InflaRx Reports Second Quarter 2026 Results and Highlights Key Achievements and Expected Milestones
Rhea-AI Summary
InflaRx (Nasdaq: IFRX) reported second quarter 2026 results and a strategic refocus on izicopan, its next-generation oral C5aR inhibitor, for ANCA-associated vasculitis (AAV) and select renal diseases including aHUS, IgAN and C3G. Phase 2 planning in AAV and open-label renal proof-of-concept studies are underway, with initial renal data targeted for 2027.
InflaRx plans a PK bridging study with izicopan in China in late 2026 to accelerate additional inflammation and immunology indications and intends to engage EMA on vilobelimab and izicopan in AAV following CHMP’s recommendation to revoke Tavneos’ EU marketing authorization. In May, the company completed a $150 million underwritten offering (75 million shares at $2.00), generating €119.3 million net, strengthening total funds to €158.4 million at June 30, 2026, which management expects will fund operations and development through 2029.
For the six months ended June 30, 2026, InflaRx recorded a net loss of €16.2 million (€0.17 per share), improved from €22.7 million (€0.35 per share) a year earlier, driven by lower R&D, sales and marketing, and G&A expenses.
Positive
- Equity financing €119.3m net proceeds from May 2026 offering
- Liquidity €158.4m total funds at June 30, 2026; runway projected through 2029
- Net loss reduced to €16.2m H1 2026 from €22.7m H1 2025
- Operating cash outflow cut to €10.0m H1 2026 from €21.6m H1 2025
- R&D expenses decreased to €8.9m H1 2026 from €14.2m H1 2025
- G&A expenses decreased to €5.7m H1 2026 from €8.3m H1 2025
Negative
- Continuing losses €16.2m net loss and €0.17 loss per share H1 2026
- No revenues reported for H1 2026 versus minor revenues in H1 2025
- Share dilution 75m new shares issued at $2.00 in May 2026
- Net financial result swung to €2.0m loss H1 2026 from €3.2m gain H1 2025
- Liabilities to warrant holders increased to €13.27m at June 30, 2026 from €5.80m at year-end 2025
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Mar 19 | Full-year earnings | Positive | +3.4% | Positive Phase 2a data and improved cash runway supported the full-year update. |
| Aug 07 | Second-quarter earnings | Negative | -3.0% | Trial futility and a stopped Phase 3 program accompanied quarterly financial results. |
| May 07 | First-quarter earnings | Positive | -7.5% | Regulatory approval and upcoming clinical catalysts accompanied an improved quarterly loss. |
| Mar 20 | Full-year earnings | Positive | -1.6% | European approval and clinical milestones were reported alongside 2024 financial results. |
| Nov 08 | Third-quarter earnings | Negative | +3.3% | Higher year-to-date net loss offset development milestones and planned clinical data. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Tag-specific earnings reactions were mixed, with three negative and two positive responses and an average move of -1.06%.
Key Terms
pharmacokinetic medical
CYP3A4 medical
pre-funded warrants financial
registered direct offering financial
AI-generated analysis. How Rhea-AI works. Not financial advice.
- Announced advancement of izicopan in ANCA-associated vasculitis (AAV) and select renal diseases; clinical preparations ongoing as planned
- Initiated feasibility assessment for broadened strategy for AAV in Europe Reported new pre-clinical data supporting the safety and differentiation of izicopan as a next-generation oral inhibitor of C5aR
- Pharmacokinetic (PK) bridging study in China expected to start late this year, with a goal to accelerate izicopan proof-of-concept studies in additional inflammation and immunology (I&I) indications
- Virtual Capital Markets Day planned for October 8, 2026 in the morning ET
- Cash, cash equivalents and marketable securities totaled
€158.4 million on June 30, 2026, including net proceeds from the underwritten public offering completed in May, expected to fund ongoing operations and clinical development through 2029
Jena, Germany, Aug. 06, 2026 (GLOBE NEWSWIRE) -- InflaRx N.V. (Nasdaq: IFRX), a biopharmaceutical company pioneering anti-inflammatory therapeutics by targeting the complement system, today announced financial results for the three months ended June 30, 2026, and provided a business update.
