NEW YORK and LONDON, Nov. 15, 2018 (GLOBE NEWSWIRE) -- Akari Therapeutics, Plc (NASDAQ:AKTX), a biopharmaceutical company focused on innovative therapeutics to treat orphan autoimmune and inflammatory diseases where complement and or leukotriene systems are implicated, today announced its financial results for the third quarter ended September 30, 2018.
“We are focused on moving our four priority clinical programs forward and expect initial data from our trials in patients with bullous pemphigoid (BP) and atopic keratoconjunctivitis (AKC) in the first quarter of 2019,” commented Clive Richardson, Interim Chief Executive Officer of Akari Therapeutics.
Clinical development highlights and upcoming milestones
Third Quarter 2018 Financial Results
About Akari Therapeutics
Akari is a biopharmaceutical company focused on developing inhibitors of acute and chronic inflammation, specifically for the treatment of rare and orphan diseases, in particular those where the complement (C5) or leukotriene (LTB4) systems, or both complement and leukotrienes together, play a primary role in disease progression. Akari's lead drug candidate, Coversin, is a C5 complement inhibitor that also independently and specifically inhibits leukotriene B4 (LTB4) activity. Coversin is currently being clinically evaluated in four indications: bullous pemphigoid (BP), atopic keratoconjunctivitis (AKC), atypical hemolytic uremic syndrome (aHUS), and paroxysmal nocturnal hemoglobinuria (PNH). Akari believes that the dual action of Coversin on both C5 and LTB4 may be beneficial in AKC, BP, and aHUS. Akari is also developing other tick derived proteins, including longer acting versions.
Cautionary Note Regarding Forward-Looking Statements
Certain statements in this press release constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements reflect our current views about our plans, intentions, expectations, strategies and prospects, which are based on the information currently available to us and on assumptions we have made. Although we believe that our plans, intentions, expectations, strategies and prospects as reflected in or suggested by those forward-looking statements are reasonable, we can give no assurance that the plans, intentions, expectations or strategies will be attained or achieved. Furthermore, actual results may differ materially from those described in the forward-looking statements and will be affected by a variety of risks and factors that are beyond our control. Such risks and uncertainties for our company include, but are not limited to: needs for additional capital to fund our operations, our ability to continue as a going concern; uncertainties of cash flows and inability to meet working capital needs; an inability or delay in obtaining required regulatory approvals for Coversin and any other product candidates, which may result in unexpected cost expenditures; our ability to obtain orphan drug designation in additional indications; risks inherent in drug development in general; uncertainties in obtaining successful clinical results for Coversin and any other product candidates and unexpected costs that may result therefrom; difficulties enrolling patients in our clinical trials; failure to realize any value of Coversin and any other product candidates developed and being developed in light of inherent risks and difficulties involved in successfully bringing product candidates to market; inability to develop new product candidates and support existing product candidates; the approval by the FDA and EMA and any other similar foreign regulatory authorities of other competing or superior products brought to market; risks resulting from unforeseen side effects; risk that the market for Coversin may not be as large as expected; risks associated with the departure of our former Chief Executive Officers and other executive officers; risks related to material weaknesses in our internal controls over financial reporting and risks relating to the ineffectiveness of our disclosure controls and procedures; risks associated with the putative shareholder class action and SEC investigation; inability to obtain, maintain and enforce patents and other intellectual property rights or the unexpected costs associated with such enforcement or litigation; inability to obtain and maintain commercial manufacturing arrangements with third party manufacturers or establish commercial scale manufacturing capabilities; the inability to timely source adequate supply of our active pharmaceutical ingredients from third party manufacturers on whom the company depends; unexpected cost increases and pricing pressures and risks and other risk factors detailed in our public filings with the U.S. Securities and Exchange Commission, including our most recently filed Annual Report on Form 20-F filed with the SEC on July 18, 2018. Except as otherwise noted, these forward-looking statements speak only as of the date of this press release and we undertake no obligation to update or revise any of these statements to reflect events or circumstances occurring after this press release. We caution investors not to place considerable reliance on the forward-looking statements contained in this press release.
