Esperion Reports Third Quarter 2022 Financial Results and Provides Company Update
Esperion (NASDAQ: ESPR) announced significant developments in its recent press release. The CLEAR Outcomes trial completed its last patient visit in October 2022, with topline results expected in January 2023 and full results in March at the American College of Cardiology event. In Q3 2022, U.S. net product revenue for NEXLETOL® and NEXLIZET® grew by 28% year-over-year to $14.0 million. Overall revenue for Q3 reached $19.0 million, reflecting a 32% increase versus 2021. However, the company reported a net loss of $55.1 million for the quarter.
- U.S. product revenue increased by 28% Y/Y to $14.0 million in Q3 2022.
- Total revenue rose by 32% in Q3 2022 compared to the same period last year.
- Significant reduction in selling, general, and administrative expenses by 36% Y/Y.
- Net loss of $55.1 million for Q3 2022, though improved from $69.4 million in Q3 2021.
- Overall revenue decreased by 10% for the nine months ended September 30, 2022, compared to 2021.
– CLEAR Outcomes Trial Achieved Last Patient Last Visit in October Ensuring Timely Trial Completion –
– Remain On Track to Report Topline Results in January 2023, with Full Results Targeted to be Presented in March at the American College of Cardiology 72nd Annual Scientific Sessions –
– U.S. Net Product Revenue of NEXLETOL® (bempedoic acid) Tablets and NEXLIZET® (bempedoic acid and ezetimibe) Tablets grew
– Will Showcase Pipeline Programs at R&D Day on November 9, 2022 –
ANN ARBOR, Mich., Nov. 01, 2022 (GLOBE NEWSWIRE) -- Esperion (NASDAQ: ESPR) today reported financial results for the third quarter ended September 30, 2022 and provided a business update.
“During the third quarter of 2022 our team has remained focused on closing out our unprecedented CLEAR Outcomes trial,” said Sheldon Koenig, President and Chief Executive Officer of Esperion. “We completed the last patient, last visit for the study in October and we remain on track to report topline results in January 2023, with comprehensive study results targeted to be presented at the American College of Cardiology 72nd Annual Scientific Sessions in March 2023. As we look ahead to what will be a transformational period for Esperion, we believe positive results will confirm the ability of bempedoic acid to lower cardiovascular risk and change the cardiovascular disease treatment landscape.”
Third Quarter 2022 Key Accomplishments and Recent Highlights
- Announced that bempedoic acid was recommended by the American College of Cardiology expert consensus decision pathway as an important oral non-statin for LDL-C (Low density lipoprotein cholesterol) lowering in ASCVD (atherosclerotic cardiovascular disease).
- Reduced selling, general and administrative expenses by
36% Year over Year while still delivering on our commitment to drive RPE growth (2.4% Quarter over Quarter). - Collaboration partner, Daiichi Sankyo Europe, announced new data presented at the European Society of Cardiology Congress in August 2022 from its multinational prospective, observational study, SANTORINI, demonstrating the persistent need among eligible patient populations to attain guideline-recommended LDL-C levels. Simulation study results further indicate that the addition of bempedoic acid on top of ezetimibe could result in significantly more patients achieving recommended LDL-C goals, potentially reducing their risk of cardiovascular events.
- Company hosting virtual R&D Day on November 9, 2022, to highlight pipeline programs featuring Global Scientific Leaders C. Michael Gibson, MS, MD (Harvard Medical Research Institutes) and Professor Peter Libby, MD (Brigham and Women’s Hospital and Harvard Medical School) who will discuss our investigational programs, including our landmark CLEAR Outcomes trial for bempedoic acid, oral PCSK9 inhibitor, and Next Generation ATP citrate lyase inhibition (ACLYi) platform in people suffering from cardiovascular, hepatorenal and metabolic diseases, as well as inflammation, and oncology.
- The CLEAR Path 1 Pediatric Clinical Trial began activating sites in August 2022. CLEAR Path 1 is a Phase 2 clinical trial investigating bempedoic acid in patients 6-17 years of age with heterozygous familial hypercholesterolemia (HeFH).
Third Quarter 2022 Financial Results
Total revenue for the third quarter ended September 30, 2022, was
U.S. product revenue for the third quarter ended September 30, 2022, was
Royalty revenue for the third quarter ended September 30, 2022, was
Research and development expenses for the third quarter ended September 30, 2022, were
Selling, general and administrative expenses for the third quarter ended September 30, 2022, were
Esperion had net losses of
As of September 30, 2022, cash, cash equivalents, restricted cash and investment securities available-for-sale totaled
Esperion ended the quarter with approximately 71.7 million shares of common stock outstanding, excluding the 2.0 million treasury shares to be purchased in the prepaid forward transaction as part of the convertible debt financing.
2022 Financial Outlook
The Company is reaffirming its prior operational expense guidance. Research and Development expenses for the full year 2022 are expected to be
Esperion expects full-year 2022 operating expenses to be approximately
Conference Call and Webcast Information
Esperion will host a webcast at 8:00 a.m. ET to discuss financial results and business progress. Please click here to pre-register to participate in the conference call and obtain your dial in number and PIN. You can also visit the Esperion website to listen to the call via live webcast. A recorded version will be available under the same link immediately following the conclusion of the conference call. Already registered? Access with your PIN here.
