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 reported its first quarter 2021 financial results and provided a business update.
“The Phase 3 D-LIVR study is now 75% enrolled, and by year-end we expect to complete enrollment of this landmark global study advancing Lonafarnib, the only oral agent in development for HDV, setting the stage for Week 48 end of treatment data in 2022,” said David Cory, President and CEO of Eiger. “In parallel, we will initiate the Phase 3 LIMT-2 study in 2021 to advance Lambda, a well-tolerated interferon, also toward registration for HDV. Most recently, with a goal of developing a convenient, outpatient treatment for COVID-19, we announced that a Lambda arm will be included in the ongoing, multi-center, Phase 3 TOGETHER platform study in Brazil.”
Program Updates and Upcoming Milestones
Lonafarnib for HDV
- First and only oral therapy in clinical development for HDV
- Phase 3 D-LIVR study is the largest and only global HDV study
- Study is 75% enrolled, including patients randomized to date and patients in screening that are expected to be randomized
- Full enrollment of 400 patients expected by end of 2021
Peginterferon Lambda (Lambda) for HDV
- Well-tolerated interferon for convenient once weekly subcutaneous injection
- Phase 3 LIMT-2 study (N=150) expected to initiate in the second half of 2021
Zokinvy® (lonafarnib) for Progeria
- U.S. commercial launch in January 2021
- EMA approval expected by end of 2021
Lambda for COVID-19
- U.S. IND now open and includes Phase 2/3 study protocol
- Lambda to be included in ongoing Phase 3 TOGETHER platform study
- Recruiting at 11 sites in Brazil with plans to add a site in Toronto, Canada
- Lambda arm will include up to 800 high-risk, non-hospitalized patients
- Endpoints align with FDA Guidance for COVID-19 therapeutics
Avexitide for Post-Bariatric Hypoglycemia (PBH) and Congenital Hyperinsulinism (CHI)
- Advancing manufacturing, device, clinical and regulatory activities in 2021
- Registration-enabling studies for PBH and CHI could begin in 2022
- Appointed Kim Sablich, Industry Veteran, to Board of Directors in April 2021
- Cash, cash equivalents and investments of $160.5 million at the end of first quarter 2021 expected to fund planned operations into fourth quarter 2023
First Quarter 2021 Financial Results
Eiger reported total net revenue of $3.6 million from Zokinvy product sales for first quarter 2021. Zokinvy launched commercially in the U.S. in January 2021 with first quarter sales including inventory stocking at the specialty pharmacy.
Research and Development expenses were $13.8 million for first quarter 2021 as compared to $9.5 million for the same period in 2020. The increase was primarily due to clinical trial related expenses, including contract manufacturing, and headcount related expenses, including stock-based compensation expense. The increase was partially offset by lower expenses for regulatory consulting services.
Selling, General and Administrative expenses were $5.6 million for first quarter 2021, as compared to $5.2 million for the same period in 2020. The increase in first quarter 2021 was primarily due to outside consulting and advisory services.
Total operating expenses include non-cash expenses of $2.2 million for first quarter 2021, as compared to $2.0 million same period in 2020.
Eiger reported first quarter 2021 net income of $29.2 million, or $0.85 on a fully-diluted per share basis. This compares to a net loss of $15.2 million, or $0.62 on a per share basis, for first quarter 2020. First quarter 2021 net income was driven by a one-time gain from the sale of the Zokinvy Priority Review Voucher (PRV). The company reported $45.9 million as Other Income, Net, which primarily reflects net PRV sale proceeds.
Cash, cash equivalents, and investments as of March 31, 2021 totaled $160.5 million compared to $128.8 million on December 31, 2020.
As of March 31, 2021, the company had 34.0 million of common shares outstanding.
At 4:30 p.m. Eastern Time today, Eiger will host a conference call to discuss its financial results and provide a business update. The live and replayed webcast of the call will be available through the company’s website at www.eigerbio.com. To participate in the live call by phone, dial (844) 743-2495 (U.S.) or (661) 378-9529 (International) and enter conference ID 1090136. The webcast will be archived and available for replay for at least 90 days after the event.
