An official website of the United States government

Publication Information

PubMed ID
Public Release Type
Journal
Publication Year
2012
Affiliation
University of Pennsylvania, Philadelphia, PA, USA. rajender.reddy@uphs.upenn.edu
Authors
Afdhal N, Belle S, Belle SH, Borg E, Bowen J, Colagreco J, D'Amato M, Davis P, Doo E, Duffy L, Fried M, Fried MW, Gupta D, Hawke R, Hawke RL, Hoofnagle J, Howell M, Kaplan DE, Kennedy C, Kurs-Lasky M, Lawlor S, Meyers C, Meyers CM, Micheli A, Miller C, Navarro V, Navarro VJ, Reddy K, Reddy KR, Rovati L, Seeff L, Soule T, SyNCH Study Group, Thomas NP, Verma M, Wahed A, Wahed AS, Wirjosemito A, Zadorozny E
Studies
Citation
Reddy KR, Belle SH, Fried MW, Afdhal N, Navarro VJ, Hawke RL, Wahed AS, Doo E, Meyers CM, SyNCH Study Group. Rationale, challenges, and participants in a Phase II trial of a botanical product for chronic hepatitis C. Clin Trials 2012 Feb;9(1):102-12. Epub 2011 Nov 4.

Abstract

Chronic hepatitis C is associated with significant morbidity and mortality as a consequence of progression to cirrhosis, hepatocellular carcinoma, and liver failure. Current treatment for chronic hepatitis C with pegylated interferon (IFN) and ribavirin is associated with suboptimal responses and numerous adverse effects. A number of botanical products have been used to treat hepatic disorders. Silymarin, extracted from the milk thistle plant, Silybum marianum (L) Gaertn. (Asteraceae), has been most widely used for various liver disorders, including chronic hepatitis C, B, and alcoholic liver disease. However, the safety and efficacy of silymarin have not been studied systematically in chronic hepatitis C.