Prof. Niels C. Riedemann, Chief Executive Officer and Founder of InflaRx, said: “The second quarter was one of major momentum for InflaRx, as we focused on addressing the growing unmet need in ANCA-associated vasculitis, a rare but devastating inflammatory disease. As we track the evolving regulatory environment in AAV, we believe InflaRx is well positioned to bring the important C5a/C5aR inhibition mechanism forward to help patients. We are making substantial progress with Phase 2 planning for izicopan in AAV, while monitoring dynamic regulatory environments in the U.S. and overseas. Our focus remains on bringing novel and much-needed treatment options to patients in AAV and beyond, and we look forward to reporting additional progress in the coming months.”
Select Recent Highlights and Business Update
Progress with izicopan, next-generation oral C5aR inhibitor,
and plans for further development
In May 2026, InflaRx announced it intends to develop izicopan in AAV, a rare, life-threatening autoimmune disease characterized by inflammation and damage to small blood vessels, with patients often experiencing renal impairment. Phase 2 planning for izicopan in AAV continues as planned.
The Company also announced it has targeted izicopan development in renal diseases, including atypical hemolytic uremic syndrome (aHUS), IgA nephropathy (IgAN) and C3 glomerulopathy (C3G), where early evidence exists for the role of C5a/C5aR inhibition and where izicopan’s favorable clinical profile could be a significant differentiator. InflaRx is currently in the planning stages for this development effort, with a goal of generating initial data from these open-label proof-of-concept studies in 2027.
Given the evolving regulatory environment surrounding the currently approved C5aR inhibitor, avacopan, InflaRx is evaluating the feasibility of multiple development approaches in AAV, including the potential for an expedited path to the commercial market in both the United States and Europe. Following the recommendation in June of the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) to revoke the marketing authorization for Tavneos in the EU, InflaRx announced it intends to engage with EMA regarding vilobelimab and izicopan to evaluate the path to approval in AAV in Europe, with a goal of establishing the most efficient development plan to bring the C5a/C5aR inhibition mechanism to patients. Together, vilobelimab and izicopan provide InflaRx with a complementary biologic and oral pipeline that is well positioned to address the evolving treatment landscape and significant unmet medical need in AAV.
In April 2026, InflaRx announced new in vitro findings demonstrating that izicopan does not exhibit time-dependent inhibition of CYP3A4, an important indicator for the risk for drug-drug interactions (DDIs) and liver toxicity. Further, in May 2026, the Company announced new pre-clinical data demonstrating lower reactive metabolite formation of izicopan in human liver microsomes versus the marketed comparator, avacopan. Reactive metabolite formation is widely used in drug development as an early mechanistic indicator of potential bioactivation-related safety risk. While in vitro findings do not directly predict clinical outcomes, InflaRx believes these results support izicopan’s differentiated profile as a potentially best-in-class oral C5a receptor (C5aR) inhibitor.
Furthermore, with the goal of generating proof-of-concept data in additional I&I indications as efficiently as possible, InflaRx intends to initiate a PK bridging study with izicopan in China this year to expedite subsequent proof-of-concept studies in China and elsewhere.
In May, InflaRx announced the pricing of an underwritten registered direct offering of 75,000,000 ordinary shares at an offering price of
Capital Markets Day
The Capital Markets Day planned for October 8 (morning ET) will feature updates on InflaRx’s development strategy for AAV as well as the potential of izicopan as a best-in-class therapy offering differentiated chemistry, metabolic properties, and potential safety advantages. Details regarding the precise timing, the anticipated agenda and speaker line-up are expected by early September.
Dr. Thomas Taapken, Chief Financial Officer of InflaRx, said: “InflaRx is on sound financial footing with a reinforced balance sheet and strongly differentiated pipeline assets. With a sufficient cash runway projected through 2029, we are well positioned to achieve multiple clinical milestones, including initiation of clinical studies with izicopan in AAV and additional renal diseases, as well as their respective data readouts.”
