Exhibit 99.1

 

InflaRx Reports Full Year 2022
Financial and Operating Results

● Major progress in development of vilobelimab

o Phase III study in PG announced following detailed feedback and recommendations from the U.S. Food and Drug Administration (FDA); clinical trial protocol submitted; first patient expected around mid-2023

o Fast Track and Orphan Drug designations granted for treatment of pyoderma gangrenosum (PG) in the United States and Orphan Drug designation granted in Europe

o Encouraging results from Phase III study in critically ill COVID-19 patients published in The Lancet Respiratory Medicine

o Emergency Use Authorization (EUA) application for treatment of critically ill, invasively mechanically ventilated COVID-19 patients submitted to the FDA; review ongoing

● First-in-human clinical trial with oral C5aR inhibitor INF904 initiated in November 2022; first data expected in H2 2023

● Amendment of co-development agreement with Staidson and incremental $2.5 million equity investment by Staidson HK for planned regulatory filing of BDB-001 for COVID-19 in China

● Total funds available approximately €83.7 million as of December 31, 2022, funding the company into H2 2025

Jena, Germany, March 22, 2023 – InflaRx N.V. (Nasdaq: IFRX), a clinical-stage biopharmaceutical company developing anti-inflammatory therapeutics by targeting the complement system, today announced financial and operating results for the year ended December 31, 2022.

Prof. Niels C. Riedemann, CEO and Founder of InflaRx, commented: “We are very pleased with the exceptional progress we have made in the past year with our lead drug candidate, vilobelimab, in several areas, as well as in advancing our pipeline with a new clinical asset, INF904, an orally available small molecule inhibitor of the C5a receptor. Upon detailed feedback from the FDA related to our development of vilobelimab for the treatment of PG, a rare debilitating and neutrophil driven skin disease, we have designed and submitted a Phase III protocol to the FDA while we are currently initiating the trial. We also submitted an EUA application to treat critically ill, mechanically ventilated patients with COVID-19, who today are still facing poor outcomes, and shortly await a decision from the FDA. Further, we expect first results from our ongoing Phase I clinical trial with INF904 and interim results from our Phase II clinical trial in cutaneous squamous cell carcinoma later this year. With these important milestones anticipated, 2023 promises to be an exciting year.”

 

Recent Highlights and R&D Update

InflaRx reported on key recent highlights and provided an update on its research and development activities.

Vilobelimab in Pyoderma Gangrenosum (PG)

Final data from an open-label, multi-center Phase IIa exploratory study evaluating the safety and efficacy of vilobelimab in patients with moderate to severe PG were presented in March 2022. The results showed a dose-dependent treatment effect. In the highest dose cohort of 2,400 mg, six out of seven patients demonstrated a clinical remission (Physician Global Assessment (PGA) score ≤ 1) and closure of the target ulcer.

Based on these compelling results and a productive End-of-Phase II meeting with the FDA in Q3 2022, InflaRx is moving forward with a pivotal Phase III clinical development program in this indication. In January 2023, the Company announced details related to the design of its planned Phase III study, a multi-national, randomized, double-blind, placebo-controlled trial. The Company has submitted the clinical trial protocol to the FDA and plans to begin patient enrollment around mid-2023.

Vilobelimab was granted Orphan Drug designation by both the FDA and the European Medicines Agency (EMA) for the treatment of ulcerative PG in June 2022, and in July was granted Fast Track designation for this indication by the FDA.

Vilobelimab for the Treatment of Critically ill COVID-19 Patients

InflaRx submitted an EUA application to the FDA for vilobelimab for the treatment of critically ill, intubated, mechanically ventilated COVID-19 patients in September 2022. The Company continues to be in active dialogue with and has addressed several requests for information that it received from the FDA. There is no set timeline for a decision from the FDA related to the EUA. The Company will continue to interact closely with the FDA and will provide a timely update when appropriate. If EUA is granted, InflaRx plans to seek full marketing authorization in major markets, including the United States and Europe and, in parallel, intends to seek partners to support commercialization efforts.

InflaRx also previously received Fast Track designation from the FDA for vilobelimab for the treatment of critically ill, intubated, mechanically ventilated COVID-19 patients.

In September 2022, results from the PANAMO Phase III study, an international, double-blind, placebo-controlled, randomized clinical trial investigating vilobelimab in invasively mechanically ventilated COVID-19 patients, were published in the peer-reviewed journal, The Lancet Respiratory Medicine, which included an in-depth statistical analysis supporting the robustness of the observed clinical survival benefit in the study.

