Full Press Release Details
Altimmune Reports Fourth Quarter and Full Year 2021 Financial Results and Provides a Corporate Update
Data readouts from multiple clinical trials expected during the next 6 to 12 months
Strong cash position of $190.3 million as of December 31, 2021
GAITHERSBURG, MD, -- March 15, 2022 -- Altimmune, Inc. (Nasdaq: ALT), a clinical-stage biopharmaceutical company, today announced financial results for the fourth quarter and full year ended December 31, 2021 and provided a corporate update.
"We expect the next 12 months to be a period of intense execution with value-creating data readouts from multiple clinical trials. We are extremely pleased with the progress of our pemvidutide (ALT-801) program as we showed double-digit weight loss after 12 weeks of treatment, good tolerability without the use of dose titration, and pronounced decreases in serum lipids commonly associated with cardiovascular disease. We also observed a remarkable reduction in liver fat content to undetectable levels after only 6 weeks of pemvidutide treatment in subjects with hepatic steatosis, or fatty liver," said Vipin K. Garg, Ph.D., President and Chief Executive Officer at Altimmune. "In addition to our ongoing 12-week Phase 1b NAFLD trial, we expect to initiate a 48-week Phase 2 trial of pemvidutide in obesity, the MOMENTUM trial, in the next few weeks and look forward to sharing data from both of these trials later this year. In addition, we expect to read out our HepTcell trial in the first half of 2023."
Recent Highlights and Anticipated Milestones:
Pemvidutide1 (ALT-801)
Financial Results for the Three Months Ended December 31, 2021
Conference Call Information
| Date: | Tuesday, March 15 |
| Time: | 8:30 am Eastern Time |
| Domestic Dial-in: | (844) 615-6509 |
| International Dial-in: | (918) 922-3148 |
| Conference ID: | 4557398 |
| Webcast: | https://edge.media-server.com/mmc/p/5www3cgz |
Following the conclusion of the call, the webcast will be available for replay on the Investor Relations page of the Company's website at www.altimmune.com. The Company has used, and intends to continue to use, the IR portion of its website as a means of disclosing material non-public information and for complying with disclosure obligations under Regulation FD.
Pemvidutide is a novel, investigational, peptide-based GLP-1/glucagon dual receptor agonist in development for the treatment of obesity and NASH. Activation of the GLP-1 and glucagon receptors is believed to mimic the complementary effects of diet and exercise on weight loss, with GLP-1 suppressing appetite and glucagon increasing energy expenditure. By combining GLP-1 and glucagon activity in a single peptide, pemvidutide has the potential to achieve weight loss comparable to bariatric surgery. Pemvidutide incorporates the EuPortTM domain, a proprietary technology that increases its serum half-life for weekly dosing while slowing the entry of pemvidutide into the bloodstream, which may improve its tolerability. In a 12-week Phase 1 clinical trial, pemvidutide-treated subjects demonstrated striking reductions in body weight, liver fat and serum lipids commonly associated with cardiovascular disease.
HepTcell is a novel, investigational, immunotherapeutic comprised of nine synthetic peptides representing conserved hepatitis B (HBV) sequences formulated with IC31 , a TLR9-based adjuvant from Valneva SE. The HBV-directed peptides are designed to drive T cell responses against all HBV genotypes towards a functional cure for chronic HBV in patients of diverse genetic backgrounds.
Altimmune is a clinical-stage biopharmaceutical company focused on the development of novel peptide-based therapeutics for the treatment of obesity and liver diseases. The company's lead product candidate, pemvidutide, is a GLP-1/glucagon dual receptor agonist that is being developed for the treatment of obesity and NASH. In addition, Altimmune is developing HepTcell , an immunotherapeutic designed to achieve a functional cure for chronic hepatitis B. For more information, please visit www.altimmune.com.
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Forward-Looking Statement
Any statements made in this press release relating to future financial or business performance, conditions, plans, prospects, trends, or strategies and other financial and business matters, including without limitation, the timing of key milestones for our clinical assets, the initiation and timing of the Phase 2 clinical trial of pemvidutide, the timing of the data readouts for the Phase 2 clinical trial of pemvidutide, and the prospects for regulatory approval, commercializing or selling any product or drug candidates, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. In addition, when or if used in this press release, the words "may," "could," "should," "anticipate," "believe," "estimate," "expect," "intend," "plan," "predict" and similar expressions and their variants, as they relate to Altimmune, Inc. (the "Company") may identify forward-looking statements. The Company cautions that these forward-looking statements are subject to numerous assumptions, risks, and uncertainties, which change over time. Important factors that may cause actual results to differ materially from the results discussed in the forward looking statements or historical experience include risks and uncertainties, including risks relating to: potential impacts due to crises, including conflicts and wars (like the ongoing conflict in Ukraine) and pandemics (like the COVID-19 pandemic), such as delays in regulatory review, manufacturing and supply chain interruptions, access to clinical sites, enrollment, adverse effects on healthcare systems and disruption of the global economy; the reliability of the results of studies relating to human safety and possible adverse effects resulting from the administration of the Company's product candidates; the Company's ability to manufacture clinical trial materials on the timelines anticipated; and the success of future product advancements, including the success of future clinical trials. Further information on the factors and risks that could affect the Company's business, financial conditions and results of operations are contained in the Company's filings with the U.S. Securities and Exchange Commission, including under the heading "Risk Factors" in the Company's annual report on Form 10-K for the fiscal year ended December 31, 2021 filed with the SEC, which is available at www.sec.gov.
