AAvalo Therapeutics develops biologic therapies that target the IL-1beta pathway for immune-mediated inflammatory diseases. Its lead candidate, abdakibart (AVTX-009), is a humanized monoclonal antibody that inhibits IL-1beta and blocks downstream inflammatory signaling, advancing toward a registrational Phase 3 program after positive Phase 2 results in hidradenitis suppurativa. AVTX-010 is a long-acting next-generation anti-IL-1beta antibody designed to extend dosing intervals. The company focuses on research and development of novel biologics with commercialization expected through pharmaceutical partnerships and product sales. Unlike some competitors that pursue broader or different inflammatory targets, Avalo concentrates specifically on IL-1beta–related inflammation with a pipeline aimed at improving dosing convenience and clinical outcomes in inflammatory diseases.
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Industries
Company Size
51-200
Company Stage
IPO
Headquarters
Rockville, MD
Founded
2011
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Total Funding
$1.2B
Above
Industry Average
Funded Over
12 Rounds
Avalo Therapeutics has secured $472 million in funding to advance its drug development programmes through 2029. The biotech company is focused on abdakibart, its lead treatment for hidradenitis suppurativa, which demonstrated strong efficacy and safety in Phase II trials across both biologic-experienced and treatment-naive patients. The funding will support registrational-stage development, including upcoming Phase 3 trials for abdakibart. Avalo is also developing AVTX-010, designed to improve dosing intervals and extend intellectual property protection. The financing reduces near-term dilution risk and strengthens the company's position as it pursues opportunities in the hidradenitis suppurativa treatment market.
Avalo Therapeutics reported second quarter 2026 financial results, with cash, cash equivalents and investments of $472.2 million as of 30 June 2026, expected to fund operations into 2029. The clinical stage biotechnology company plans to initiate a registrational Phase 3 programme evaluating abdakibart in hidradenitis suppurativa in the first half of 2027. The company also expanded its pipeline with AVTX-010, a long-acting anti-IL-1β antibody, with an Investigational New Drug application planned for the first half of 2027. Research and development expenses were $23.4 million for the second quarter, up $9.3 million from the same period in 2025. Net loss was $36.4 million, an increase of $15.6 million year-on-year. Net cash used in operating activities was $37.7 million for the six months ended 30 June 2026.
Avalo Therapeutics appoints Ron Philip to Board of Directors. WAYNE, Pa., June 23, 2026 (GLOBE NEWSWIRE) - Avalo Therapeutics, Inc. (Nasdaq: AVTX), a clinical-stage biotechnology company fully dedicated to developing therapeutics targeting the IL-1β pathway for immune-mediated inflammatory diseases, today announced the appointment of Ron Philip to its Board of Directors. Mr. Philip brings more than 30 years of biopharmaceutical leadership to the Board, with a deep background in commercial and strategic execution, including guiding multiple companies through product launches and billion dollar exits. "We are thrilled to welcome Ron to the Board at this pivotal time for Avalo following our positive Phase 2 LOTUS topline results and transformative financing," said Garry Neil, MD, Chief Executive Officer of Avalo Therapeutics. "Ron's strategic and commercial expertise, including his proven success bringing novel therapies to market, will be invaluable as we advance abdakibart in hidradenitis suppurativa (HS) into phase 3 and beyond. We look forward to his guidance as we work to deliver this important therapy to patients." "I am excited to join Avalo's Board following the compelling Phase 2 topline data for abdakibart in HS, which highlight its potential to become a best-in-disease treatment," said Ron Philip. "The trial demonstrated potential leading efficacy, a favorable safety profile, and the convenience of monthly dosing, attributes that are the cornerstones of a successful commercial product. I look forward to sharing my experience to help shape the strategic and commercial plan and ultimately bring this differentiated new treatment option to the HS community." Mr. Philip currently serves as Executive Chair of CREATE Medicines. Previously, he served as Chief Executive Officer of Orbital Therapeutics, where he led the company through its $1.5 billion acquisition by Bristol Myers Squibb. Prior to Orbital, Mr. Philip held a series of senior leadership positions at Spark Therapeutics, ultimately serving as Chief Executive Officer. Earlier, he served as Chief Operating Officer and Chief Commercial Officer, leading the commercial launch of LUXTURNA(R), Spark's first FDA-approved gene therapy and the first gene therapy approved in the United States for a genetic disease. During his tenure, he also played a key leadership role in Spark's $4.8 billion acquisition by Roche. Earlier in his career, Mr. Philip held senior strategy, commercial, and operational leadership roles at Pfizer and Wyeth, where he supported several successful