Based on current COVID-19 trends, the U.S. Department of Health and Human Services (HHS) expects the COVID-19 federal public health emergency to expire on May 11, 2023. However, HHS has stated that it expects that the FDA will provide continued access to pathways for EUAs for medical products. See https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/faqs-what-happens-euas-when-public-health-emergency-ends.

In 2021, InflaRx was awarded a grant from the German Ministry of Education and Research and the German Ministry of Health to support the development of vilobelimab for the treatment of COVID-19. As of December 31, 2022, the Company had received €25.6 million in grant funds and still has a maximum amount of €15.9 million available for claiming under the grant throughout the end of the grant term in June 2023.

2

 

Vilobelimab in Cutaneous Squamous Cell Carcinoma (cSCC)

InflaRx is conducting an open-label, multicenter Phase II study, evaluating vilobelimab alone and in combination with pembrolizumab in patients with programmed cell death protein-1 (PD-1) or programmed cell death ligand-1 (PD-L1) inhibitor resistant/refractory, locally advanced or metastatic cSCC. Patients are being recruited into two independent arms - vilobelimab as monotherapy (Arm A) and in combination with pembrolizumab (Arm B). The main objectives of the trial are to assess the safety and antitumor activity of vilobelimab monotherapy and to determine the maximum tolerated or recommended dose, safety and antitumor activity in the combination arm in this patient population.

So far, 10 patients have been recruited into Arm A of the study. First data from an interim analysis in patients in Arm A is expected to be available in the first half of 2023. In Arm B of the study, as of today, 14 patients have been recruited into three dose cohorts (3+6+5). Data from an interim analysis in Arm B are expected to be available in the first half of 2024.

C5aR Inhibitor INF904

In November 2022, the company announced that the first healthy volunteer had been dosed in a randomized, double-blind, placebo-controlled Phase I trial. This single and multiple ascending dose Phase I trial aims to evaluate the safety, tolerability and pharmacokinetics of INF904 in healthy volunteers. The effect of INF904 on C5a-induced downstream activity will also be explored. Results are expected in the second half of 2023. In the future, InflaRx plans to develop INF904 for complement-mediated, chronic autoimmune and inflammatory diseases where oral administration is the preferred choice for patients.

Staidson Agreements

In December 2022, InflaRx amended its existing co-development agreement with Staidson (Beijing) BioPharmaceuticals Co., Ltd. (Staidson) from 2015 to support Staidson in its regulatory approval efforts for its proprietary drug candidate BDB-001 in China. InflaRx will receive royalties of 10% on net sales of BDB-001 for the treatment of COVID-19 in China. InflaRx has granted Staidson an exclusive license for use in China to certain of InflaRx’s clinical, manufacturing and regulatory documentation regarding vilobelimab in order to support and facilitate the planned regulatory filing for BDB-001 for the treatment of severely ill COVID-19 patients with the Chinese National Medical Products Administration (NMPA).

In parallel, InflaRx entered into a share purchase agreement with Staidson Hong Kong Investment Company Limited (Staidson HK), an affiliate of Staidson, pursuant to which Staidson HK purchased ordinary shares of InflaRx for an aggregate amount of $2.5 million at a price of $5.00 per share. The share purchase agreement also includes an option pursuant to which Staidson HK may in the future purchase, at InflaRx’s discretion, additional ordinary shares for an aggregate amount of $7.5 million.

2022 Financial Highlights

Dr. Thomas Taapken, CFO of InflaRx, said: “We are well financed to bring vilobelimab to patients, should we receive EUA, as well as to continue our development programs, including initiating a Phase III study in PG later this year. The grant money we have received from the German government for our COVID-19 development work as well as the investment by Staidson further strengthen our financial position, and we have sufficient cash to fund operations into H2 2025.”

3

 

Research and Development (R&D) Expenses

InflaRx’s R&D expenses increased by €1.8 million to €37.5 million in 2022, from €35.7 million in 2021. R&D expenses are predominantly comprised of costs for external contract research organizations (CROs) for pre-clinical activities and the conduct of clinical trials, costs for external contract manufacturing organizations (CMOs) for product manufacturing-related activities, costs for professional consultants primarily in the areas of regulatory affairs and intellectual property, as well as personnel expenses.