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 Hepatitis Delta Virus (HDV) infection, the most serious form of viral hepatitis, with two complementary HDV treatments. Lonafarnib is a first-in-class, oral prenylation inhibitor in a global Phase 3 trial. Peginterferon lambda is a first-in-class, well-tolerated type III interferon entering Phase 3.
Zokinvy® for the treatment of Hutchinson-Gilford Progeria Syndrome (HGPS or Progeria) and processing-deficient progeroid laminopathies is the Company’s first FDA approved product. A Marketing Authorization Application (MAA) is under review by the European Medicines Agency (EMA).
For additional information about Eiger and its clinical programs, please visit www.eigerbio.com.
Note Regarding Forward-Looking Statements
This press release contains “forward-looking” statements that involve substantial risks and uncertainties. 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 terminology such as “believe,” “will,” “may,” “estimate,” “continue,” “anticipate,” “contemplate,” “intend,” “target,” “project,” “should,” “plan,” “expect,” “predict,” “could,” “potentially” or 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, our anticipated significant milestones in 2021; the timing of our ongoing and planned clinical development; the sufficiency of our cash, cash equivalents and investments to fund our operations into the fourth quarter of 2023; our development programs for Zokinvy generally; and the potential approval of Zokinvy in jurisdictions outside of the U.S., including the EU; our progression and continued enrollment of our Phase 3 D-LIVR study in HDV; our ability to maintain supply of our commercial and clinical trial materials; our plans to advance Lambda in HDV in the U.S. and EU; our progression of Lambda for COVID-19 and Avexitide for PBH and CHI; our ability to finance the continued advancement of our development pipeline products; and the potential for success of any of our product candidates. These statements concern product candidates that have not yet been approved for marketing by the U.S. Food and Drug Administration (FDA). No representation is made as to their safety or effectiveness for the purposes for which they are being investigated. 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 March 31, 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.
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|Eiger BioPharmaceuticals Inc.|
|Condensed Consolidated Balance Sheets|
|Three Months Ended||Year Ended|
|March 31||December 31,|
|Cash and cash equivalents||$ 108,410||$ 28,864|
|Debt securities, available-for-sale||52,082||99,976|
|Prepaid expenses and other current assets||7,358||8,873|
|Total current assets||169,886||137,806|
|Property and equipment, net||659||709|
|Operating lease right-of-use assets||1,049||1,176|
|Total assets||$ 175,515||$ 143,594|
|LIABILITIES AND STOCKHOLDERS’ EQUITY|
|Current liabilities||$ 17,517||$ 16,627|
|Total liabilities and stockholders’ equity||$ 175,515||$ 143,594|
|(1) Derived from the audited financial statements, included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2020.|
|Eiger BioPharmaceuticals Inc.|
|Condensed Consolidated Statements of Operations Financial Data|
|(in thousands, except per share and share amounts)|
|Three Months Ended|
|Product revenue, net||$ 3,646||$ –|
|Costs and operating expenses:|
|Costs of sales||53||–|
|Research and development(1)||13,842||9,481|
|Selling, general and administrative(1)||5,564||5,241|
|Total costs and operating expenses||19,459||14,722|
|Loss from operations||(15,813)||(14,722)|
|Other income, net||45,914||–|
|Income before provision for income taxes||29,267||(15,239)|
|Provision for income taxes||19||—|
|Net income (loss)||$ 29,248||$ (15,239)|
|Net income (loss) per common share:|
|Basic||$ 0.86||$ (0.62)|
|Diluted||$ 0.85||$ (0.62)|
|Weighted-average common shares outstanding:|
|(1)||Includes stock-based compensation expense of:|
|Three Months Ended|
|Research and development||$ 391||$ 389|
|Selling, general and administrative||1,158||1,240|
|Total stock-based compensation expense||$ 1,549||$ 1,629|
SOURCE Eiger BioPharmaceuticals, Inc.