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Altimmune Announces First Quarter 2025 Financial Results and Business Update

1. Top-line data from IMPACT trial expected in Q2 2025. 2. Phase 2 trials for AUD and ALD starting in Q2 and Q3 2025. 3. $150 million cash and a $100 million credit facility enhance financial strength. 4. Pemvidutide shows potential as best-in-class for MASH with significant weight loss. 5. Net loss decreased to $19.6 million from $24.4 million year-over-year.

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Why Bullish?

Upcoming trial outcomes often result in volatility. Historical trends show positive data leads to price surges.

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The article highlights significant milestones and financial strength, indicating solid future performance.

Why Short Term?

Results expected in Q2 2025 could quickly influence market perception and price.

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May 13, 2025 07:00 ET  | Source: Altimmune, Inc Top-line data from IMPACT Phase 2b trial of pemvidutide in metabolic dysfunction-associated steatohepatitis (MASH) expected in Q2 2025 Phase 2 trials in Alcohol Use Disorder (AUD) and Alcohol Liver Disease (ALD), expected to initiate in Q2 and Q3 2025, respectively Cash, cash equivalents and short-term investments of $150 million as of March 31, 2025 $100 million credit facility secured with Hercules Capital, adding balance sheet strength and financial flexibility to support continued development of pemvidutide Webcast to be held today, May 13, 2025, at 8:30 a.m. ET GAITHERSBURG, Md., May 13, 2025 (GLOBE NEWSWIRE) -- Altimmune, Inc. (Nasdaq: ALT), a late clinical-stage biopharmaceutical company developing novel peptide-based therapeutics for liver and cardiometabolic diseases, today announced financial results for the first quarter ended March 31, 2025, and provided a business update. “The first quarter of 2025 was productive for Altimmune as the Company approaches a number of important milestones,” said Vipin K. Garg, Ph.D., President and Chief Executive Officer of Altimmune. “The readout of our IMPACT Phase 2b trial of pemvidutide in MASH is on-track for the second quarter of 2025. We believe that achieving statistical significance on MASH resolution and fibrosis improvement at only 24 weeks, coupled with clinically meaningful weight loss, would position pemvidutide as the best-in-class therapeutic candidate for the treatment of MASH.” Dr. Garg continued, “At our recent R&D Day event we unveiled two additional indications for pemvidutide in AUD and ALD, and our intent to initiate Phase 2 clinical trials in these indications in Q2 and Q3, respectively. AUD and ALD are conditions of significant unmet medical need with limited treatment options. We remain committed to developing pemvidutide for treatment of liver and cardiometabolic diseases that leverage its differentiated clinical profile.” Recent Highlights and Anticipated Milestones MASH Top-line data from the IMPACT Phase 2b trial of pemvidutide in biopsy-confirmed F2/F3 MASH expected in Q2 2025 Top-line data is expected to include rates of MASH resolution and fibrosis improvement, weight loss, non-invasive tests, and data on safety and tolerability.A total of 212 participants were randomized, exceeding the 190 originally planned.If successful, pemvidutide would be the first investigational therapy in MASH to achieve statistical significance in both MASH resolution and fibrosis improvement, as well as demonstrate meaningful weight loss, after only 24 weeks of treatment. Altimmune presented new data at the EASL International Liver Congress™ 2025, including a follow-on analysis of the Company’s Phase 1b trial in MASLD using the MASH Resolution Index (MASHResInd). Developed by Dr. Rohit Loomba, Professor of Medicine and Chief of Gastroenterology and Hepatology at the University of California San Diego, MASHResInd is a non-invasive measure that has been highly predictive of MASH resolution.The analyses indicated that after 24 weeks of treatment, the proportion of participants receiving pemvidutide achieving MASHResInd responses exceeded 90%. These findings indicate that high rates of MASH resolution may be observed in the upcoming IMPACT Phase 2b MASH trial readout. Additional Indications for Pemvidutide: AUD and ALD During Altimmune’s R&D Day, the Company announced the development of pemvidutide in two additional indications: AUD and ALD AUD and ALD are characterized by large patient populations with significant unmet medical need and very few treatment options.Investigational New Drug (IND) applications were cleared by the FDA in the first quarter of 2025. The Phase 2 trials in AUD and ALD are expected to initiate in the second and third quarters of 2025, respectively.Preclinical data and data from other clinical trials support the potential of pemvidutide to reduce alcohol consumption, improve liver health, and provide the added benefit of meaningful weight loss. Corporate Update The Company entered into a $100 million credit facility with Hercules Capital, with an initial $15 million tranche funded at closing. An additional $25 million is available in 2025 at Altimmune’s option, subject to the achievement of certain clinical and financial milestones. The remaining $60 million is available beginning in 2026, with $15 million subject to the achievement of certain clinical and financial milestones and up to $45 million available subject to approval of Hercules. The credit facility significantly increases Altimmune’s financial strength and flexibility on attractive terms. Financial Results for the Three Months Ended March 31, 2025 Altimmune