General and Administrative (G&A) Expenses

InflaRx’s G&A expenses increased by €2.9 million to €14.9 million in 2022, from €12.0 million in 2021. The increase is partly attributable to higher consulting and legal costs incurred in enhancing InflaRx’s internal control environment as it is complying with the auditor attestation requirement of Section 404(b) of the Sarbanes-Oxley Act of 2002 for the first time due to the loss of its “emerging growth company” status. G&A expenses are predominantly comprised of professional fees for auditors, consulting expenses not related to R&D activities, professional fees for lawyers, cost of facilities, travel, communication and office expenses as well as personnel related expenses.

Other Income

In 2022, InflaRx recognized other income of €20.1 million from grant payments received from the German federal government for the development of vilobelimab in COVID-19, including expenses related to clinical development and manufacturing process development.

Net Financial Result

InflaRx’s net financial result increased by €0.7 million to €2.7 million in 2022, from €2.0 million in 2021. This is mainly attributable to a net increase of €0.5 million in foreign exchange income and expense and an increase of €0.5 million in interest income from marketable securities.

Net Loss

InflaRx incurred a net loss of €29.5 million, or €0.67 per common share, in 2022 compared to €45.6 million, or €1.10 per common share, in 2021.

Liquidity and Capital Resources

As of December 31, 2022, InflaRx’s total funds available amounted to approximately €83.7 million, comprised of €16.3 million of cash and cash equivalents and €67.4 million of marketable securities.

Net Cash Used in Operating Activities

InflaRx’s net cash used in operating activities decreased to €33.7 million in 2022, from €39.9 million in 2021, mainly due to the decrease of loss before income tax resulting mainly from income recognized from the grant received from the German federal government.

Additional Financial Information

Additional information regarding these results and other relevant information is included in the notes to the financial statements in “Item 18. Financial Statements,” which are included in InflaRx’s most recent annual report on Form 20-F as filed with the U.S. Securities and Exchange Commission.

4

 

InflaRx N.V. and subsidiaries

Consolidated Statements of Operations and Comprehensive Loss for the Years Ended December 31, 2022, 2021 and 2020

in €, except for share information	2022			2021			2020
Operating Expenses
Research and development expenses		(37,526,090	)		(35,697,935	)		(25,684,140	)
General and administrative expenses		(14,869,564	)		(11,984,722	)		(8,467,203	)
Total Operating Expenses		(52,395,654	)		(47,682,657	)		(34,151,343	)
Other income		20,159,169			54,221			221,748
Other expenses		(1,381	)		(6,381	)		(13,209	)
Operating Result		(32,237,866	)		(47,634,817	)		(33,942,804	)
Finance income		608,679			109,391			887,702
Finance expenses		(45,250	)		(24,769	)		(26,000	)
Foreign exchange result		2,442,298			1,964,135			(776,512	)
Other financial result		(252,471	)		(44,000	)		(126,000	)
Income Taxes		—			—			—
Loss for the Period		(29,484,611	)		(45,630,059	)		(33,983,614	)
Share Information
Weighted average number of shares outstanding		44,207,873			41,629,974			27,064,902
Loss per share (basic/diluted)		(0.67	)		(1.10	)		(1.26	)
Loss for the Period		(29,484,611	)		(45,630,059	)		(33,983,614	)
Other comprehensive income (loss) that may be re-classified to profit or loss in subsequent periods:
Exchange differences on translation of foreign currency		4,206,810			6,777,061			(5,954,019	)
Total Comprehensive Loss		(25,277,801	)		(38,852,998	)		(39,937,633	)

5

 