Financial Highlights – 2Q 2026
Sales and marketing expenses
Sales and marketing expenses for the six months ended June 30, 2026, decreased by
Research and development expenses
Research and development expenses for the six months ended June 30, 2026, decreased by
General and administrative expenses
General and administrative expenses decreased by
Other income
Other income decreased by
Net financial result
For the six months ended June 30, 2026, our net financial result decreased by
Net loss
For the six months ended June 30, 2026, and 2025, the Company incurred net losses of
Liquidity and capital resources
As of June 30, 2026, total funds available amounted to approximately
Net cash used in operating activities
Net cash used in operating activities increased to
Net cash from investing activities
Net cash from investing activities increased by
Net cash from financing activities
Net cash from financing activities increased by
InflaRx N.V. and subsidiaries
Unaudited consolidated statements of operations and comprehensive loss
for the six months ended June 30, 2026 and 2025
| For the three months ended June 30, | For the six months ended June 30, | ||||||||||||
| 2026 (unaudited) | 2025 (unaudited) | 2026 (unaudited) | 2025 (unaudited) | ||||||||||
| (in €, except for share data) | |||||||||||||
| Revenues | — | 39,432 | — | 39,432 | |||||||||
| Cost of sales | — | (2,399,583 | ) | — | (2,408,874 | ) | |||||||
| Gross profit (loss) | — | (2,360,151 | ) | — | (2,369,442 | ) | |||||||
| Sales and marketing expenses | (30,175 | ) | (1,013,347 | ) | (138,247 | ) | (2,471,326 | ) | |||||
| Research and development expenses | (4,739,126 | ) | (7,202,942 | ) | (8,909,671 | ) | (14,219,279 | ) | |||||
| General and administrative expenses | (2,548,319 | ) | (3,279,485 | ) | (5,725,763 | ) | (8,342,090 | ) | |||||
| Other income | 266,574 | 937,938 | 514,552 | 1,479,035 | |||||||||
| Other expenses | — | — | (66 | ) | (26 | ) | |||||||
| Operating result | (7,051,045 | ) | (12,917,988 | ) | (14,259,195 | ) | (25,923,127 | ) | |||||
| Finance income | 770,661 | 522,221 | 1,105,429 | 1,015,985 | |||||||||
| Finance expenses | (14,643 | ) | (3,355 | ) | (29,452 | ) | (7,441 | ) | |||||
| Foreign exchange result | 3,558,919 | (2,869,983 | ) | 4,051,301 | (4,778,812 | ) | |||||||
| Other financial result | (7,912,375 | ) | 852,834 | (7,109,214 | ) | 6,963,097 | |||||||
| Income taxes | — | — | — | — | |||||||||
| Income (loss) for the period | (10,648,484 | ) | (14,416,271 | ) | (16,241,132 | ) | (22,730,298 | ) | |||||
| Other comprehensive income (loss) that may be reclassified to profit or loss in subsequent periods: | |||||||||||||
| Exchange differences on translation of foreign currency | (19,274 | ) | (113,604 | ) | (34,301 | ) | (264,271 | ) | |||||
| Total comprehensive income (loss) | (10,667,758 | ) | (14,529,876 | ) | (16,275,433 | ) | (22,994,569 | ) | |||||
| Share information | |||||||||||||
| Weighted average number of shares outstanding | 117,663,937 | 67,747,130 | 95,103,732 | 65,542,269 | |||||||||
| Income (loss) per share (basic/diluted) | (0.09 | ) | (0.21 | ) | (0.17 | ) | (0.35 | ) | |||||
InflaRx N.V. and subsidiaries
Unaudited condensed consolidated statements of financial position
as of June 30, 2026 and December 31, 2025
| June 30, 2026 (unaudited) | December 31, 2025 | ||||
| (in €) | |||||
| ASSETS | |||||
| Non-current assets | |||||
| Property and equipment | 267,714 | 289,317 | |||
| Right-of-use assets | 802,608 | 861,667 | |||
| Intangible assets | 78,123 | 42,255 | |||
| Other assets | 126,201 | 151,198 | |||
| Financial assets | 237,020 | 237,373 | |||
| Total non-current assets | 1,511,667 | 1,581,810 | |||
| Current assets | |||||
| Current other assets | 2,331,968 | 3,261,038 | |||
| Other assets from government grants and research allowance | 2,997,282 | 2,487,763 | |||
