Planta Med 2005; 71(10): 891-896
DOI: 10.1055/s-2005-864186
Original Paper
Clinical Study
© Georg Thieme Verlag KG Stuttgart · New York

Repeated Oral Once Daily Intake of Increasing Doses of the Novel Synthetic Genistein Product Bonistein™ in Healthy Volunteers

U. Ullmann1 , H. Oberwittle2 , M. Grossmann2 , C. Riegger1
  • 1DSM Nutritional Products Ltd, R&D Human Nutrition & Health, Kaiseraugst, Switzerland
  • 2Institute for Clinical Pharmacology Bobenheim Prof. Dr. Luecker GmbH, Grünstadt, Germany
Further Information

Publication History

Received: January 18, 2005

Accepted: February 2, 2005

Publication Date:
29 July 2005 (online)

Abstract

Bonistein™ is a new product consisting of > 99.5 % synthetic genistein, an isoflavone with phyto-oestrogenic properties, which might be a safe and efficacious alternative for the prevention of post-menopausal bone loss to the traditional hormone replacement therapy. A randomised, open-labelled and sequential-group phase I study was performed to assess safety, tolerability and pharmacokinetic characteristics of oral administrations of Bonistein™. Thirty healthy volunteers received in three subsequent groups 30, 60 or 120 mg once daily for 14 days. For the pharmacokinetic profiles of Bonistein™, blood samples were taken on study Days 1 (after first dose) and 14 (steady state). Repeated intake of Bonistein™ was well tolerated. A total of 33 adverse events were reported, mainly of mild intensity. No relevant changes in clinical laboratory or vital signs were observed. The pharmacokinetic characteristics of Bonistein™ revealed comparable results for extent and rate of absorption on Days 1 and 14. Both AUC and Cmax values of Bonistein™ increased in proportion with the dose.

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Uwe Ullmann, MD

DSM Nutritional Products

R&D Human Nutrition & Health

4303 Kaiseraugst

Switzerland

Phone: +41-61-68-88798

Fax: +41-61-68-89684

Email: uwe.ullmann@dsm.com

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