Investor Update
Basel, 2 November 2007
Roche’s
Oral Polymerase Inhibitor Shows Robust Antiviral Efficacy in Treatment of Chronic Hepatitis C
Roche
progresses R1626 into phase IIb study called POLI 1
R1626, one of Roche’s
new investigational drugs for hepatitis C (HCV), has shown promising antiviral efficacy when given in
combination with PEGASYS (peginterferon alfa-2a (40KD)) and COPEGUS (ribavirin), according to results
being presented at the American Association for the Study of the Liver (AASLD) meeting in Boston.1
After
4 weeks of treatment with the triple combination, the hepatitis C virus could no longer be detected
in up to 81% of the HCV-infected patients. Patients receiving the triple combination had a mean decrease
in viral load of 5.2 log10 from baseline, indicating a robust and rapid virological response.
R1626
belongs to a class of antivirals called polymerase inhibitors, which are being investigated in combination
with the current standard of care, pegylated interferon and ribavirin. The hope is that this potent
combination will increase the number of patients who manage to clear the hepatitis C virus from their
system and become cured of this disease.
Lack of Resistance
Demonstrated
R1626
has also demonstrated a high barrier to the development of resistance, according to a second abstract
being presented at the conference.2 Resistance to R1626 was not identified
following intensive testing
for either 2 weeks of treatment with R1626 as monotherapy or for 4 weeks in patients treated with R1626
in combination with the standard of care.
“The results from this phase
IIa study show that R1626 has a profound effect when used in combination with PEGASYS plus COPEGUS,”
said Dr Paul Pockros (Scripps Clinic, San Diego, California), the lead investigator of the study. “The
synergistic antiviral effect of R1626 along with the lack of resistance means that R1626 could be an
exciting antiviral treatment option for patients with hepatitis C if a safe and acceptable dosage regimen
can be determined in future studies.”
The study found1:
- Up to 81% of patients treated with R1626 1500 mg BID + PEGASYS + ribavirin had an undetectable HCV viral load by week 4 (mean reduction of 5.2 log10 IU/ml)
- ALT, a liver enzyme, normalised in approximately 50% of patients in R1626 treatment groups
- Most reported adverse events were mild to moderate. A higher incidence of grade 4 neutropaenia was reported in R1626 treatment arms (ie, 39% of patients receiving the R1626 1500 mg dose in combination with PEGASYS and ribavirin), and it was the main reason for dose reductions and discontinuations
Further
phase II studies are underway to investigate R1626 in combination with PEGASYS plus COPEGUS.
Start
of the Phase IIb Trial
As a result of the robust antiviral effect seen in the phase
IIa
study, R1626 is being progressed into a phase IIb study to further investigate new treatment regimens,
in combination with a standard or lower dose of PEGASYS plus a standard dose of COPEGUS. This phase
IIb trial, called POLI 1, is now open and about to enroll patients in eight countries – Austria, Australia,
Canada, France, Germany, Italy, Spain and the US. More information about R1626 and these clinical studies
can be found on www.roche-trials.com.
"The strong
synergistic antiviral
effect seen among R1626, PEGASYS and COPEGUS in the Phase IIa study together with the design of the
phase IIb study makes me confident that we will find the right balance between the safety and efficacy,"
said Dr. Stefan Zeuzem, Professor of Medicine at J.W. Goethe University Hospital, Frankfurt, Germany,
and a lead investigator in this Phase IIb study.
About
Hepatitis C
Hepatitis
C, the most common chronic blood-borne infection, is transmitted primarily through blood or blood products.
Hepatitis C chronically infects 180 million people worldwide, with an additional three to four million
people newly infected each year.3 It is a leading cause of cirrhosis, liver
cancer and liver failure,
despite being potentially curable. The future of hepatitis C therapy is likely to involve combinations
of new small-molecule antiviral drugs and pegylated interferon-based treatment, like PEGASYS.
About
Roche
Headquartered in Basel, Switzerland, Roche is one of the world’s leading
research-focused
healthcare groups in the fields of pharmaceuticals and diagnostics. As the world’s largest biotech company
and an innovator of products and services for the early detection, prevention, diagnosis and treatment
of diseases, the Group contributes on a broad range of fronts to improving people’s health and quality
of life. Roche is the world leader in in-vitro diagnostics and drugs for cancer and transplantation,
is a market leader in virology and is active in other major therapeutic areas such as autoimmune diseases,
inflammation, metabolic disorders and diseases of the central nervous system. In 2006, sales by the
Pharmaceuticals Division totalled 33.3 billion Swiss francs, and the Diagnostics Division posted sales
of 8.7 billion Swiss francs. Roche has R&D agreements and strategic alliances with numerous partners,
including majority ownership interests in Genentech and Chugai, and invests approximately 7 billion
Swiss francs a year in R&D. Worldwide, the Group employs about 75,000 people. Additional information
is available on the Internet at www.roche.com.
All
trademarks used or
mentioned in this release are protected by law.
References:
1.
Pockros P. Robust synergistic antiviral effect of R1626 in combination with Peginterferon alfa-2a (40KD),
with or without ribavirin – interim analysis results of phase 2a sudy. In: 58th Annual Meeting of the
American Association for the Study of Liver Diseases; 2007 November 2-6; Boston, USA; 2007.
2.
Le Pogam S. A high barrier to resistance may contribute to the robust antiviral effect demonstrated
by R1626 in HCV genotype 1-infected treatment-naive patients. In: 58th Annual Meeting of the American
Association for the Study of Liver Diseases; 2007 November 2-6, 2007; Boston, USA; 2007.
3.
World Health Organization. Initiative for Vaccine Research, Viral Cancers, Hepatitis C. 2006. (Accessed
July 24, 2006, at http://www.who.int/vaccine_research/diseases/viral_cancers/en/index2.html)