| Tax receivables | 1,551,922 | 1,428,428 | |||
| Financial assets | 11,946,598 | 30,435,088 | |||
| Cash and cash equivalents | 146,567,894 | 16,022,171 | |||
| Total current assets | 165,395,665 | 53,634,487 | |||
| TOTAL ASSETS | 166,907,332 | 55,216,297 | |||
| EQUITY AND LIABILITIES | |||||
| Equity | |||||
| Issued capital | 17,684,187 | 8,675,143 | |||
| Share premium | 465,336,467 | 354,975,760 | |||
| Other capital reserves | 50,092,973 | 48,560,500 | |||
| Accumulated deficit | (394,067,134 | ) | (377,826,001 | ) | |
| Other components of equity | 7,137,079 | 7,171,379 | |||
| Total equity | 146,183,572 | 41,556,781 | |||
| Non-current liabilities | |||||
| Lease liabilities | 560,494 | 640,973 | |||
| Other liabilities | 36,877 | 36,877 | |||
| Total non-current liabilities | 597,371 | 677,850 | |||
| Current liabilities | |||||
| Trade and other payables | 5,303,862 | 5,399,383 | |||
| Lease liabilities | 272,685 | 256,943 | |||
| Employee benefits | 907,425 | 1,164,259 | |||
| Liabilities to warrant holders | 13,270,142 | 5,802,128 | |||
| Other liabilities | 372,275 | 358,954 | |||
| Total current liabilities | 20,126,389 | 12,981,666 | |||
| Total Liabilities | 20,723,760 | 13,659,516 | |||
| TOTAL EQUITY AND LIABILITIES | 166,907,332 | 55,216,297 | |||
InflaRx N.V. and subsidiaries
Unaudited condensed consolidated statements of changes in shareholders’ equity
for the six months ended June 30, 2026 and 2025
| (in €, except for share data) | Issued capital | Share premium | Other capital reserves | Accumulated deficit | Other components of equity | Total equity | ||||||||||||
| Balance as of January 1, 2026 | 8,675,143 | 354,975,760 | 48,560,500 | (377,826,001 | ) | 7,171,379 | 41,556,781 | |||||||||||
| Loss for the period | — | — | — | (16,241,132 | ) | — | (16,241,132 | ) | ||||||||||
| Exchange differences on translation of foreign currency | — | — | — | — | (34,301 | ) | (34,301 | ) | ||||||||||
| Total comprehensive loss | — | — | — | (16,241,132 | ) | (34,301 | ) | (16,275,433 | ) | |||||||||
| Issuance of ordinary shares | 9,000,000 | 118,442,651 | — | — | — | 127,442,651 | ||||||||||||
| Transaction costs for ordinary shares | — | (8,185,666 | ) | — | — | — | (8,185,666 | ) | ||||||||||
| Equity-settled share-based payments | — | — | 1,532,473 | — | — | 1,532,473 | ||||||||||||
| Share options exercised | 9,043 | 103,722 | — | — | — | 112,766 | ||||||||||||
| Balance as of June 30, 2026 | 17,684,186 | 465,336,467 | 50,092,973 | (394,067,133 | ) | 7,137,078 | 146,183,572 | |||||||||||
| Balance as of January 1, 2025 | 7,122,205 | 334,929,685 | 44,115,861 | (332,192,221 | ) | 7,440,510 | 61,416,039 | |||||||||||
| Loss for the period | — | — | — | (22,730,298 | ) | — | (22,730,298 | ) | ||||||||||
| Exchange differences on translation of foreign currency | — | — | — | — | (264,271 | ) | (264,271 | ) | ||||||||||
| Total comprehensive loss | — | — | — | (22,730,298 | ) | (264,271 | ) | (22,994,569 | ) | |||||||||
| Issuance of ordinary shares | 1,007,450 | 15,136,235 | — | — | — | 16,143,686 | ||||||||||||
| Transaction costs for ordinary shares | — | (1,109,305 | ) | — | — | — | (1,109,305 | ) | ||||||||||
| Equity-settled share-based payments | — | — | 3,588,514 | — | — | 3,588,514 | ||||||||||||
| Balance as of June 30, 2025 | 8,129,656 | 348,956,615 | 47,704,375 | (354,922,519 | ) | 7,176,239 | 57,044,364 | |||||||||||
InflaRx N.V. and subsidiaries
Unaudited condensed consolidated statements of cash flows
for the six months ended June 30, 2026 and 2025
| For the six months ended June 30, | |||||||
| 2026 (unaudited) | 2025 (unaudited) | ||||||
| (in €) | |||||||
| Operating activities | |||||||
| Loss for the period | (16,241,132 | ) | (22,730,298 | ) | |||
| Adjustments for: | |||||||
| Depreciation & amortization of property and equipment, right-of-use assets and intangible assets | 179,263 | 228,801 | |||||
