|Bid||3.9900 x 3200|
|Ask||4.0300 x 1000|
|Day's Range||3.9000 - 4.1200|
|52 Week Range||2.5200 - 9.6980|
|Beta (5Y Monthly)||0.50|
|PE Ratio (TTM)||N/A|
|Earnings Date||Oct 29, 2020|
|Forward Dividend & Yield||N/A (N/A)|
|1y Target Est||9.21|
Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
* Initiated Phase III part of the Phase II/III adaptive, randomized, controlled trial in patients with severe COVID-19 induced pneumonia * Published encouraging data from Phase II part of COVID-19 trial in The Lancet Rheumatology * Announced leadership team additions * Cash, cash equivalents and financial assets of approximately €95.7 million as of September 30, 2020JENA, Germany, Oct. 29, 2020 (GLOBE NEWSWIRE) -- InflaRx (Nasdaq: IFRX), a clinical-stage biopharmaceutical company developing anti-inflammatory therapeutics by targeting the complement system, announced today financial results for the three and nine months ended September 30, 2020.“With cases of COVID-19 on the rise throughout the world, there remains an urgent need to find safe and efficacious treatments for critically ill patients. Thus, we are highly focused on advancing our ongoing Phase III trial with IFX-1 in patients with severe COVID-19 induced pneumonia,” said Prof. Niels C. Riedemann, Chief Executive Officer and Founder of InflaRx. “In addition, we are continuing to move forward IFX-1 in development for important inflammatory indications, including hidradenitis suppurativa, pyoderma gangraenosum and ANCA-associated vasculitis, all disease areas where patients are in need of better treatment options.”Corporate and R&D Highlights * Leadership appointments: In September 2020, InflaRx announced the appointment of Thomas Taapken, Ph.D. as Chief Financial Officer, and Jordan Zwick was promoted to the newly created position of Chief Strategy Officer. * IFX-1 in COVID-19 induced pneumonia: In September 2020, InflaRx announced the start of the global Phase III part of its Phase II/III trial with IFX-1 in severe COVID-19 induced pneumonia with the initiation of the first clinical site in the Netherlands. In parallel, the German regulatory authority, the Paul-Ehrlich-Institut (PEI), approved the Phase III clinical trial in Germany. The trial is currently enrolling, and patients are undergoing treatment. The randomized, double-blinded and placebo-controlled Phase III part of the Phase II/III trial is planned to enroll approximately 360 early intubated, critically ill patients with COVID-19 induced pneumonia across sites in the US, EU, South America and other regions. Patients are being randomized 1:1 to receive either IFX-1 or placebo; all patients will receive standard of care. The primary endpoint is 28-day all-cause mortality; key secondary endpoints will include assessment of organ support and disease improvement. An interim analysis is planned after enrollment of 180 patients, with a potential for an early stop for efficacy or futility. Also in September, encouraging data from the Phase II part of the study were published in the peer-reviewed journal, The Lancet Rheumatology. * IFX-1 in Hidradenitis Suppurativa (HS): The Company is assessing different strategies for a potential pathway to regulatory approval for IFX-1 in the United States and plans to engage with the Food & Drug Administration (FDA) on next steps. In Europe, InflaRx is working diligently to address the feedback received in Scientific Advice from the European Medicines Agency (EMA) and analyzing the strategy for its Phase III development program for the use of IFX-1 in the treatment of HS. * IFX-1 in Pyoderma Gangraenosum (PG): The Phase IIa open label trial continues to enroll patients in the higher dose groups. Additional clinical trial sites continue to be opened to support enrollment. Results from the higher dose groups are expected in 2021. * IFX-1 in ANCA-associated vasculitis (AAV): In the US IXPLORE study, all patients have completed treatment. Data is expected in the first half of 2021. In the European Phase II IXCHANGE trial, Part 2 continues to enroll patients, with approximately half of the targeted 25 patients enrolled. Final results are expected in 2021. * IFX-1 in oncology: Activities are ongoing for the Phase IIa oncology program, with expected initiation in the first half of 2021.Financial highlights – Q3 2020Research and development expenses incurred for the nine months ended September 30, 2020 decreased over the corresponding period in 2019 by €13.7 million. This decline was primarily due to lower contribution of expense in the period from the Phase IIb clinical development of IFX-1 in HS since this study was completed in 2019, offset by the COVID-19 trial expenses. These two factors led to €6.6 million of lower manufacturing costs which contributed to an overall decline in third-party expenses of €11.5 million. The €2.0 million decrease