Eiger BioPharmaceuticals Announces Complete Enrollment of D-LIVR, the Largest Phase 3 Study in Hepatitis Delta Virus (HDV), Investigating Lonafarnib, the Only Oral Agent in Development for HDV
Eiger BioPharmaceuticals announced the completion of enrollment in the Phase 3 D-LIVR study, which examines Lonafarnib for chronic hepatitis delta virus (HDV) infection. This trial, the largest of its kind with 400+ patients across 116 sites in 22 countries, aims to compare two treatment regimens against a placebo. The results are crucial for potential U.S. and European approvals. Topline data is expected by the end of 2022, marking a significant milestone for Eiger and offering hope for improved treatment options for HDV patients.
- Completion of enrollment in the largest Phase 3 HDV study with over 400 patients.
- Topline data release planned for end of 2022, potentially supporting regulatory approval.
- Lonafarnib has Orphan Drug and Fast Track designations, enhancing its market potential.
- The trial results are still pending, introducing uncertainty until data is released.
PALO ALTO, Calif., Nov. 1, 2021 /PRNewswire/ -- Eiger BioPharmaceuticals, Inc. (Nasdaq:EIGR), a commercial-stage biopharmaceutical company focused on the development and commercialization of targeted therapies for serious rare and ultra-rare diseases, today announced completion of enrollment in the Phase 3 D-LIVR study evaluating two different treatment regimens containing Lonafarnib, the Company's first-in-class oral prenylation inhibitor, for the treatment of chronic hepatitis delta virus (HDV) infection. The two regimens include all-oral Lonafarnib boosted with ritonavir and in combination with peginterferon alfa.
The D-LIVR study spans 116 clinical sites across 22 countries and is the largest Phase 3 study ever conducted in HDV. Over 400 patients have now been enrolled in D-LIVR. Eiger is planning for topline data release by the end of 2022.
"Completing enrollment of D-LIVR is a major milestone for both Eiger and patients with chronic HDV infection," said David Cory, President and CEO. "This trial is expected to generate pivotal results that will support approval of two Lonafarnib-based regimens for HDV in the U.S., Europe, and rest of world. In addition, D-LIVR is generating the single, largest source of HDV patient data from a well-controlled, global Phase 3 study to better characterize and understand this devastating disease. We look forward to reporting data from this landmark study and bringing potential new treatment options to patients."
About D-LIVR
D-LIVR (Delta Liver Improvement and Virologic Response in HDV) is a global, multi-center, Phase 3 study to evaluate two Lonafarnib-based regimens: an all-oral arm of Lonafarnib boosted with ritonavir and a combination arm of Lonafarnib boosted with ritonavir combined with peginterferon alfa, with each arm to be compared to a placebo arm, in HDV-infected patients. The study also includes a peginterferon alfa monotherapy arm which will be used to demonstrate contribution of effect only. The Lonafarnib containing arms will not be required to demonstrate superiority over peginterferon alfa. The primary endpoint is a composite of ≥ 2 log decline in HDV RNA and ALT normalization at end of 48 weeks of treatment. Key secondary endpoints include histologic improvement and improvement in fibrosis after 48 weeks of treatment, based on biopsies conducted at the start and end of treatment for all patients.
About Hepatitis Delta Virus (HDV)
HDV is the most severe form of human viral hepatitis. HDV occurs only as a co-infection in individuals infected with hepatitis B virus (HBV). HDV leads to more severe liver disease than HBV alone and is associated with accelerated liver fibrosis, liver cancer, and liver failure. It is estimated that
HDV is a disease with a significant impact on global health, which may affect up to 15-20 million people worldwide. Globally, HDV infection is reported to be present in approximately
About Lonafarnib
Lonafarnib is a well-characterized, first-in-class, oral prenylation inhibitor which blocks the final step in HDV viral assembly. Lonafarnib has been dosed in over 450 HDV-infected patients across global clinical sites, including the fully enrolled Phase 3 D-LIVR study. Lonafarnib has been granted Orphan Drug designation by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA), Fast Track designation and Breakthrough designation by FDA and PRIME designation by EMA. Eiger licensed exclusive worldwide rights to lonafarnib from Merck, known as MSD outside of the United States and Canada.
About Eiger
Eiger is a commercial-stage biopharmaceutical company focused on the development and commercialization of targeted therapies for serious rare and ultra-rare diseases.
Eiger's lead clinical programs are focused on the development of foundational therapies for HDV infection, the most serious form of viral hepatitis, with two complementary HDV treatments. Lonafarnib is a first-in-class, oral prenylation inhibitor and Peginterferon Lambda is a first-in-class, type III, well-tolerated interferon. Both Lonafarnib and Peginterferon Lambda are in global Phase 3 studies.
For additional information about Eiger and its clinical programs, please visit www.eigerbio.com.
Forward Looking Statements
This press release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements other than statements of historical facts, including statements regarding our future financial condition, timing for and outcomes of clinical results, business strategy and plans and objectives for future operations, are forward-looking statements. These forward-looking statements include words such as "will," "may," "continue," "plan," "expect," "could," "potentially," other words of similar meaning and the negative of these terms. Forward-looking statements are our current statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things, the potential of a Lonafarnib-based regimen to be an effective therapy for HDV, the timely generation of clinical trial data to support a New Drug Application and its submission for approval to the FDA and a Marketing Authorization Application and its submission for approval to the EMA. Various important factors could cause actual results or events to differ materially from the forward-looking statements that Eiger makes, including additional applicable risks and uncertainties described in the "Risk Factors" sections in the Quarterly Report on Form 10-Q for the quarter ended June 30, 2021 and Eiger's subsequent filings with the SEC. The forward-looking statements contained in this press release are based on information currently available to Eiger and speak only as of the date on which they are made. Eiger does not undertake and specifically disclaims any obligation to update any forward-looking statements, whether as a result of any new information, future events, changed circumstances or otherwise.
Investors and Media:
Sri Ryali – CFO
Email: sryali@eigerbio.com
Phone: 1-650-272-6138
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FAQ
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