reported cash, cash equivalents and short-term investments totaling $150 million on March 31, 2025.Research and development expenses were $15.8 million for the three months ended March 31, 2025, compared to $21.5 million in the same period in 2024, the decrease resulting from timing of clinical trial costs. The expenses for the quarter ended March 31, 2025, included $9.2 million in direct costs related to pemvidutide development activities.General and administrative expenses were $6.0 million for the three months ended March 31, 2025, compared to $5.3 million in the same period in 2024. The increase was primarily due to a $0.5 million increase in stock compensation and other labor-related expenses.Interest income was $1.5 million for the three months ended March 31, 2025, compared to $2.4 million for the same period in 2024.Net loss for the three months ended March 31, 2025, was $19.6 million, or $0.26 net loss per share, compared to a net loss of $24.4 million, or $0.34 net loss per share, in the same period in 2024. Conference Call Information: Date:May 13, 2025Time:8:30 a.m. Eastern TimeWebcast: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. About Pemvidutide Pemvidutide is a novel, investigational, peptide-based 1:1 GLP-1/glucagon dual receptor agonist in development for the treatment of MASH, obesity, Alcohol Use Disorder (AUD) and Alcohol Liver Disease (ALD). 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, which is believed to lead to rapid reductions in levels of liver fat and serum lipids. In clinical trials to date, once-weekly pemvidutide has demonstrated compelling weight loss with class-leading lean mass preservation, and robust reductions in triglycerides, LDL cholesterol, liver fat content and blood pressure. The U.S. FDA has granted Fast Track designation to pemvidutide for the treatment of MASH. Pemvidutide completed the MOMENTUM Phase 2 obesity trial in 2024 and is being studied in the ongoing IMPACT Phase 2b MASH trial with top line results expected in late June 2025. IND applications in AUD and ALD have received FDA clearance with Phase 2 trials scheduled to commence in Q2 and Q3 2025, respectively. About Altimmune Altimmune is a late clinical-stage biopharmaceutical company focused on developing novel peptide-based therapeutics for liver and cardiometabolic diseases. The Company’s lead program is pemvidutide, a GLP-1/glucagon dual receptor agonist for the treatment of MASH, obesity, Alcohol Use Disorder (AUD) and Alcohol Liver Disease (ALD). For more information, please visit www.altimmune.com. Follow @Altimmune, Inc. on LinkedInFollow @AltimmuneInc on X Forward-Looking Statement Any statements made in this press release related to the use of our credit facility with Hercules, development or commercialization of product candidates and other business and financial matters, including without limitation, trial results and data, 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. Company Contact:Greg WeaverChief Financial OfficerPhone: 240-654-1450ir@altimmune.com Investor Contact:Lee RothBurns McClellanPhone: 646-382-3403lroth@burnsmc.com Media Contact:Jake RobisonInizio Evoke CommsPhone: 619-849-5383jake.robison@inizioevoke.com   ALTIMMUNE, INC.CONSOLIDATED BALANCE SHEETS(In thousands, except share and per-share amounts)   March 31, December 31,  2025  2024   (Unaudited)   ASSETS      Current assets:      Cash and cash equivalents $49,104  $36,926 Restricted cash  42   42 Total cash, cash equivalents and restricted cash  49,146   36,968 Short-term investments  100,722   94,965 Accounts and other receivables  507   544 Income tax and R&D incentive receivables  1,957   2,573 Prepaid expenses and other current assets  2,930   2,204 Total current assets  155,262   137,254 Property and equipment, net  384   413 Other assets  1,617   1,639 Total assets $157,263  $139,306 LIABILITIES AND STOCKHOLDERS’ EQUITY      Current liabilities:      Accounts payable $1,077  $211 Accrued expenses and other current liabilities  8,721   10,257 Total current liabilities  9,798   10,468 Other noncurrent liabilities  5,303   5,330 Total liabilities  15,101   15,798 Commitments and contingencies      Stockholders’ equity:      Common stock, $0.0001 par value; 200,000,000 shares authorized; 77,825,450 and 72,352,701 shares issued and outstanding as of March 31, 2025 and December 31 2024, respectively  8   7 Additional paid-in capital  728,122   689,864 Accumulated deficit  (580,965)  (561,390)Accumulated other comprehensive loss, net  (5,003)  (4,973)Total stockholders’ equity  142,162   123,508 Total liabilities and stockholders’ equity $157,263  $139,306           ALTIMMUNE, INC.CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS(In thousands, except share and per-share amounts)   Three Months Ended  March 31,  2025  2024 Revenues $5  $5 Operating expenses:      Research and development  15,827   21,487 General and administrative  5,993   5,312 Total operating expenses  21,820   26,799 Loss from operations  (21,815)  (26,794)Other income (expense):      Interest expense  (1)  (1)Interest income  1,545   2,413 Other income (expense), net  15   (12)Total other income (expense), net  1,559   2,400 Net loss before income taxes  (20,256)  (24,394)Income tax expense (benefit)  (681)  — Net loss  (19,575)  (24,394)Other comprehensive income — unrealized gain on short-term investments  (30)  (157)Comprehensive loss $(19,605) $(24,551)Net loss per share, basic and diluted $(0.26) $(0.34)Weighted-average common shares outstanding, basic and diluted  75,547,746   70,801,713          This press release was published by a CLEAR® Verified individual.

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