medicines, including ENBREL(R) and XELJANZ(R). He currently serves on the boards of Harmony Biosciences and City Therapeutics. Mr. Philip is a graduate of Drexel University. About Avalo Therapeutics Avalo Therapeutics is a clinical stage biotechnology company fully dedicated to developing therapeutics targeting the IL-1β pathway for immune-mediated inflammatory diseases. Its lead asset, abdakibart, is an anti-IL-1β monoclonal antibody (mAb). Positive topline data was recently reported for abdakibart in a Phase 2 clinical trial in hidradenitis suppurativa (HS). In addition to HS, Avalotx is exploring additional opportunities to make an impact in prevalent indications that have significant remaining unmet needs. Avalotx is also advancing AVTX-010, a long-acting next-generation anti-IL-1β mAb designed to extend dosing intervals and build upon the differentiated profile established by abdakibart. For more information about Avalo, please visit www.avalotx.com. About Abdakibart Abdakibart 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.1 It 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] References:[1] Dinarello CA. Immunol Rev. 2018;281(1):8-27. [2] Kany S et al. Int J Mol Sci. 2019;20(23):6008. [3] Kimball AB et al. Presented at: American Academy of Dermatology; March 8-12, 2024; San Diego, CA. Forward-Looking Statements This press release includes forward-looking statements made pursuant to the Private Securities Litigation Reform Act of 1995 and other federal securities laws. 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 its control), which could cause actual results to differ from the forward-looking statements. Such statements may include, without limitation, statements with respect to its 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: therapeutic potential, clinical benefits and safety profiles of abdakibart (AVTX-009); plans to advance abdakibart into a registrational phase 3 program; plans to commercialize abdakibart; expectations regarding timing, success and data announcements of ongoing preclinical studies and clinical trials; drug development costs, reliance on investigators and enrollment of patients in clinical trials; and its plans to develop and commercialize its current and any future product candidates and the implementation of its business model and strategic plans for its business. Any forward-looking statements are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements including, without limitation, risks associated with: the timing and anticipated results of its current and future preclinical studies and clinical trials, supply chain, strategy and future operations; the delay of any current and future preclinical studies or clinical trials or the development of its product candidates; the risk that the results of prior preclinical studies and clinical trials may not be predictive of future results in connection with current or future preclinical studies and clinical trials, including those for abdakibart; the timing and outcome of any interactions with regulatory authorities; obtaining, maintaining and protecting its intellectual property; the availability of funding sufficient for its operating expenses and capital expenditure requirements, 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 its filings with the Securities and Exchange Commission, available at www.sec.gov. Avalotx may not actually achieve the plans, intentions or expectations disclosed in its forward-looking statements, and you should not place undue reliance on its forward-looking statements. In addition, any forward-looking statements represent its view only as of today and should not be relied upon as representing its views as of any subsequent date. You should not rely upon forward-looking statements as predictions of future events and actual results or events could differ materially from the plans, intentions and expectations disclosed herein. Except as required by applicable law, Avalotx expressly disclaim any obligations or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in its 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. [email protected] 410-803-6793 Meru Advisors Lauren Glaser [email protected] Released June 23, 2026
WAYNE, Pa., May 05, 2026 (GLOBE NEWSWIRE) -- Avalo Therapeutics, Inc. (NASDAQ: AVTX) (“Avalo”), a clinical-stage biotechnology company…...
Avalo Therapeutics has priced a public offering at $17.75 per share, selling 19,730,000 shares of common stock and 1,400,000 pre-funded warrants, with expected gross proceeds of approximately $375 million. The funds will advance clinical development of abdakibart, particularly for Phase 3 topline data release, as well as working capital and general corporate purposes. Leerink Partners, TD Cowen, BofA Securities, Piper Sandler and Cantor are acting as joint bookrunning managers for the offering. The offering is being conducted under an S-3 registration statement filed with the SEC on 8 January 2026.
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Industries
Company Size
51-200
Company Stage
IPO
Headquarters
Rockville, MD
Founded
2011
Find jobs on Simplify and start your career today
Don't see your dream role? Check out thousands of other roles on Simplify.Browse all jobs