in personnel expenses is mainly caused by equity-settled share-based compensation.General and administrative expenses decreased by €3.4 million to €6.1 million for the nine months ended September 30, 2020, from €9.4 million for the nine months ended September 30, 2019. This decrease is largely attributable to lower expenses associated with equity-settled share-based compensation recognized in personnel expenses (€3.0 million). Furthermore, legal, consulting and other expenses decreased by €0.4 million to €3.2 million for the nine months ended September 30, 2020, from €3.6 million for the nine months ended September 30, 2019. In 2019, consulting expenses were higher due to a one-time strategic project in June 2019. Other expenses in 2020 include increased D&O insurance costs compared to the respective nine month period in 2019.Net financial result decreased by €2.7 million to €0.6 million for the nine months ended September 30, 2020, from €3.3 million for the nine months ended September 30, 2019. This decrease is mainly attributable to higher foreign exchange losses, which increased by €1.7 million partially compensated with foreign exchange gains (€0.5 million) while interest on marketable securities declined by €1.5 million.Net loss for the nine months ended September 30, 2020 was €25.1 million , compared to €39.6 million for the nine months ended September 30, 2019. On September 30, 2020, the Company’s total funds available were approximately €95.7 million, composed of cash and cash equivalents (€44.8 million) and financial assets (€50.8 million).Net cash used in operating activities decreased to €26.8 million in the nine months ended September 30, 2020, from €27.0 million in the nine months ended September 30, 2019. The decrease of cash expenses, such as third-party expenses for manufacturing and clinical trials for our lead program IFX-1 was nearly offset by €12.3 million lower payments on trade liabilities in the nine months ended September 30, 2019.Additional information regarding these results and other relevant information is included in the notes to the unaudited Condensed Consolidated Financial Statements as of September 30, 2020, as well as the financial statements as of December 31, 2019 in “ITEM 18. Financial statements,” which is included in InflaRx’s Annual Report on Form 20-F as filed with the U.S. Securities and Exchange Commission (SEC).InflaRx N.V. and subsidiaries Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss for the three and nine months ended September 30, 2020 and 2019 For the three months ended September 30,For the nine months ended September 30, (in €, except for share data)2020 (unaudited) 2019 (unaudited) 2020 (unaudited) 2019 (unaudited) Operating Expenses Research and development expenses(5,246,536) (13,405,646) (19,901,661) (33,598,018) General and administrative expenses(1,166,070) (2,490,245) (6,057,767) (9,439,080) Total Operating Expenses(6,412,606) (15,895,891) (25,959,428) (43,037,098) Other income3,471 126,559 200,763 194,261 Other expenses(13) (838) (9,184) (83,907) Operating Result(6,409,148) (15,770,170) (25,767,849) (42,926,744) Finance income1,325,367 2,029,992 3,593,803 4,527,952 Finance expenses(1,775,183) (761,268) (2,951,147) (1,211,366) Net Financial Result(449,816) 1,268,725 642,656 3,316,586 Loss for the Period(6,858,964) (14,501,446) (25,125,193) (39,610,157) Share Information Weighted average number of shares outstanding27,733,778 25,982,754 26,674,233 25,970,571 Loss per share (basic/diluted)(0.25) € (0.56) (0.94) € (1.53) Loss for the Period(6,858,964) (14,501,446) (25,125,193) (39,610,157) Other comprehensive income (loss) that may be reclassified to profit or loss in subsequent periods: Exchange differences on translation of foreign currency(3,022,687) 4,988,141 (2,761,792) 5,683,610 Total Comprehensive Loss(9,881,651) (9,513,305) (27,886,985) (33,926,548) InflaRx N.V. and subsidiaries Unaudited Condensed Consolidated Statements of Financial Position as of September 30, 2020 and December 31, 2019in €September 30, 2020 (unaudited) December 31, 2019 ASSETS Non-current assets Property, plant and equipment467,937 576,373 Right-of-use assets623,452 836,924 Intangible assets379,811 452,400 Other assets385,837 452,217 Financial assets272,448 272,614 Total non-current assets2,129,485 2,590,528 Current assets Other assets3,794,075 3,500,884 Financial assets50,563,814 82,353,867 Cash and cash equivalents44,834,089 33,131,280 Total current assets99,191,977 118,986,031 TOTAL ASSETS101,321,462 121,576,558 EQUITY AND LIABILITIES Equity Issued capital3,387,410 3,132,631 Share premium220,289,876 211,006,606 Other capital reserves26,039,651 25,142,213 Accumulated deficit(159,487,199) (134,362,006) Other components of equity(534,564) 2,227,228 Total equity89,695,174 107,146,673 Non-current liabilities Lease liabilities123,053 330,745 