| Net finance income | 1,981,937 | (3,192,828 | ) | ||||
| Share-based payment expense | 1,532,473 | 3,588,514 | |||||
| Net foreign exchange differences and other adjustments | 1,621,940 | 1,518,421 | |||||
| Changes in: | |||||||
| Other assets from government grants and research allowances | (509,519 | ) | (782,175 | ) | |||
| Other assets and trade receivables | 830,572 | (408,339 | ) | ||||
| Employee benefits | (256,834 | ) | (950,043 | ) | |||
| Other liabilities | 13,321 | 60,068 | |||||
| Trade and other payables | (95,521 | ) | (1,658,576 | ) | |||
| Inventories | — | 1,859,251 | |||||
| Interest received | 1,009,374 | 906,087 | |||||
| Interest paid | (30,100 | ) | (7,652 | ) | |||
| Net cash used in operating activities | (9,964,225 | ) | (21,568,767 | ) | |||
| Investing activities | |||||||
| Purchase of intangible assets, property and equipment | (45,919 | ) | (25,673 | ) | |||
| Purchase of current and non-current financial assets | (2,115,712 | ) | (35,514,042 | ) | |||
| Proceeds from sale of current financial assets | 21,154,151 | 28,288,912 | |||||
| Net cash from / (used in) investing activities | 18,992,521 | (7,250,803 | ) | ||||
| Financing activities | |||||||
| Proceeds from issuance of ordinary shares | 127,442,651 | 16,143,686 | |||||
| Proceeds from pre-funded warrants | — | 12,915,909 | |||||
| Transaction costs from issuance of ordinary shares and pre-funded warrants | (8,185,666 | ) | (1,949,998 | ) | |||
| Proceeds from exercise of share options | 112,766 | — | |||||
| Repayment of lease liabilities | (151,530 | ) | (199,904 | ) | |||
| Net cash from / (used in) financing activities | 119,218,221 | 26,909,693 | |||||
| Net increase/decrease in cash and cash equivalents | 128,246,517 | (1,909,878 | ) | ||||
| Effect of exchange rate changes on cash and cash equivalents | 2,299,207 | (3,462,651 | ) | ||||
| Cash and cash equivalents at beginning of period | 16,022,171 | 18,375,979 | |||||
| Cash and cash equivalents at end of period | 146,567,894 | 13,003,450 | |||||
About izicopan
Izicopan is an orally administered, small molecule inhibitor of the C5a receptor (C5aR) that has shown anti-inflammatory therapeutic effects in several pre-clinical disease models and in human studies. Further, in contrast to the marketed C5aR inhibitor, in vitro experiments demonstrated that izicopan does not exhibit time-dependent inhibition of cytochrome P450 3A4 (CYP3A4), which plays an important role in the metabolism of a variety of metabolites and drugs, including glucocorticoids. Izicopan has also demonstrated a favorable reactive metabolite profile in human liver microsomes. Reported results from a first-in-human study demonstrated that izicopan was well tolerated in treated subjects and exhibited no safety signals of concern in single doses ranging from 3 mg to 240 mg or multiple doses ranging from 30 mg once per day to 90 mg twice per day for 14 days. Pharmacokinetic / pharmacodynamic data support the best-in-class potential of izicopan, with a ≥
About vilobelimab
Vilobelimab is a first-in-class monoclonal anti-human complement factor C5a antibody which highly and effectively blocks the biological activity of C5a and demonstrates high selectivity towards its target in human blood. Thus, vilobelimab leaves the formation of the membrane attack complex (C5b-9) intact as an important defense mechanism of the innate immune system, which is not the case for molecules blocking C5. In pre-clinical studies, vilobelimab has been shown to control the inflammatory response-driven tissue and organ damage by specifically blocking C5a as a key “amplifier” of this response. Vilobelimab has been evaluated in two controlled Phase 2 AAV studies, the European IXCHANGE trial and the U.S. IXPLORE trial.
About InflaRx N.V.
