Full Press Release Details
Altimmune Announces First Quarter 2024 Financial Results and Provides a Business Update
Enrollment ongoing in IMPACT Phase 2b trial of pemvidutide in Metabolic Dysfunction-Associated Steatohepatitis (MASH), with top line results expected in Q1 2025
Cash, cash equivalents and short-term investments of $182.1 million at March 31, 2024
Webcast to be held today, May 9, 2024, at 8:30 am ET
GAITHERSBURG, MD - May 9, 2024 - Altimmune, Inc. (Nasdaq: ALT), a clinical-stage biopharmaceutical company, today announced financial results for the first quarter ended March 31, 2024, and provided a business update.
"As the obesity therapeutics space evolves, increasing attention is being placed on agents that are able to drive weight loss while addressing the quality of that weight loss and the comorbidities of obesity. With significant weight loss, preservation of lean mass and reductions in serum lipids and liver fat achieved in our clinical trials, we believe that pemvidutide could differentiate itself from other therapies in this competitive market. With these promising data, we are preparing for our End-of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA), which is expected to occur late in the third quarter. This meeting is expected to provide further clarity regarding the Phase 3 pemvidutide obesity registrational program, and we look forward to our upcoming interactions with the Agency," said Vipin K. Garg, Ph.D., President and Chief Executive Officer of Altimmune. "Further, we continue to advance IMPACT, our Phase 2b trial of pemvidutide in MASH, with top line results expected in the first quarter of 2025."
Recent Highlights and Anticipated Milestones:
Financial Results for the Three Months Ended March 31, 2024
Conference Call Information:
| Date: | Thursday, May 9, 2024 |
| Time: | 8:30 am Eastern Time |
| Webcast: | To listen, the conference call will be webcast live on Altimmune's Investor Relations website at https://ir.altimmune.com/investors . |
| Dial-in: | To participate or dial-in, register here to receive the dial-in numbers and unique PIN to access the call. |
Following the conclusion of the call, the webcast will be available for replay on the Investor Relations (IR) 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 MASH. 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. Glucagon is also recognized as having direct effects on hepatic fat metabolism, leading to rapid reductions in levels of liver fat and serum lipids. In clinical trials, once-weekly pemvidutide has shown compelling weight loss, robust reductions in triglycerides, LDL cholesterol, liver fat content and blood pressure with a clean safety profile to date. The U.S. FDA has granted Fast Track designation to pemvidutide for the treatment of MASH. Pemvidutide has recently completed the MOMENTUM Phase 2 obesity trial and is being studied in the IMPACT Phase 2b MASH trial.
Altimmune is a clinical-stage biopharmaceutical company focused on developing innovative next-generation peptide-based therapeutics. The Company is developing pemvidutide, a GLP-1/glucagon dual receptor agonist for the treatment of obesity and MASH. 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, and the prospects for the utility of, 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. 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: 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 most recent annual report on Form 10-K and our other filings with the SEC, which are available at www.sec.gov.
| Rich Eisenstadt |
| Chief Financial Officer |
| Phone: 240-654-1450 |
| ir@altimmune.com |
| Lee Roth Burns McClellan |
| Phone: 646-382-3403 |
| lroth@burnsmc.com |
| Julia Weilman Burns McClellan |
| Phone: 646-732-4443 |
| jweilman@burnsmc.com |
| Danielle Cantey |
| Inizio Evoke, Biotech |
| Phone: 619-826-4657 |
| Danielle.cantey@inizioevoke.com |
CONSOLIDATED BALANCE SHEETS
(In thousands, except share and per-share amounts)
| March 31, | December 31, | |||||
| 2024 | 2023 | |||||
| (Unaudited) | ||||||
| ASSETS | ||||||
| Current assets: | ||||||
| Cash and cash equivalents | $ | 78,978 | $ | 135,117 | ||
| Restricted cash | 41 | 41 | ||||
| Total cash, cash equivalents and restricted cash | 79,019 | 135,158 | ||||
| Short-term investments | 103,046 | 62,698 | ||||
| Accounts and other receivables | 307 | 1,111 | ||||
| Income tax and R&D incentive receivables | 2,272 | 3,742 | ||||
| Prepaid expenses and other current assets | 2,871 | 6,917 | ||||
| Total current assets | 187,515 | 209,626 | ||||
| Property and equipment, net | 544 | 651 | ||||
| Other assets | 299 | 363 | ||||
| Total assets | $ | 188,358 | $ | 210,640 | ||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||
| Current liabilities: | ||||||
| Accounts payable | $ | 3,760 | $ | 2,070 | ||
| Accrued expenses and other current liabilities | 7,573 | 10,073 | ||||
| Total current liabilities | 11,333 | 12,143 | ||||
| Noncurrent liabilities | 4,088 | 4,398 | ||||
| Total liabilities | 15,421 | 16,541 | ||||
| Commitments and contingencies | ||||||
| Stockholders' equity: | ||||||
| Common stock, $0.0001 par value; 200,000,000 shares authorized; 70,899,134 and 70,677,400 shares issued and outstanding as of March 31, 2024 and December 31, 2023, respectively | 7 | 7 | ||||
| Additional paid-in capital | 668,816 | 665,427 | ||||
| Accumulated deficit | (490,725) | (466,331) | ||||
| Accumulated other comprehensive loss, net | (5,161) | (5,004) | ||||
| Total stockholders' equity | 172,937 | 194,099 | ||||
| Total liabilities and stockholders' equity | $ | 188,358 | $ | 210,640 |
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(In thousands, except share and per-share amounts)
| Three Months Ended | ||||||
| March 31, | ||||||
| 2024 | 2023 | |||||
| Revenues | $ | 5 | $ | 21 | ||
| Operating expenses: | ||||||
| Research and development | 21,487 | 17,249 | ||||
| General and administrative | 5,312 | 4,531 | ||||
| Total operating expenses | 26,799 | 21,780 | ||||
| Loss from operations | (26,794) | (21,759) | ||||
| Other income (expense): | ||||||
| Interest expense | (1) | (2) | ||||
| Interest income | 2,413 | 1,668 | ||||
| Other income (expense), net | (12) | 19 | ||||
| Total other income (expense), net | 2,400 | 1,685 | ||||
| Net loss | (24,394) | (20,074) | ||||
| Other comprehensive income - unrealized (loss) gain on short-term investments | (157) | 126 | ||||
| Comprehensive loss | $ | (24,551) | $ | (19,948) | ||
| Net loss per share, basic and diluted | $ | (0.34) | $ | (0.40) | ||
| Weighted-average common shares outstanding, basic and diluted | 70,801,713 | 50,125,685 |