InflaRx N.V. and subsidiaries

Consolidated Statements of Financial Position as December 31, 2022 and 2021

in €	2022			2021
ASSETS
Non-current assets
Property and equipment		328,920			274,373
Right-of-use assets		1,311,809			1,408,078
Intangible assets		138,905			235,216
Other assets		308,066			336,566
Financial assets		2,900,902			27,206,990
Total non-current assets		4,988,602			29,461,223
Current assets
Current other assets		14,170,510			10,983,458
Income tax receivable		1,432,087			1,282,177
Financial assets from government grants		732,971			—
Other Financial assets		64,810,135			57,162,266
Cash and cash equivalents		16,265,355			26,249,995
Total current assets		97,411,058			95,677,896
TOTAL ASSETS		102,399,660			125,139,120
EQUITY AND LIABILITIES
Equity
Issued capital		5,364,452			5,304,452
Share premium		282,552,633			280,310,744
Other capital reserves		36,635,564			30,591,209
Accumulated deficit		(243,460,290	)		(213,975,679	)
Other components of equity		7,257,081			3,050,270
Total equity		88,349,440			105,280,996
Non-current liabilities
Lease liabilities		987,307			1,066,354
Other liabilities		36,877			35,019
Total non-current liabilities		1,024,184			1,101,373
Current liabilities
Trade and other payables		4,987,538			8,574,244
Liabilities from government grants received		6,209,266			8,300,000
Lease liabilities		369,376			366,171
Employee benefits		1,312,248			1,378,130
Other liabilities		147,608			138,206
Total current liabilities		13,026,036			18,756,751
Total Liabilities		14,050,220			19,858,124
TOTAL EQUITY AND LIABILITIES		102,399,660			125,139,120

6

 

InflaRx N.V. and subsidiaries

Consolidated Statements of Changes in Shareholders’ Equity for the Years Ended December 31, 2022, 2021 and 2020

in €	Issued capital		Share premium			Other capital reserves		Accumulated deficit			Other components of equity			Total equity
Balance as of January 1, 2020		3,132,631		211,006,606			25,142,213		(134,362,006	)		2,227,228			107,146,673
Loss for the Period		—		—			—		(33,983,614	)		—			(33,983,614	)
Exchange differences on translation of foreign currency		—		—			—		—			(5,954,019	)		(5,954,019	)
Total Comprehensive Loss		—		—			—		(33,983,614	)		(5,954,019	)		(39,937,633	)
Issuance of common shares		234,982		9,535,961			—		—			—			9,770,943
Transaction costs		—		(729,840	)		—		—			—			(729,840	)
Equity-settled share-based payments		—		—			1,116,791		—			—			1,116,791
Share options exercised		19,797		477,149			—		—			—			496,946
Balance as of December 31, 2020		3,387,410		220,289,876			26,259,004		(168,345,620	)		(3,726,791	)		77,863,880
Loss for the Period		—		—			—		(45,630,059	)		—			(45,630,059	)
Exchange differences on translation of foreign currency		—		—			—		—			6,777,061			6,777,061
Total Comprehensive Loss		—		—			—		(45,630,059	)		6,777,061			(38,852,998	)
Issuance of common shares		1,873,203		63,269,346			—		—			—			65,142,549
Transaction costs		—		(4,219,222	)		—		—			—			(4,219,222	)
Equity-settled share-based payments		—		—			4,332,205		—			—			4,332,205
Share options exercised		43,839		970,744			—		—			—			1,014,583
Balance as of December 31, 2021		5,304,452		280,310,744			30,591,209		(213,975,679	)		3,050,270			105,280,996
Loss for the Period		—		—			—		(29,484,611	)		—			(29,484,611	)
Exchange differences on translation of foreign currency		—		—			—		—			4,206,810			4,206,810
Total Comprehensive Loss		—		—			—		(29,484,611	)		4,206,810			(25,277,801	)
Issuance of common shares		60,000		2,289,624			—		—			—			2,349,624
Transaction costs		—		(47,735	)		—		—			—			(47,735	)
Equity-settled share-based payments		—		—			6,044,356		—			—			6,044,356
Balance as of December 31, 2022		5,364,452		282,552,633			36,635,564		(243,460,290	)		7,257,080			88,349,440

7

 

InflaRx N.V. and subsidiaries

Consolidated Statements of Cash Flows for the Years ended December 31, 2022, 2021 and 2020

