Российское сообщество больных Гепатитом С
 

3.1.1g Roferon INTERFERON ALPHA 2A, RECOMBINANT

In studies in which Roferon-A was administered three times a week for 12 months 12% of the patients experienced a sustained response to therapy. Of these patients, 9% maintained this sustained response during continuous follow-up for up to four years.

Roferon, produced by Hoffman-LaRoche, has US FDA approval for use as treatment for hepatitis C since 1996. It has been modified to produce Pegasys, an improved “time-release” treatment that is injected once a week. (See Part III.1.2).

Roferon may be effective in non-responders to other interferon products.



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