Investor & Media Contacts:
| Rich Eisenstadt |
| Chief Financial Officer |
| Phone: 240-654-1450 |
| reisenstadt@altimmune.com |
CONSOLIDATED BALANCE SHEETS
| December 31, | ||||||
| 2021 | 2020 | |||||
| ASSETS | ||||||
| Current assets: | ||||||
| Cash and cash equivalents | $ | 190,300,776 | $ | 115,917,807 | ||
| Restricted cash | 34,174 | 34,174 | ||||
| Total cash, cash equivalents and restricted cash | 190,334,950 | 115,951,981 | ||||
| Short-term investments | - | 100,005,558 | ||||
| Accounts receivable | 428,836 | 4,610,202 | ||||
| Income tax and R&D incentive receivables | 5,409,639 | 7,762,793 | ||||
| Prepaid expenses and other current assets | 7,952,690 | 1,926,675 | ||||
| Total current assets | 204,126,115 | 230,257,209 | ||||
| Property and equipment, net | 1,447,786 | 1,056,920 | ||||
| Intangible assets, net | 12,418,967 | 12,823,846 | ||||
| Other assets | 871,976 | 977,238 | ||||
| Total assets | $ | 218,864,844 | $ | 245,115,213 | ||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||
| Current liabilities: | ||||||
| Accounts payable | $ | 2,034,493 | $ | 612,293 | ||
| Contingent consideration | 6,090,000 | - | ||||
| Accrued expenses and other current liabilities | 10,151,437 | 11,408,154 | ||||
| Total current liabilities | 18,275,930 | 12,020,447 | ||||
| Contingent consideration | - | 5,390,000 | ||||
| Other long-term liabilities | 1,454,203 | 1,828,443 | ||||
| Total liabilities | 19,730,133 | 19,238,890 | ||||
| Commitments and contingencies (Note 17) | ||||||
| Stockholders' equity: | ||||||
| Common stock, $0.0001 par value; 200,000,000 shares authorized; 40,993,768 and 37,142,946 shares issued and outstanding at December 31, 2021 and December 31, 2020, respectively | 4,090 | 3,697 | ||||
| Additional paid-in capital | 497,342,207 | 417,337,742 | ||||
| Accumulated deficit | (293,171,423) | (186,420,599) | ||||
| Accumulated other comprehensive loss, net | (5,040,163) | (5,044,517) | ||||
| Total stockholders' equity | 199,134,711 | 225,876,323 | ||||
| Total liabilities and stockholders' equity | $ | 218,864,844 | $ | 245,115,213 |
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
| Three Months Ended December 31, | Year Ended December 31, | |||||||||||
| 2021 | 2020 | 2021 | 2020 | |||||||||
| Revenues | $ | 3,277,658 | $ | 2,312,706 | $ | 4,410,356 | $ | 8,185,027 | ||||
| Operating expenses: | ||||||||||||
| Research and development | 20,185,064 | 8,950,572 | 74,541,115 | 49,774,328 | ||||||||
| General and administrative | 3,777,281 | 4,111,929 | 15,413,282 | 13,209,440 | ||||||||
| Impairment loss on construction-in-progress | 3,300,000 | - | 11,370,000 | - | ||||||||
| Total operating expenses | 27,262,345 | 13,062,501 | 101,324,397 | 62,983,768 | ||||||||
| Loss from operations | (23,984,687) | (10,749,795) | (96,914,041) | (54,798,741) | ||||||||
| Other income (expense): | ||||||||||||
| Interest expense | 61,107 | (1,953) | (5,656) | (9,421) | ||||||||
| Interest income | 114,894 | 44,360 | 202,741 | 322,514 | ||||||||
| Other (expense) income, net | (80,635) | (24,735) | (373,868) | 24,147 | ||||||||
| Total other (expense) income, net | 95,366 | 17,672 | (176,783) | 337,240 | ||||||||
| Net loss before income tax benefit | (23,889,321) | (10,732,123) | (97,090,824) | (54,461,501) | ||||||||
| Income tax benefit | - | 110,346 | - | 5,417,024 | ||||||||
| Net loss | $ | (23,889,321) | $ | (10,621,777) | $ | (97,090,824) | $ | (49,044,477) | ||||
| Other comprehensive income (loss) - unrealized gain (loss) on short-term investments | - | (2,245) | 4,354 | (24,361) | ||||||||
| Comprehensive loss | $ | (23,889,321) | $ | (10,624,022) | $ | (97,086,470) | $ | (48,017,632) | ||||
| Net loss per share, basic and diluted | $ | (0.57) | $ | (0.29) | $ | (2.35) | $ | (1.91) | ||||
| Weighted-average common shares outstanding, basic and diluted | 41,705,563 | 36,295,023 | 41,283,498 | 25,637,023 |