Anadys
Initiates Dosing in Phase IIb Study of ANA598
San
Diego -- January 26, 2011 -- Anadys Pharmaceuticals, Inc. (Nasdaq:
ANDS) announced today that dosing has begun in the Phase IIb
study of ANA598 in combination with pegylated interferon and
ribavirin in hepatitis C patients. ANA598, the Company's direct-acting
antiviral, is being tested in both treatment-naive patients
and patients who failed a prior course of HCV therapy with interferon
and ribavirin. Approximately 275 patients are expected to be
enrolled in the study. The primary endpoint of the study is
Sustained Virological Response 24 weeks after patients complete
treatment, known as SVR24.
The company expects to receive Week 8 antiviral response data
for treatment-naive patients by the end of the second quarter
of 2011, Week 12 antiviral response data for treatment-experienced
patients in the third quarter of 2011 and Week 24 antiviral
response data for both groups in the fourth quarter of 2011.
About Anadys
Anadys
Pharmaceuticals, Inc. is a biopharmaceutical company dedicated
to improving patient care by developing novel medicines for
the treatment of hepatitis C. The company believes hepatitis
C represents a large unmet medical need in which meaningful
improvements in treatment outcomes may be attainable with the
introduction of new medicines. Anadys is conducting a Phase
IIb study of ANA598, the company's DAA, added to current standard
of care for the treatment of hepatitis C. The company is also
preparing to resume clinical development of ANA773, the company's
oral, small-molecule inducer of endogenous interferons that
acts via the Toll like receptor 7, or TLR7, pathway in hepatitis
C.
2/1/11
Source
Anadys
Pharmaceuticals. Anadys Initiates Dosing in Phase IIb Study
of ANA598. Press release. January 26, 2011.
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