Avalo Reports Third Quarter 2023 Financial Results and Provides Business Updates
- Successful elimination of $35 million debt strengthens the balance sheet and positions the company for future growth and innovation
- Divestiture of AVTX-800 series for potential milestone payments of $45 million provides additional financial resources for research and development
- Improved cash of approximately $10.2 million as of September 30, 2023, reflects positive financial management and liquidity
- None.
- Successfully eliminated
$35 million debt paving the way for future growth and innovation - Divested AVTX-800 series for potential milestone payments of
$45 million , fully focusing the pipeline on Avalo’s promising immunology assets - Disclosed improved cash of approximately
$10.2 million as of September 30, 2023
WAYNE, Pa. and ROCKVILLE, Md., Nov. 09, 2023 (GLOBE NEWSWIRE) -- Avalo Therapeutics, Inc. (Nasdaq: AVTX), today announced business updates and financial results for the third quarter of 2023.
Dr. Garry Neil, Chief Executive Officer and Chairman of the Board remarked, “We made significant progress in the third quarter, highlighted by the full debt payoff and divestiture of the 800 series. Our strengthened balance sheet and focused pipeline underscores our unwavering commitment to execute our strategy to progress our promising immunology drug candidates and positions us to consider collaborations, pursue funding for research and development, and bring innovative treatments to market.”
Dr. Neil continued, “I am excited to potentially kick off a randomized placebo-controlled trial of quisovalimab, our anti-LIGHT mAb, in patients with ulcerative colitis or another inflammatory indication, subject to funding. This drug candidate has previously shown strong target engagement in both acute and chronic inflammatory diseases, and I remain optimistic that it could transform the lives of patients with immunological diseases and address unmet medical needs. Additionally, we look forward to progressing AVTX-008, our BTLA agonist fusion protein with high-binding affinity and serum stability, to IND. Targeting BTLA represents a promising and increasingly recognized avenue for developing therapies that can effectively modulate the immune response in autoimmune diseases while minimizing the risk of systemic immunosuppression. We believe AVTX-008 is unique in this class because it is a fusion protein that utilizes the natural ligand thus avoiding potential problems with agonist mAbs. Finally, we continue to evaluate new opportunities to further augment our immunology pipeline.”
Corporate Updates:
- In September of 2023, Avalo paid off the remaining
$14.3 million of its original$35 million debt owed to Horizon Technology Finance Corporation (Nasdaq: HRZN). As a result, Avalo’s obligations under the debt agreement were deemed satisfied. - On October 27, 2023, Avalo completed the divestiture of its rights, title and interest in, assets relating to AVTX-801, AVTX-802 and AVTX-803 (collectively, the 800 Series) to AUG Therapeutics, LLC (AUG). The Company is entitled to up to
$45 million of contingent milestone payments. The Company previously announced it entered into a purchase agreement with AUG to divest the 800 Series on September 12, 2023.
Program Updates:
- Quisovalimab (AVTX-002): Anti-LIGHT monoclonal antibody (mAb) targeting immune-inflammatory diseases.
- Quisovalimab has shown a rapid and sustained reduction of LIGHT levels, as well as a favorable safety and tolerability profile, in all indications studied including COVID-19 Acute Respiratory Distress Syndrome (ARDS), Crohn’s Disease and Non-Eosinophilic Asthma (NEA).
- Quisovalimab was statistically significant in reducing respiratory failure and mortality in patients hospitalized with COVID-19 ARDS in a randomized placebo-controlled trial. Quisovalimab also demonstrated positive trends in an open-label study in Crohn’s Disease.
- A post-hoc analyses in the PEAK Trial showed a sub-population of NEA patients with baseline LIGHT levels over 125 pg/mL, which represented over
50% of patients, had an approximate50% reduction in asthma-related events (AREs) for patients treated with quisovalimab compared to placebo. - Avalo is pursuing funding for the program and is considering a randomized placebo-controlled trial in patients with Ulcerative Colitis or other inflammatory conditions.
