Pegylated Interferon Alfa-2a Monotherapy Efficacious in Treating Dialysis Patients With Hepatitis C: Presented at AASLD
Unregistered User
If this is not your name, click here.
Contact Us | Order Now | Journals | Bookstore | Register a colleague
 
  SEARCH  
News
Bookstore
Medline
The Web
Meetings & Congresses
Complete Doctor's Guide
 


 EXPLORE :
 news  All News
 webcasts All Webcasts
 All cases All Cases
 Meetings All Meetings & Congresses
 Medical All Medical Resources

top





New drugs / indications

English Dictionary

Medical Dictionary

Thesaurus



Warning | Privacy | Awards



 Favourite Journals 

Click here to choose your favourite journals


 Favourite Sites 

Click here to choose your favourite sites


 Languages 



  




Pegylated Interferon Alfa-2a Monotherapy Efficacious in Treating Dialysis Patients With Hepatitis C: Presented at AASLD

By Maria Bishop

BOSTON, MA -- November 5, 2007 -- Pegylated interferon (PEG-IFN) alfa-2a monotherapy is effective in dialysis patients with hepatitis C virus (HCV), demonstrating a sustained virological response (SVR) of 36.8% in this hepatologically compromised patient population, researchers reported here at the 58th Annual Scientific Meeting of the American Association for the Study of Liver Disease (AASLD).

PEG IFN alfa-2a, due to its limited excretion (< 10%) appears to be the preferred treatment of haemodialysis patients, despite serious side effects, noted lead author Reinhart Zachoval, MD, Head of Ambulatory Hepatological Care, Medical Clinic 2, Ludwig - Maximilians University (LMU), Grosshadern, Munich, Germany.

Dr. Zachoval led an open, prospective multicentre study of 38 haemodialysis patients (23 male) with chronic hepatitis C to evaluate the rate of SVR after 48 weeks of PEG-IFN alfa-2a monotherapy. Patients received 135 ug of PEF-IFN alfa-2a per week at the end of their dialysis procedures for 24 weeks. If patients achieved a decline of HCV ribonucleic acid (RNA) greater than 2 log, therapy was continued for a total of 48 weeks.

In a subgroup of 11 patients, results from a dose of 180 ug of the therapy were recorded.

SVR was observed in 14 of the 38 patients (36.8%). Seventeen patients were non-responders, and 7 patients showed a relapse of viremia.

Repeated dosing at both dose levels resulted in constant drug levels in patients undergoing haemodialysis.

A high rate of severe side effects was also shown, however, and 8 patients discontinued the trial due to serious adverse events, including death (myocardial infarction), massive retinal arterial embolisation, grand mal seizures, instable angina, pneumonia, and massive diabetic foot syndrome.

While the drug demonstrated good efficacy, the high rate of side effects in this study therefore necessitates meticulous patient selection in these often comorbid individuals, concluded Dr. Zachoval.

This trial was sponsored by Roche Pharma, Grenzach, Germany.

[Presentation title: PEG-IFN alfa-2a Monotherapy in Dialysis Patients Infected With HCV. Abstract 328]

E-mail this page
to a friend or colleague!
To print,
use this version




Any question regarding a medical diagnosis, treatment, referral, drug availability or pricing should be directed to either a licensed physician or to the product's manufacturer.

If you have any technical questions or other concerns about this site, feel free to contact us at webmaster@docguide.com.

All contents Copyright (c) 1995- Doctor's Guide Publishing Limited. All rights reserved.


Employment opportunities | Partnering opportunities