Other non-financial liabilities35,488 39,013 Total non-current liabilities158,541 369,758 Current liabilities Trade and other payables9,998,452 12,413,662 Lease liabilities511,652 515,203 Employee benefits799,812 975,629 Social security, other taxes and other non-financial liabilities121,830 105,634 Provisions36,000 50,000 Total current liabilities11,467,747 14,060,128 Total Liabilities11,626,288 14,429,886 TOTAL EQUITY AND LIABILITIES101,321,462 121,576,558 InflaRx N.V. and subsidiaries Unaudited Condensed Consolidated Statements of Changes in Shareholders’ Equity for the nine months ended September 30, 2020 and 2019(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, 20203,132,631 211,006,606 25,142,213 (134,362,006) 2,227,228 107,146,673 Loss for the period— — — (25,125,193) — (25,125,193) Exchange differences on translation of foreign currency— — — — (2,761,792) (2,761,792) Total comprehensive loss— — — (25,125,193) (2,761,792) (27,886,985) Contributions Issuance of common shares234,982 9,535,961 — — — 9,770,943 Transaction costs— (729,841) — — — (729,841) Equity-settled share-based payments— — 897,438 — — 897,438 Share options exercised19,797 477,149 — — — 496,946 Total Contributions254,779 9,283,269 897,438 — — 10,435,486 Balance as of September 30, 20203,387,410 220,289,876 26,039,651 (159,487,199) (534,564) 89,695,174 Balance as of January 1, 20193,115,725 211,021,835 18,310,003 (81,107,188) 50,196 151,390,571 Loss for the period— — — (39,610,157) — (39,610,157) Exchange differences on translation of foreign currency— — — — 5,683,610 5,683,610 Total comprehensive loss— — — (39,610,157) 5,683,610 (33,926,547) Contributions Equity-settled share-based pay-ments— — 5,689,367 — — 5,689,367 Share options exercised16,905 (15,229) — — — 1,676 Total Contributions16,905 (15,229) 5,689,367 — — 5,691,043 Balance as of September 30, 20193,132,631 211,006,606 23,999,370 (120,717,345) 5,733,805 123,155,067 InflaRx N.V. and subsidiaries Unaudited Condensed Consolidated Statements of Cash Flows for the nine months ended September 30, 2020 and 2019in €For the nine months ended September 30, 2020 (unaudited) For the nine months ended September 30, 2019 (unaudited) Operating activities Loss for the period(25,125,193) (39,610,157) Adjustments for: Depreciation & amortization of property, plant, equipment, right-of-use assets and intangible assets533,687 485,822 Net financial result(642,656) (3,316,586) Share-based payment expense897,438 5,689,367 Net foreign exchange differences(869,402) (345,347) Other non-cash adjustments— 59,958 Changes in: Other assets(226,811) (1,233,165) Employee benefits(191,042) (14,316) Social security and other current non-financial liabilities13,896 (205,175) Trade and other payables(2,415,210) 9,859,875 Interest received1,238,643 1,653,617 Interest paid(15,546) (19,822) Net cash used in operating activities(26,802,196) (26,995,930) Investing activities Purchase of intangible assets, laboratory and office equipment(83,855) (622,265) Purchase of non-current other financial assets— (75,543) Purchase of current financial assets(68,169,518) 40,539,826 Proceeds from the maturity of financial assets97,465,290 (42,688,210) Net cash from/ (used in) investing activities29,211,918 (2,846,193) Financing activities Proceeds from issuance of common shares9,770,944 — Transaction costs from issuance of common shares(729,841) — Proceeds from exercise of share options496,946 1,676 Repayment of lease liabilities(275,323) (209,176) Net cash from/ (used in) financing activities9,262,726 (207,500) Net increase/(decrease) in cash and cash equivalents11,672,447 (30,049,623) Effect of exchange rate changes on cash and cash equivalents30,362 1,673,191 Cash and cash equivalents at beginning of period33,131,280 55,386,240 Cash and cash equivalents at end of period44,834,089 27,009,808 About IFX-1:IFX-1 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, IFX-1 leaves the formation of the membrane attack complex (C5b-9) intact as an important defense mechanism, which is not the case for molecules blocking the cleavage of C5. IFX-1 has been demonstrated to control the inflammatory response driven tissue and organ damage by specifically blocking C5a as a key “amplifier” of this response in pre-clinical studies. IFX-1 is believed to be the first monoclonal anti-C5a antibody introduced into clinical development. Approximately 300 people have been treated with IFX-1 in clinical trials, and the antibody has been shown to be well tolerated. IFX-1 is currently being developed for various indications, including Hidradenitis Suppurativa, ANCA-associated vasculitis, Pyoderma Gangraenosum and COVID-19 pneumonia.About InflaRx N.V.:InflaRx (Nasdaq: IFRX) is a clinical-stage biopharmaceutical company focused on applying its proprietary anti-C5a technology to discover and develop first-in-class, potent