Full Press Release Details
WAYNE, Pa., Nov. 06, 2025 (GLOBE NEWSWIRE) -- Avalo Therapeutics, Inc. (Nasdaq: AVTX), a clinical stage biotechnology company fully dedicated to developing IL-1β-based treatments for immune-mediated inflammatory diseases, today announced business updates and financial results for the third quarter of 2025.
“Now that enrollment is complete, we’re fully focused on completing the LOTUS trial, preparing for the data readout in mid-2026, and progressing our Phase 3 planning,” said Dr. Garry Neil, Chief Executive Officer. “This marks an important transition for Avalo as we turn our focus from enrollment to completion of the trial, guided by strong conviction in AVTX-009’s high-affinity inhibition of IL-1β and its potential to deliver meaningful benefit for people living with hidradenitis suppurativa.”
Recent Corporate Highlights and Upcoming Anticipated Milestones:
Third Quarter 2025 Financial Update:
Consolidated Balance Sheets(In thousands, except share and per share data)
| September 30, 2025 | December 31, 2024 | |||||||
| (unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 26,963 | $ | 134,546 | ||||
| Short-term investments | 84,654 | — | ||||||
| Prepaid expenses and other current assets | 2,139 | 4,325 | ||||||
| Restricted cash, current portion | 90 | 19 | ||||||
| Total current assets | 113,846 | 138,890 | ||||||
| Property and equipment, net | 542 | 1,209 | ||||||
| Goodwill | 10,502 | 10,502 | ||||||
| Restricted cash, net of current portion | 210 | 131 | ||||||
| Total assets | $ | 125,100 | $ | 150,732 | ||||
| Liabilities, mezzanine equity and stockholders’ equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 474 | $ | 283 | ||||
| Accrued expenses and other current liabilities | 7,498 | 6,317 | ||||||
| Derivative liability, current | — | 360 | ||||||
| Total current liabilities | 7,972 | 6,960 | ||||||
| Royalty obligation | 2,000 | 2,000 | ||||||
| Deferred tax liability, net | 304 | 270 | ||||||
| Derivative liability, non-current | 23,160 | 8,120 | ||||||
| Other long-term liabilities | 117 | 350 | ||||||
| Total liabilities | 33,553 | 17,700 | ||||||
| Mezzanine equity: | ||||||||
| Series D Preferred Stock—$0.001 par value; 1 share of Series D Preferred Stock authorized at September 30, 2025 and December 31, 2024; 1 share of Series D Preferred Stock issued and outstanding at September 30, 2025 and December 31, 2024 | — | — | ||||||
| Series E Preferred Stock—$0.001 par value; 1 share of Series E Preferred Stock authorized at September 30, 2025 and December 31, 2024; 1 share of Series E Preferred Stock issued and outstanding at September 30, 2025 and December 31, 2024 | — | — | ||||||
| Stockholders’ equity: | ||||||||
| Common stock—$0.001 par value; 200,000,000 shares authorized at September 30, 2025 and December 31, 2024; 17,827,635 and 10,471,934 shares issued and outstanding at September 30, 2025 and December 31, 2024, respectively | 18 | 10 | ||||||
| Series C Preferred Stock—$0.001 par value; 34,326 shares of Series C Preferred Stock authorized at September 30, 2025 and December 31, 2024; 19,364 and 24,896 shares of Series C Preferred Stock issued and outstanding at September 30, 2025 and December 31, 2024, respectively | — | — | ||||||
| Additional paid-in capital | 526,290 | 503,285 | ||||||
| Accumulated other comprehensive income | 41 | — | ||||||
| Accumulated deficit | (434,802 | ) | (370,263 | ) | ||||
| Total stockholders’ equity | 91,547 | 133,032 | ||||||
