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Antimicrobial Agents and Chemotherapy, January 2006, p. 286-293, Vol. 50, No. 1
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.1.286-293.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Multiple-Dose Pharmacokinetics and Safety of the New Antifungal Triazole BAL4815 after Intravenous Infusion and Oral Administration of Its Prodrug, BAL8557, in Healthy Volunteers

Anne Schmitt-Hoffmann,^1* Brigitte Roos,¹ Jürgen Maares,¹ Markus Heep,¹ Jochen Spickerman,¹ Erhard Weidekamm,¹ Tom Brown,¹ and Michael Roehrle²

Basilea Pharmaceutica, Ltd., 4002 Basel, Switzerland,¹ AAI, 89231 Neu-Ulm, Germany²

Received 21 April 2005/ Returned for modification 25 May 2005/ Accepted 27 September 2005

BAL8557 is the water-soluble prodrug of BAL4815, a new broad-spectrum antifungal. Healthy male subjects were randomly assigned to four treatment cohorts to receive multiple oral doses or multiple 1-h constant-rate intravenous infusions of BAL8557. Loading doses of BAL8557 were equivalent to 100 mg (followed by once-daily maintenance doses of 50 mg) or 200 mg (followed by once-daily maintenance doses of 100 mg) of BAL4815. In each cohort, six subjects received active drug and two subjects received the placebo. Study duration was 21 days (oral) and 14 days (intravenous). All adverse events reported were mild or moderate, except one severe rhinitis event which was not related to trial medication. After both routes of administration, maximum drug concentration observed in plasma (C_max) and area under the concentration-time curve (AUC) values of BAL4815 increased proportionally to the administered dose. AUC values reflected a fourfold to fivefold accumulation of active drug in plasma during once-daily dosing, which is in line with the long elimination half-life of BAL4815 determined after the last administration (mean, 84.5 to 117 h). At steady state, the volume of distribution was large and amounted to 308 to 542 liters. Systemic clearance reached only 2.4 to 4.1 liter/h. At the levels obtained in the present study, C_max values of 2.56 and 2.55 µg/ml after oral and intravenous administrations, respectively, there was no indication of CYP3A4 induction or inhibition (as revealed by the urinary 6-ß-hydroxycortisol/cortisol test). Based on AUC values after oral and intravenous administration, an excellent oral bioavailability can be predicted for BAL4815. Once-daily oral dosing of 50- or 100-mg equivalents of BAL8557 were recently demonstrated to be efficacious in a phase 2 study conducted with patients with esophageal candidiasis. These doses (preceded by adequate loading dose[s]) will be further explored in the treatment of systemic mycoses.

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* Corresponding author. Mailing address: Basilea Pharmaceutica, Ltd., P.O. Box 3255, 4002 Basel, Switzerland. Phone: 41 61 606 1379. Fax: 41 61 606 1378. E-mail: schmita{at}basileapharma.com.

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Antimicrobial Agents and Chemotherapy, January 2006, p. 286-293, Vol. 50, No. 1
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.1.286-293.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

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