and specific inhibitors of C5a. Complement C5a is a powerful inflammatory mediator 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.com.Contacts:InflaRx N.V.Jordan Zwick – Chief Strategy Officer Email: email@example.com Tel: +1 917-338-6523MC Services AGKatja Arnold, Laurie Doyle, Andreas Jungfer Email: firstname.lastname@example.org Europe: +49 89-210 2280 US: +1-339-832-0752FORWARD-LOOKING STATEMENTSThis 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 our intentions, beliefs, projections, outlook, analyses and current expectations concerning, among other things, our ongoing and planned preclinical development and clinical trials; the impact of the COVID-19 pandemic on the Company; the timing and our ability to commence and conduct clinical trials; potential results from current or potential future collaborations; our ability to make regulatory filings, obtain positive guidance from regulators, and obtain and maintain regulatory approvals for our product candidates; our intellectual property position; our ability to develop commercial functions; expectations regarding clinical trial data; our results of operations, cash needs, financial condition, liquidity, prospects, future transactions, growth and strategies; the industry in which we operate; the trends that may affect the industry or us and the risks uncertainties and other factors described under the heading “Risk Factors” in InflaRx’s periodic filings with the 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 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.
Shares in InflaRx closed 6% higher on Tuesday after Phase 2 data showed that its monoclonal antibody IFX-1 therapeutic tested in adults with Covid-19 induced pneumonia appears safe and has “promising” parameters.The exploratory Phase 2 results demonstrated that inhibition with InflaRx’s (IFRX) IFX-1 appears safe in adults with severe COVID-19, according to the data published in The Lancet.“FX-1 treatment had a positive, but not significant, effect on reversal of blood lymphocytopenia and reduction in lactate dehydrogenase concentrations - two parameters that have been reported as biomarkers for COVID-19 disease severity,” according to the data analysis.IFX-1 is a first-in-class monoclonal anti-human complement factor C5a antibody, which blocks the biological activity of C5a and demonstrates high selectivity towards its target in human blood. IFX-1 demonstrated to control the inflammatory response driven tissue and organ damage by specifically blocking C5a as a key “amplifier” of this response in pre-clinical studies.According to the Lancet report, the expert committee, based on the review of available data, unanimously recommended continuing into Phase 3 and advised on changes to the study protocol.However, it was also cautioned that ultimately, the Phase 2 part of the trial was exploratory in nature and efficacy of IFX-1 in patients with Covid-19 must be confirmed in a separate Phase 3 trial.On Sept. 13, InflaRx announced the start of the global Phase 3 part of its Phase 2/3 trial with IFX-1 in severe Covid-19 induced pneumonia with the initiation of the first clinical site in the Netherlands. The Phase 3 trial will enroll approximately 360 early intubated, critically ill patients with Covid-19 induced pneumonia across sites in the US, EU, South America and other regions.The primary endpoint will be 28-day all-cause mortality. Key secondary endpoints will include assessment of organ support and disease improvement. An interim analysis is planned after enrolment of 180 patients, with a potential for an early stop for efficacy or futility. In parallel, the German regulatory authority, the Paul-Ehrlich-Institut (PEI), has approved the Phase 3 clinical trial in Germany.Shares in InflaRx have already advanced 15% so far this year, with the $9.83 average analyst price target implying a whopping 114% upside potential lies ahead.Commenting on the data, Leerink Partners analyst Joseph Schwartz said that he is "encouraged" by the "strong signals" in the Phase 2 data and the Phase 3 trial design. For now, Schwartz is sticking to his Hold rating on the stock, while he is awaiting continued development in this indication.The rest of the Street is sidelined on the stock. The Hold analyst consensus breaks down into 2 Holds, 1 Sell versus 1 Buy. (See IFRX stock analysis on TipRanks)Related News: Inovio Dives 28% After FDA Halts COVID-19 Vaccine Trial Bausch Scores FDA Approval For Preservative Free Allergy Eyedrop Aquestive Plunges 37% As FDA Rejects Seizure Drug; Street Stays Bullish More recent articles from Smarter Analyst: * Papa John's Up 3% On September, Q3 Comps Update * Ford Slashes Mustang EV Pricing Ahead Of Deliveries – Report * Coca-Cola, Molson Coors Team Up For US Topo Chico Alcoholic Drink * Nvidia, VMware Partner To Ease AI Use For Enterprises