InflaRx (Nasdaq: IFRX) is a biopharmaceutical company pioneering anti-inflammatory therapeutics by applying its proprietary anti-C5a and anti-C5aR technologies to discover, develop and commercialize highly potent and specific inhibitors of the complement activation factor C5a and its receptor, C5aR. C5a is a powerful inflammatory mediator involved in the progression of a wide variety of inflammatory diseases. InflaRx‘s lead program is izicopan, an orally administered small molecule inhibitor of C5a-induced signaling via the C5a receptor, which has shown promising PK/PD characteristics as well as therapeutic potential in Phase 1 and Phase 2a clinical studies. The Company is developing izicopan for the treatment of ANCA-associated vasculitis and additional renal diseases. InflaRx also has developed vilobelimab, a novel, intravenously delivered, first-in-class, anti-C5a monoclonal antibody that selectively binds to free C5a and has demonstrated disease-modifying clinical activity and tolerability in multiple clinical studies.
InflaRx was founded in 2007, and the group has offices and subsidiaries in Jena and Munich, Germany, as well as Ann Arbor, MI, USA. For further information, please visit www.inflarx.de. Follow InflaRx on LinkedIn. InflaRx GmbH (Germany) and InflaRx Pharmaceuticals Inc. (USA) are wholly owned subsidiaries of InflaRx N.V. (together, InflaRx).
Contacts:
| InflaRx N.V. | MC Services AG |
| Jan Medina, CFA Vice President, Head of Investor Relations Email: IR@inflarx.de | Katja Arnold, Laurie Doyle, Dr. Regina Lutz Email: inflarx@mc-services.eu Europe: +49 89-210 2280 U.S.: +1-339-832-0752 |
FORWARD-LOOKING STATEMENTS
This press release contains forward-looking statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “estimate,” “believe,” “predict,” “potential” or “continue,” among others. Forward-looking statements appear in a number of places throughout this release and may include statements regarding our intentions, beliefs, projections, outlook, analyses and current expectations concerning, among other things, the success of our future clinical trials for izicopan’s treatment of AAV and other renal diseases, including aHUS, IgAN and C3G, and our ability to establish proof of concept for izicopan across such indications; the timing, progress and results of preclinical studies and clinical trials of vilobelimab, izicopan and any other of our product candidates; our interactions with regulators regarding the results of clinical trials and potential regulatory approval pathways, including potential regulatory paths in AAV for vilobelimab and izicopan and related discussions with EMA; the timing and outcome of any discussions or submission of filings for regulatory approval of vilobelimab, izicopan or any other product candidate, and the timing of and our ability to obtain and maintain full regulatory approval and/or marketing authorization for any indication; potential strategic transactions or collaborations, including a potential partnership of izicopan or vilobelimab for PG; whether the FDA, EMA or any comparable foreign regulatory authority will accept or agree with the number, design, size, conduct or implementation of our clinical trials, including any proposed primary or secondary endpoints for such trials; our ability to leverage our proprietary anti-C5a and anti-C5aR technologies to discover and develop therapies to treat complement-mediated immunological and inflammatory diseases; our ability to protect, maintain and enforce our intellectual property protection for vilobelimab, izicopan and any other product candidates, and the scope of such protection; our manufacturing capabilities and strategy, including the scalability and cost of our manufacturing methods and processes, the optimization of our manufacturing methods and processes, and our ability to rely on existing third-party manufacturers or engage additional third-party manufacturers for planned future clinical trials and commercial supply; our estimates of our expenses, ongoing losses, future revenue, capital requirements and our needs for or ability to obtain additional financing; our ability to defend against liability claims resulting from the testing of our product candidates in the clinic or, if approved or authorized, any commercial sales; if any of our product candidates obtain regulatory approval or authorization, our ability to comply with and satisfy ongoing drug regulatory obligations and continued regulatory oversight; our ability to comply with enacted and future legislation in seeking marketing approval, authorization or commercialization; our future growth and ability to compete, which depends on our retaining key personnel and recruiting additional qualified personnel; our competitive position and the development of and projections relating to our competitors in the development of C5a and C5aR inhibitors and other therapeutic products being developed in similar medical conditions in which vilobelimab, izicopan or any other of our product candidates is being developed or our industry; and the risks, uncertainties and other factors described under the heading “Risk Factors” in our periodic filings with the SEC. These statements speak only as of the date of this press release and involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Given these risks, uncertainties and other factors, you should not place undue reliance on these forward-looking statements, and we assume no obligation to update these forward-looking statements, even if new information becomes available in the future, except as required by law.