| Total liabilities, mezzanine equity and stockholders’ equity | $ | 125,100 | $ | 150,732 | ||||
The consolidated balance sheets as of September 30, 2025 and December 31, 2024 have been derived from the reviewed and audited financial statements, respectively, but do not include all of the information and footnotes required by accounting principles generally accepted in the United States for complete financial statements.Consolidated Statements of Operations
(In thousands, except per share data)
| Three Months Ended | Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Revenues: | ||||||||||||||||
| Product revenue, net | $ | — | $ | 249 | $ | — | $ | 249 | ||||||||
| Total revenues, net | — | 249 | — | 249 | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Cost of product sales | $ | — | $ | (714 | ) | $ | — | $ | (453 | ) | ||||||
| Research and development | 13,621 | 9,538 | 36,817 | 16,254 | ||||||||||||
| General and administrative | 5,577 | 4,286 | 16,366 | 12,008 | ||||||||||||
| Acquired in-process research and development | — | — | — | 27,641 | ||||||||||||
| Total operating expenses | 19,198 | 13,110 | 53,183 | 55,450 | ||||||||||||
| Loss from operations | (19,198 | ) | (12,861 | ) | (53,183 | ) | (55,201 | ) | ||||||||
| Other (expense) income: | ||||||||||||||||
| Change in fair value of derivative liability | (12,530 | ) | (1,100 | ) | (14,680 | ) | (6,260 | ) | ||||||||
| Interest income, net | 1,117 | 964 | 3,367 | 2,101 | ||||||||||||
| Excess of initial warrant fair value over private placement proceeds | — | — | — | (79,276 | ) | |||||||||||
| Change in fair value of warrant liability | — | 36,025 | — | 148,071 | ||||||||||||
| Private placement transaction costs | — | — | — | (9,220 | ) | |||||||||||
| Other expense, net | (3 | ) | (5 | ) | (8 | ) | (5 | ) | ||||||||
| Total other (expense) income, net | (11,416 | ) | 35,884 | (11,321 | ) | 55,411 | ||||||||||
| (Loss) income before taxes | (30,614 | ) | 23,023 | (64,504 | ) | 210 | ||||||||||
| Income tax expense (benefit) | 11 | (14 | ) | 35 | — | |||||||||||
| Net (loss) income | $ | (30,625 | ) | $ | 23,037 | $ | (64,539 | ) | $ | 210 | ||||||
| Net (loss) income per share of common stock - basic | $ | (2.19 | ) | $ | 0.98 | $ | (5.47 | ) | $ | 0.01 | ||||||
| Net loss per share of common stock - diluted | $ | (2.19 | ) | $ | (2.83 | ) | $ | (5.47 | ) | $ | (22.63 | ) | ||||
| Weighted average common shares outstanding - basic | 14,000,451 | 5,546,257 | 11,795,810 | 2,491,114 | ||||||||||||
| Weighted average common shares outstanding - diluted | 14,000,451 | 10,784,037 | 11,795,810 | 6,540,963 | ||||||||||||
The unaudited consolidated statements of operations for the three and nine months ended September 30, 2025 and 2024 have been derived from the reviewed financial statements, but do not include all of the information and footnotes required by accounting principles generally accepted in the United States for complete financial statements.
About Avalo Therapeutics
Avalo Therapeutics is a clinical stage biotechnology company fully dedicated to developing IL-1β-based treatments for immune-mediated inflammatory diseases. Our lead asset, AVTX-009, is in a Phase 2 clinical trial for hidradenitis suppurativa (HS). We’re also exploring additional opportunities to make an impact in prevalent indications that have significant remaining unmet needs. For more information about Avalo, please visitwww.avalotx.com.