in €	2022			2021			2020
Operating activities
Loss for the Period		(29,484,611	)		(45,630,059	)		(33,983,614	)
Adjustments for:
Depreciation & amortization of property and equipment, right-of-use assets and intangible assets		596,597			669,434			712,713
Net finance income		(2,753,255	)		(2,004,757	)		40,810
Share-based payment expense		6,044,356			4,332,205			1,116,791
Net foreign exchange differences		385,359			111,606			(247,322	)
Other non-cash adjustments		—			—			3,436
Changes in:
Financial assets from government grants		(732,971	)		—			—
Other assets		(3,308,485	)		(7,094,467	)		(1,554,611	)
Employee benefits		(64,024	)		(3,290	)		355,545
Other liabilities		9,403			19,863			8,960
Liabilities from government grants received		(2,090,734	)		8,300,000			—
Trade and other payables		(3,586,706	)		316,112			(4,155,529	)
Interest received		1,287,200			1,070,235			1,201,547
Interest paid		(44,946	)		(23,633	)		(26,387	)
Net cash used in operating activities		(33,742,817	)		(39,936,751	)		(36,527,661	)
Investing activities
Purchase of intangible assets and property and equipment		(162,391	)		(37,778	)		(94,189	)
Purchase of non-current other financial assets		—			—			—
Purchase of current and non-current financial assets		(64,474,543	)		(97,516,417	)		(101,600,176	)
Proceeds from the maturity of current financial assets		83,995,029			71,603,310			123,056,347
Net cash from/ (used in) investing activities		19,358,095			(25,950,885	)		21,361,982
Financing activities
Proceeds from issuance of common shares		2,349,624			65,142,549			9,770,944
Transaction costs from issuance of common shares		(47,735	)		(4,219,222	)		(729,841	)
Proceeds from exercise of share options		—			1,014,583			496,946
Repayment of lease liabilities		(364,429	)		(360,644	)		(366,156	)
Net cash from/ (used in) financing activities		1,937,459			61,577,266			9,171,893
Net increase/(decrease) in cash and cash equivalents		(12,447,262	)		(4,310,369	)		(5,993,786	)
Effect of exchange rate changes on cash and cash equivalents		2,462,622			4,591,683			(1,168,813	)
Cash and cash equivalents at beginning of period		26,249,995			25,968,681			33,131,280
Cash and cash equivalents at end of period		16,265,355			26,249,995			25,968,681

8

 

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 controlled the inflammatory response driven tissue and organ damage by specifically blocking C5a as a key “amplifier” of this response. Vilobelimab has been shown to be well tolerated within clinical trials in different disease settings. Vilobelimab is being developed for various debilitating or life-threatening inflammatory indications, including pyoderma gangrenosum (PG), severe COVID-19 and cutaneous squamous cell carcinoma (cSCC).

The COVID-19 related work described herein is partly funded by the German Federal Government through grant number 16LW0113 (VILO-COVID). All responsibility for the content of this work lies with InflaRx.

About InflaRx N.V.:

InflaRx (Nasdaq: IFRX) is a clinical-stage biopharmaceutical company focused on applying its proprietary anti-C5a and C5aR technologies to discover and develop first-in-class or best-in-class, potent and specific inhibitors of C5a and C5aR. Complement C5a and its receptor C5aR are powerful inflammatory mediators involved in the progression of a wide variety of autoimmune and other inflammatory diseases. 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.

Contacts:

InflaRx N.V.

Email: IR@inflarx.de

MC Services AG

Katja Arnold, Laurie Doyle, Dr. Regina Lutz
Email: inflarx@mc-services.eu
Europe: +49 89-210 2280
US: +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,” “believe,” “estimate,” “predict,” “potential” or “continue” and similar expressions. Forward-looking statements appear in a number of places throughout this release and may include statements regarding the Company’s intentions, beliefs, projections, outlook, analyses and current expectations concerning, among other things, the status of the Company’s EUA application for vilobelimab to treat critical COVID-19 and the FDA’s review of such application; the Company’s ongoing and planned pre-clinical development and clinical trials, including the development of vilobelimab in several indications; the Company’s interactions with regulators regarding the results of clinical trials, clinical trial design and potential regulatory approval pathways; the impact of the COVID-19 pandemic on the Company; the timing and its ability to commence and conduct clinical trials; potential results from current or potential future collaborations; its ability to make regulatory filings, obtain positive guidance from regulators, and obtain and maintain regulatory approvals for its product candidates; its intellectual property position; its ability to develop commercial functions; expectations regarding clinical trial data; decisions regarding the strategic direction of the Company; its results of operations, cash needs, financial condition, liquidity, prospects, future transactions, growth and strategies; the industry in which the Company operates; the trends that may affect the industry or the Company’s business; and the risks, uncertainties and other factors described under the heading “Risk Factors” in Company’s periodic filings with the U.S. Securities and Exchange Commission. 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 the Company’s 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 the Company assumes no obligation to update these forward-looking statements, even if new information becomes available in the future, except as required by law.

9