolimus in de novo renal transplant patients: impact of ethnicity and comedications.

TL;DR: Everolimus is a macrolide immunosuppressant intended for acute rejection prophylaxis after kidney transplantation.
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High-throughput semi-automated 96-well liquid/liquid extraction and liquid chromatography/mass spectrometric analysis of everolimus (RAD 001) and cyclosporin a (CsA) in whole blood.

TL;DR: A marked improvement in sample throughput efficiency was realized with this LLE method when compared to existing solid phase extraction (SPE) methods which deal with both RAD001 and CsA.
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Pharmacokinetics of an everolimus-cyclosporine immunosuppressive regimen over the first 6 months after kidney transplantation.

TL;DR: Everolimus exposure was relatively stable over the first 6’months post transplant, with no major departure from dose‐proportionality over the therapeutic dose range, and weight‐adjusted dosing (mg/kg) does not appear warranted.
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High‐throughput analysis of everolimus (RAD001) and cyclosporin A (CsA) in whole blood by liquid chromatography/mass spectrometry using a semi‐automated 96‐well solid‐phase extraction system

TL;DR: The sensitivity, small sample volume needed and high sample throughput of this liquid chromatography/mass spectrometry procedure make it an attractive option for pharmacokinetic studies in pediatric patients.