About AVTX-009
AVTX-009 is a humanized monoclonal antibody (IgG4) that binds to interleukin-1β (IL-1β) with high affinity and neutralizes its activity. IL-1β is a pro-inflammatory cytokine that plays a central role in the pathogenesis of a wide range of human diseases.1It activates immune cells that generate proinflammatory cytokines, including IL-6, TNF-α, and IL-17. Dysregulated IL-1β signaling is a major driver of inflammation, contributing to the progression of autoimmune disorders. IL-1β inhibition has proven effective in multiple immune-mediated inflammatory diseases.1-3
About the LOTUS Trial
The LOTUS trial is a randomized, double-blind, placebo-controlled, parallel-group Phase 2 trial with two AVTX-009 dose regimens to evaluate the efficacy, safety and tolerability of AVTX-009 in approximately 250 adults with moderate to severe hidradenitis suppurativa. Subjects were randomized (1:1:1) to receive either one of two dosing regimens of AVTX-009 or placebo during a 16-week treatment phase. The primary efficacy endpoint is the proportion of subjects achieving Hidradenitis Suppurativa Clinical Response (HiSCR75) at Week 16. Secondary objectives include but are not limited to: the proportion of patients achieving HiSCR50 and HiSCR90 as well as change from baseline in: International HS Severity Score System (IHS4), draining fistula count, abscess and inflammatory nodule (AN) count, and patients achieving at least a 30% reduction on a numerical rating scale in Patient's Global Assessment of Skin Pain (PGA Skin Pain). For additional information this trial (NCT06603077), please visitwww.clinicaltrials.govorwww.lotustrial.com.
About Hidradenitis Suppurativa
Hidradenitis suppurativa (HS) is a chronic, progressive, often debilitating inflammatory skin disease that causes painful nodules, abscesses, and tunnels to form under the skin.4-6,8Areas commonly affected by HS include the nape of the neck, breasts, chest, armpits, abdomen, buttocks and anus, groin and genitals, and inner thighs.7If not adequately and promptly treated, the chronic inflammation characteristic of HS may progress to tissue destruction and permanent scarring.4-6,9HS typically first presents in late adolescence or early adulthood and is estimated to affect 0.7–1.2% of the U.S. population, though some sources suggest the prevalence may be as high as 2–4%.10,11,12
References:1Dinarello CA. Immunol Rev. 2018;281(1):8-27.2Kany S et al. Int J Mol Sci. 2019;20(23):6008.3Kimball AB et al. Presented at: American Academy of Dermatology; March 8-12, 2024; San Diego, CA.4Diaz MJ, et al. Curr Iss Mol Bio. 2023;45:4400-4415.5Agnese ER, et al. Cureus. 2023;15(11):e49390.6de Oliveira ASLE, et al. Biomolecules. 2022;12(10):1371.7Ingram JR, et al. J Eur Acad Dermatol Venereol. 2022;36(9):1597-160.8Sabat R, et al. The Lancet. 2025;405(10476):P420-438.9Jemec GB.Clinicalpractice. Hidradenitis suppurativa.N Engl J Med. 2012;366(2):158–164.10Garg A, Kirby JS, Lavian J, Lin G, Strunk A. Sex- and Age-Adjusted Population Analysis of Prevalence Estimates for Hidradenitis Suppurativa in the United States.JAMA Dermatol. 2017;153(8):760–764. doi:10.1001/jamadermatol.2017.0201.11Ingram, John R.British Journal of Dermatology. doi:10.1111/bjd.19435.12Nguyen TV, et al. J Eur Acad Dermatol Venereol. 2021;35(1):50-61.
Forward-Looking Statements
This press release may include forward-looking statements made pursuant to the Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that are not historical facts. Such forward-looking statements are subject to significant risks and uncertainties that are subject to change based on various factors (many of which are beyond Avalo’s control), which could cause actual results to differ from the forward-looking statements. Such statements may include, without limitation, statements with respect to Avalo’s plans, objectives, projections, expectations and intentions and other statements identified by words such as “projects,” “may,” “might,” “will,” “could,” “would,” “should,” “continue,” “seeks,” “aims,” “predicts,” “believes,” “expects,” “anticipates,” “estimates,” “intends,” “plans,” “potential,” or similar expressions (including their use in the negative), or by discussions of future matters such as: drug development costs, timing of trials and trial results and other risks, including reliance on investigators and enrollment of patients in clinical trials; reliance on key personnel; regulatory risks; general economic and market risks and uncertainties, including those caused by the war in Ukraine and the Middle East; and those other risks detailed in Avalo’s filings with the Securities and Exchange Commission, available atwww.sec.gov. Actual results may differ from those set forth in the forward-looking statements. Except as required by applicable law, Avalo expressly disclaims any obligations or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Avalo’s expectations with respect thereto or any change in events, conditions or circumstances on which any statement is based.