- AVTX-008: B and T Lymphocyte Attenuator (BTLA) agonist fusion protein targeting immune dysregulation disorders.
- AVTX-008 is uniquely positioned as a fusion protein with high-binding affinity and serum stability. It utilizes the natural ligand thus it may avoid the potential problems with agonist mAbs.
- Avalo previously identified a lead molecule, is evaluating several immune dysregulation disorders to pursue and plans to rapidly progress the asset to IND, subject to funding.
Third Quarter 2023 Financial Update:
Avalo had
Total operating expenses decreased
The net loss and net loss per share for the nine months ended September 30, 2023 was largely driven by operating expenses. The significant decrease in net loss for the nine months ended September 30, 2023 as compared to the prior year period was due to the
Consolidated Balance Sheets
(In thousands, except share and per share data)
| September 30, 2023 | December 31, 2022 | |||||||
| (unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 10,180 | $ | 13,172 | ||||
| Other receivables | 1,538 | 1,919 | ||||||
| Inventory, net | — | 20 | ||||||
| Prepaid expenses and other current assets | 940 | 1,290 | ||||||
| Restricted cash, current portion | 1 | 15 | ||||||
| Total current assets | 12,659 | 16,416 | ||||||
| Property and equipment, net | 2,071 | 2,411 | ||||||
| Goodwill | 14,409 | 14,409 | ||||||
| Restricted cash, net of current portion | 131 | 131 | ||||||
| Total assets | $ | 29,270 | $ | 33,367 | ||||
| Liabilities and stockholders’ equity (deficit) | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 789 | $ | 2,882 | ||||
| Deferred revenue | — | 88 | ||||||
| Accrued expenses and other current liabilities | 5,216 | 13,214 | ||||||
| Notes payable, current | — | 5,930 | ||||||
| Total current liabilities | 6,005 | 22,114 | ||||||
| Notes payable, non-current | — | 13,486 | ||||||
| Royalty obligation | 2,000 | 2,000 | ||||||
| Deferred tax liability, net | 164 | 141 | ||||||
| Derivative liability | 4,950 | 4,830 | ||||||
| Other long-term liabilities | 1,456 | 1,711 | ||||||
| Total liabilities | 14,575 | 44,282 | ||||||
| Stockholders’ equity (deficit): | ||||||||
| Common stock— | 192 | 9 | ||||||
| Additional paid-in capital | 341,469 | 292,900 | ||||||
| Accumulated deficit | (326,966 | ) | (303,824 | ) | ||||
| Total stockholders’ equity (deficit) | 14,695 | (10,915 | ) | |||||
| Total liabilities and stockholders’ equity (deficit) | $ | 29,270 | $ | 33,367 | ||||
The condensed consolidated balance sheets as of September 30, 2023 and December 31, 2022 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 accepted in the United States for complete financial statements.