A live audio webcast can be accessed on the investors and media section of the Esperion website. Access to the webcast replay will be available approximately two hours after completion of the call and will be archived on the Company's website for approximately 90 days.
CLEAR Cardiovascular Outcomes Trial
CLEAR Outcomes is a Phase 3, event-driven, randomized, multicenter, double-blind, placebo-controlled trial designed to evaluate whether treatment with NEXLETOL reduces the risk of cardiovascular events in patients with or who are at high risk for cardiovascular disease with documented statin intolerance (inability to tolerate 2 or more statins, one at a low dose) and elevated LDL-C levels (fasting blood LDL-C ≥ 100 (2.6 mmol/L). The study, which includes over 14,000 patients at over 1,200 sites in 32 countries, accumulated the targeted 1,620 primary major adverse cardiovascular events (MACE-4) in August 2022.
Esperion Therapeutics
Esperion works hard to make our medicines easy to get, easy to take and easy to have. We discover, develop, and commercialize innovative medicines and combinations to lower cholesterol, especially for patients whose needs are not being met by the status quo. Our entrepreneurial team of industry leaders is inclusive, passionate, and resourceful. We are singularly focused on managing cholesterol so you can improve your health easily. For more information, please visit www.esperion.com and follow us on Twitter at www.twitter.com/EsperionInc.
Forward-Looking Statements
This press release contains forward-looking statements that are made pursuant to the safe harbor provisions of the federal securities laws, including statements regarding marketing strategy and commercialization plans, current and planned operational expenses, future operations, commercial products, clinical development, including the timing, designs and plans for the CLEAR Outcomes study and its results, plans for potential future product candidates, financial condition and outlook, including expected cash runway, and other statements containing the words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “suggest,” “target,” “potential,” “will,” “would,” “could,” “should,” “continue,” and similar expressions. Any express or implied statements contained in this press release that are not statements of historical fact may be deemed to be forward-looking statements. Forward-looking statements involve risks and uncertainties that could cause Esperion’s actual results to differ significantly from those projected, including, without limitation, the impact of the ongoing COVID-19 pandemic on our business, revenues, results of operations and financial condition, the net sales, profitability, and growth of Esperion’s commercial products, clinical activities and results, supply chain, commercial development and launch plans, and the risks detailed in Esperion’s filings with the Securities and Exchange Commission. Any forward-looking statements contained in this press release speak only as of the date hereof, and Esperion disclaims any obligation or undertaking to update or revise any forward-looking statements contained in this press release, other than to the extent required by law.
Contact:
Esperion Corporate Communications
corporateteam@esperion.com
Esperion Therapeutics, Inc.
Balance Sheet Data
(In thousands)
(Unaudited)
September 30, 2022 | December 31, 2021 | ||||||
Cash and cash equivalents | $ | 159,399 | $ | 208,892 | |||
Restricted cash | 50,000 | 50,000 | |||||
Investments | 29,942 | 50,441 | |||||
Working capital | 179,440 | 255,620 | |||||
Total assets | 312,827 | 381,590 | |||||
Revenue interest liability | 284,684 | 257,039 | |||||
Convertible notes, net of issuance costs | 259,487 | 258,280 | |||||
Common stock | 72 | 61 | |||||
Accumulated deficit | (1,284,549 | ) | (1,106,377 | ) | |||
Total stockholders' deficit | (294,100 | ) | (196,944 | ) | |||
Esperion Therapeutics, Inc.
Statement of Operations
(In thousands, except share and per share data)
(Unaudited)
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||
| 2022 | 2021 | 2022 | 2021 | |||||||||||
Revenues: | | | |||||||||||||
Product sales, net | $ | 13,964 | $ | 10,895 | $ | 40,896 | $ | 27,855 | |||||||
Collaboration revenue | 5,016 | 3,514 | 15,761 | 35,191 | |||||||||||
Total Revenues | 18,980 | 14,409 | 56,657 | 63,046 | |||||||||||
| |||||||||||||||
Operating expenses: | |||||||||||||||
Cost of goods sold | 6,506 | 5,558 | 22,807 | 9,142 | |||||||||||
Research and development | 29,143 | 25,331 | 85,894 | 78,359 | |||||||||||
Selling, general and administrative | 24,954 | 39,265 | 84,944 | 146,647 | |||||||||||
Total operating expenses | 60,603 | 70,154 | 193,645 | 234,148 | |||||||||||
| |||||||||||||||
Loss from operations | (41,623 | ) | (55,745 | ) | (136,988 | ) | (171,102 | ) | |||||||
| |||||||||||||||
Interest expense | (14,153 | ) | (13,654 | ) | (42,481 | ) | (32,923 | ) | |||||||
Other income, net | 659 | 13 | 1,297 | 36 | |||||||||||
Net loss | $ | (55,117 | ) | $ | (69,386 | ) | $ | (178,172 | ) | $ | (203,989 | ) | |||
| |||||||||||||||
Net loss per common share – basic and diluted | $ | (0.81 | ) | $ | (2.62 | ) | $ | (2.78 | ) | $ | (7.78 | ) | |||
| |||||||||||||||
Weighted-average shares outstanding – basic and diluted | 67,806,292 | 26,455,209 | 64,021,248 | 26,225,730 |
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