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Drug Metabolism and Disposition Fast Forward
First published on May 17, 2007; DOI: 10.1124/dmd.106.013797


0090-9556/07/3508-1418-1428$20.00
DMD 35:1418-1428, 2007

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Absorption, Distribution, Metabolism, and Elimination of the Direct Renin Inhibitor Aliskiren in Healthy Volunteers

Felix Waldmeier, Ulrike Glaenzel, Bernard Wirz, Lukas Oberer, Dietmar Schmid, Michael Seiberling, Jessica Valencia, Gilles-Jacques Riviere, Peter End, and Sujata Vaidyanathan

Novartis Pharma AG, Basel, Switzerland (F.W., U.G., B.W., L.O., D.S., P.E.); Swiss Pharma Contract Ltd., Allschwil, Switzerland (M.S.); Novartis Pharmaceuticals Corporation, East Hanover, New Jersey (J.V., S.V.); and Novartis Pharma SAS, Rueil-Malmaison, France (G.-J.R.)

Aliskiren (2(S),4(S),5(S),7(S)-N-(2-carbamoyl-2-methylpropyl)-5-amino-4-hydroxy-2,7-diisopropyl-8-[4-methoxy-3-(3-methoxypropoxy)phenyl]-octanamid hemifumarate) is the first in a new class of orally active, nonpeptide direct renin inhibitors developed for the treatment of hypertension. The absorption, distribution, metabolism, and excretion of [14C]aliskiren were investigated in four healthy male subjects after administration of a single 300-mg oral dose in an aqueous solution. Plasma radioactivity and aliskiren concentration measurements and complete urine and feces collections were made for 168 h postdose. Peak plasma levels of aliskiren (Cmax) were achieved between 2 and 5 h postdose. Unchanged aliskiren represented the principal circulating species in plasma, accounting for 81% of total plasma radioactivity (AUC0–{infty}), and indicating very low exposure to metabolites. Terminal half-lives for radioactivity and aliskiren in plasma were 49 h and 44 h, respectively. Dose recovery over 168 h was nearly complete (91.5% of dose); excretion occurred almost completely via the fecal route (90.9%), with only 0.6% recovered in the urine. Unabsorbed drug accounted for a large dose proportion recovered in feces in unchanged form. Based on results from this and from previous studies, the absorbed fraction of aliskiren can be estimated to approximately 5% of dose. The absorbed dose was partly eliminated unchanged via the hepatobiliary route. Oxidized metabolites in excreta accounted for at least 1.3% of the radioactive dose. The major metabolic pathways for aliskiren were O-demethylation at the phenyl-propoxy side chain or 3-methoxy-propoxy group, with further oxidation to the carboxylic acid derivative.


Address correspondence to: Dr. Felix Waldmeier, Novartis Pharma AG, WSJ-210.4.20, Novartis Campus, CH-4056 Basel, Switzerland. E-mail: felix.waldmeier{at}novartis.com




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