Consolidated Statements of Operations (Unaudited)
(In thousands, except per share data)
| Three Months Ended | Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||||||
| Revenues: | ||||||||||||||||
| Product revenue, net | $ | 236 | $ | 432 | $ | 1,353 | $ | 2,638 | ||||||||
| License revenue | — | 14,517 | — | 14,517 | ||||||||||||
| Total revenues, net | 236 | 14,949 | 1,353 | 17,155 | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Cost of product sales | 247 | 528 | 1,505 | 2,814 | ||||||||||||
| Research and development | 1,249 | 7,042 | 11,917 | 25,136 | ||||||||||||
| Selling, general and administrative | 2,490 | 3,284 | 7,624 | 17,752 | ||||||||||||
| Amortization expense | — | — | — | 38 | ||||||||||||
| Total operating expenses | 3,986 | 10,854 | 21,046 | 45,740 | ||||||||||||
| (3,750 | ) | 4,095 | (19,693 | ) | (28,585 | ) | ||||||||||
| Other expense: | ||||||||||||||||
| Interest expense, net | (1,553 | ) | (898 | ) | (3,498 | ) | (3,221 | ) | ||||||||
| Change in fair value of derivative liability | 100 | — | (120 | ) | — | |||||||||||
| Other expense, net | (17 | ) | — | (42 | ) | (20 | ) | |||||||||
| Total other expense, net | (1,470 | ) | (898 | ) | (3,660 | ) | (3,241 | ) | ||||||||
| (Loss) income before taxes | (5,220 | ) | 3,197 | (23,353 | ) | (31,826 | ) | |||||||||
| Income tax expense | 8 | 5 | 23 | 20 | ||||||||||||
| Net (loss) income and comprehensive loss | $ | (5,228 | ) | $ | 3,192 | $ | (23,376 | ) | $ | (31,846 | ) | |||||
| Net (loss) income per share of common stock, basic and diluted | $ | (0.11 | ) | $ | 0.34 | $ | (0.96 | ) | $ | (3.39 | ) | |||||
The unaudited condensed consolidated statements of operations for the three and nine months ended September 30, 2023 and 2022 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 quisovalimab (AVTX-002)
Quisovalimab is a fully human monoclonal antibody (mAb), directed against human LIGHT (Lymphotoxin-like, exhibits Inducible expression, and competes with Herpes Virus Glycoprotein D for Herpesvirus Entry Mediator (HVEM), a receptor expressed by T lymphocytes). There is increasing evidence that the dysregulation of the LIGHT-signaling network which includes LIGHT, its receptors HVEM and LTβR and the downstream checkpoint BTLA, is a disease-driving mechanism in autoimmune and inflammatory reactions in barrier organs. Therefore, we believe reducing LIGHT levels can moderate immune dysregulation in many acute and chronic inflammatory disorders. Quisovalimab previously demonstrated proof of concept in COVID-19 induced acute respiratory distress syndrome including reduction in mortality and respiratory failure, as well as a positive signal in patients with Crohn’s Disease.
About AVTX-008
AVTX-008 is a fully human B and T Lymphocyte Attenuator (BTLA) agonist fusion protein in the IND-enabling stage. AVTX-008 is differentiated by having specific binding to BTLA, with no binding to LIGHT or CD160. AVTX-008 also has high-serum stability and solubility.
About Avalo Therapeutics
Avalo Therapeutics is a clinical stage biotechnology company focused on the treatment of immune dysregulation by developing therapies that target the LIGHT-signaling network.
LIGHT and its signaling receptors, HVEM (TNFRSF14), and lymphotoxin β receptor (TNFRSF3), form an immune regulatory network with two co-receptors of herpesvirus entry mediator, checkpoint inhibitor B and T Lymphocyte Attenuator (BTLA), and CD160 (the LIGHT-signaling network). Accumulating evidence points to the dysregulation of the LIGHT network as a disease-driving mechanism in autoimmune and inflammatory reactions in barrier organs. Therefore, we believe reducing LIGHT levels can moderate immune dysregulation in many acute and chronic inflammatory disorders.
For more information about Avalo, please visit www.avalotx.com.
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: the future financial and operational outlook; timing and success of trial results and regulatory review; potential attributes and benefits of product candidates; the development of product candidates or products; and other statements that are not historical. These statements are based upon the current beliefs and expectations of Avalo’s management but are subject to significant risks and uncertainties, including: Avalo's cash position and the need for it to raise additional capital in the near future; the results of our clinical and pre-clinical studies; drug development costs, timing and other risks, including reliance on investigators and enrollment of patients in clinical trials, which might be slowed by the COVID-19 pandemic; reliance on key personnel; regulatory risks; general economic and market risks and uncertainties, including those caused by the COVID-19 pandemic and the war in Ukraine; and those other risks detailed in Avalo’s filings with the SEC. 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.
For media and investor inquiries
Christopher Sullivan, CFO
Avalo Therapeutics, Inc.
ir@avalotx.com
410-803-6793
or
Chris Brinzey
ICR Westwicke
Chris.brinzey@westwicke.com
339-970-2843
FAQ
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