AKARI THERAPEUTICS, Plc | |||||||
CONDENSED CONSOLIDATED BALANCE SHEETS | |||||||
As of September 30, 2018 and December 31, 2017 | |||||||
(in U.S. Dollars, except share data) | |||||||
September 30, 2018 | December 31, 2017 | ||||||
Assets | (Unaudited) | ||||||
Current Assets: | |||||||
Cash | $ | 10,073,345 | $ | 28,106,671 | |||
Prepaid expenses and other current assets | 1,382,472 | 706,415 | |||||
Deferred Financing Costs | 585,000 | - | |||||
Total Current Assets | 12,040,817 | 28,813,086 | |||||
Restricted cash | 521,620 | 142,235 | |||||
Property and equipment, net | 29,955 | 55,898 | |||||
Patent acquisition costs, net | 34,839 | 39,124 | |||||
Total Assets | $ | 12,627,231 | $ | 29,050,343 | |||
Liabilities and Shareholders' Equity | |||||||
Current Liabilities: | |||||||
Accounts payable | $ | 1,404,496 | $ | 1,971,161 | |||
Accrued expenses | 1,710,693 | 4,795,873 | |||||
Liabilities related to options and warrants | 3,004,207 | 5,081,335 | |||||
Other current liabilities | 29,792 | - | |||||
Total Current Liabilities | 6,149,188 | 11,848,369 | |||||
Other long-term liabilities | 175,055 | 48,003 | |||||
Total liabilities | 6,324,243 | 11,896,372 | |||||
Commitments and Contingencies | |||||||
Shareholders' Equity: | |||||||
Share capital GBP of .01 par value | |||||||
Authorized: 10,000,000,000 ordinary shares; issued and outstanding: | |||||||
1,580,693,413 at September 30, 2018 and 1,525,693,393 at December 31, 2017, respectively | 23,651,277 | 22,927,534 | |||||
Additional paid-in capital | 106,239,087 | 104,799,550 | |||||
Accumulated other comprehensive loss | (296,483 | ) | (236,246 | ) | |||
Accumulated deficit | (123,290,893 | ) | (110,336,867 | ) | |||
Total Shareholders' Equity | 6,302,988 | 17,153,971 | |||||
Total Liabilities and Shareholders' Equity | $ | 12,627,231 | $ | 29,050,343 | |||
AKARI THERAPEUTICS, Plc | |||||||||||||
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS-UNAUDITED | |||||||||||||
For the Three and Nine Months Ended September 30, 2018 and September 30, 2017 | |||||||||||||
(in U.S. Dollars) | |||||||||||||
Nine Months Ended | Three Months Ended | ||||||||||||
September 30, 2018 | September 30, 2017 | September 30, 2018 | September 30, 2017 | ||||||||||
Operating Expenses: | |||||||||||||
Research and development costs | $ | 9,433,018 | $ | 16,167,426 | $ | 3,303,790 | $ | 6,382,542 | |||||
General and administrative expenses | 8,537,191 | 8,006,097 | 2,382,153 | 2,158,656 | |||||||||
Litigation settlement gain | (2,700,000 | ) | - | (2,700,000 | ) | - | |||||||
Total Operating Expenses | 15,270,209 | 24,173,523 | 2,985,943 | 8,541,198 | |||||||||
Loss from Operations | (15,270,209 | ) | (24,173,523 | ) | (2,985,943 | ) | (8,541,198 | ) | |||||
Other Income (Expense): | |||||||||||||
Interest income | 198,146 | 124,357 | 66,073 | 46,906 | |||||||||
Changes in fair value of option and warrant liabilities - (loss) gain | 2,077,128 | 1,010,005 | (715,846 | ) | (1,657,783 | ) | |||||||
Foreign currency exchange gain (loss) | 42,481 | (231,326 | ) | 36,036 | (218,274 | ) | |||||||
Other expenses (income) | (1,572 | ) | (10,615 | ) | 6,425 | (6,226 | ) | ||||||
Total Other Income (Expense) | 2,316,183 | 892,421 | (607,312 | ) | (1,835,377 | ) | |||||||
Net Loss | (12,954,026 | ) | (23,281,102 | ) | (3,593,255 | ) | (10,376,575 | ) | |||||
Other Comprehensive Loss: | |||||||||||||
Foreign Currency Translation Adjustment | (60,237 | ) | (8,302 | ) | (65,848 | ) | 85,428 | ||||||
Comprehensive Loss | $ | (13,014,263 | ) | $ | (23,289,404 | ) | $ | (3,659,103 | ) | $ | (10,291,147 | ) | |
Loss per common share (basic and diluted) | $ | (0.01 | ) | $ | (0.02 | ) | $ | (0.00 | ) | $ | (0.01 | ) | |
Weighted average common shares (basic and diluted) | 1,526,700,724 | 1,177,693,386 | 1,528,682,540 | 1,177,693,393 | |||||||||
For more information
Investor Contact:
Peter Vozzo
Westwicke Partners
(443) 213-0505
peter.vozzo@westwicke.com
Media Contact:
Mary-Jane Elliott / Sukaina Virji / Nicholas Brown
Consilium Strategic Communications
+44 (0)20 3709 5700
Akari@consilium-comms.com