Eiger BioPharmaceuticals Announces Abstracts and Presentations of Lonafarnib Data in Hepatitis Delta (HDV) at the European Association for the Study of the Liver Conference - April 22 to 26, 2015
13 Apr, 2015, 08:00 ET
PALO ALTO, Calif., April 13, 2015 /CNW/ -- Eiger BioPharmaceuticals Incorporated, today announced that abstracts from its Hepatitis Delta Virus (HDV) development program will be presented at the European Association for the Study of the Liver (EASL) in Vienna, Austria, April 22 to 26, 2015. Data from the Phase 2 study of lonafarnib boosted with ritonavir in patients infected with HDV will be presented for the first time. The accepted abstracts, related invited talks and symposium sessions are listed below and are now available online.
Lonafarnib Abstracts, Posters and Oral Presentations at EASL
- "Understanding hepatitis delta virus and HBsAg kinetics during treatment with prenylation inhibitor lonafarnib via mathematical modeling." Abstract/ePoster LP36; April 23-25, 2015, Hall B.
- "Optimizing the prenylation inhibitor lonafarnib using ritonavir boosting in patients with chronic delta hepatitis."Abstract 0118; Oral presentation on April 25, 2015 at 1:00 P.M. CEST, Strauss 3.
- "Optimizing the prenylation inhibitor lonafarnib using ritonavir boosting in patients with chronic delta hepatitis" will be delivered as an invited talk at the 9th meeting of the Hepatitis Delta International Network (HDIN) on April 22, 2015 at 2 P.M. CEST, Room Schubert 6.
Lonafarnib is a well-characterized, late stage, orally active agent targeting farnesyltransferase, an enzyme involved in modification of proteins through a process called prenylation. HDV uses this host cellular process inside liver cells to complete a key step in its life cycle. Lonafarnib inhibits the prenylation step of HDV replication inside liver cells and blocks the ability of the virus to multiply. Since prenylation is carried out by a host enzyme there is also a theoretical higher barrier to develop viral resistance mutations with lonafarnib therapy.
Lonafarnib is an investigational product and its safety and efficacy have not yet been established for any indication.
Hepatitis Delta is caused by infection with the hepatitis D virus (HDV) and is considered to be the most severe form of viral hepatitis in humans. Hepatitis D occurs only as a co-infection in individuals with hepatitis B (HBV), leads to more severe liver disease than HBV alone, and is associated with accelerated liver fibrosis, liver cancer, and liver failure. HDV is a disease with a significant impact on global health affecting ~15 million people worldwide. The prevalence of HDV varies between different parts of the world. Globally, HDV infection is reported to be 5-6% of chronic hepatitis B carriers. Lonafarnib has been granted the Orphan Drug Designation by the US FDA and the European Medicines Agency (EMA). In some parts of the world, including certain areas of China, Russia, Central Asia, Turkey, Africa, and South America, prevalence as high as 40% has been reported in HBV infected patients.
Eiger is a privately held biotechnology company focused on the research, development and commercialization of innovative therapies in viral hepatitis. The company is focused on developing lonafarnib for the treatment of Hepatitis Delta Virus (HDV), the most severe form of viral hepatitis. Lonafarnib is not approved for any indication. Eiger's research programs are focused on the discovery of targeted, small-molecule therapeutics and biomarkers to treat and monitor serious liver diseases. For additional information about Eiger and its R&D pipeline, please visit www.eigerbio.com.
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Investors: Jim Shaffer, Eiger BioPharmaceuticals, Inc., 919-345-4256, [email protected]
SOURCE Eiger BioPharmaceuticals, Inc.
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