La Jolla Pharmaceutical Company (NASDAQ: LJPC) (the Company or La Jolla), a leader in the development of innovative therapies intended to significantly improve outcomes in patients suffering from life-threatening diseases, today reported financial results for the three and nine months ended September 30, 2017 and highlighted recent corporate progress.
Recent Corporate Progress
“The first nine months of 2017 have been exciting for La Jolla, highlighted by the positive results from ATHOS-3, the publication of these results in The New England Journal of Medicine and the FDA acceptance of our NDA for LJPC-501,” said George Tidmarsh, M.D., Ph.D., President and Chief Executive Officer of La Jolla. “We look forward to building on this momentum with the preparation for the potential commercial launch of LJPC-501, if approved by the FDA, and the initiation of our pivotal study of LJPC-401 in beta thalassemia patients suffering from iron overload.”
Results of Operations
As of September 30, 2017, the Company had $120.8 million in cash and cash equivalents, compared to $65.7 million of cash and cash equivalents at December 31, 2016. Cash used in operating activities for the nine months ended September 30, 2017 was $60.4 million, compared to $40.1 million for the same period in 2016. Net loss for the three and nine months ended September 30, 2017 was $26.3 million and $76.3 million, or $1.19 per share and $3.65 per share, respectively, compared to a net loss of $21.3 million and $53.3 million, or $1.23 per share and $3.10 per share, respectively, for the same periods in 2016.
About La Jolla Pharmaceutical Company
La Jolla Pharmaceutical Company is a biopharmaceutical company focused on the discovery, development and commercialization of innovative therapies intended to significantly improve outcomes in patients suffering from life-threatening diseases. The Company has several product candidates in development. LJPC-501 is La Jolla’s proprietary formulation of synthetic human angiotensin II for the potential treatment of hypotension in adult patients with distributive or vasodilatory shock who remain hypotensive despite fluid and vasopressor therapy. LJPC-401 is La Jolla’s proprietary formulation of synthetic human hepcidin for the potential treatment of conditions characterized by iron overload, such as hereditary hemochromatosis, beta thalassemia, sickle cell disease and myelodysplastic syndrome. For more information on La Jolla, please visit www.ljpc.com.
Forward Looking Statement Safe Harbor
This press release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements relate to future events or the Company’s future results of operations. These statements are only predictions or statements of current expectations and involve known and unknown risks, uncertainties and other factors that may cause actual results to be materially different from those anticipated by the forward-looking statements. The Company cautions readers not to place undue reliance on any such forward-looking statements, which speak only as of the date they were made. Certain of these risks, uncertainties and other factors are described in greater detail in the Company’s filings with the U.S. Securities and Exchange Commission (SEC), all of which are available free of charge on the SEC’s web site www.sec.gov. These risks include, but are not limited to, risks relating to: the timing and prospects for approval of LJPC-501 by the FDA, EMA and other regulatory authorities; risks relating to the scope of product labels (if approved); potential market sizes; the anticipated timing for regulatory actions; the impact of pharmaceutical industry regulation and health care legislation in the Europe and the United States; the anticipated timing for regulatory actions; the success of future development activities; potential indications for which the Company’s product candidates may be developed; and the expected duration over which the Company’s cash balances will fund its operations. Subsequent written and oral forward-looking statements attributable to the Company or to persons acting on its behalf are expressly qualified in their entirety by the cautionary statements set forth in the Company’s reports filed with the SEC. The Company expressly disclaims any intent to update any forward-looking statements.
LA JOLLA PHARMACEUTICAL COMPANY |
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Unaudited Condensed Consolidated Statements of Operations | ||||||||||||||||
(in thousands, except per share amounts) |
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Three Months Ended September 30, |
Nine Months Ended
September 30, |
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2017 | 2016 | 2017 | 2016 | |||||||||||||
Revenue | ||||||||||||||||
Contract revenue - related party | $ | — | $ | 44 | $ | — | $ | 531 | ||||||||
Total revenue | — | 44 | — | 531 | ||||||||||||
Expenses | ||||||||||||||||
Research and development | 19,093 | 16,992 | 57,666 | 42,111 | ||||||||||||
General and administrative | 7,390 | 4,349 | 18,915 | 11,868 | ||||||||||||
Total expenses | 26,483 | 21,341 | 76,581 | 53,979 | ||||||||||||
Loss from operations | (26,483 | ) | (21,297 | ) | (76,581 | ) | (53,448 | ) | ||||||||
Other income, net | 195 | 46 | 324 | 150 | ||||||||||||
Net loss | $ | (26,288 | ) | $ | (21,251 | ) | $ | (76,257 | ) | $ | (53,298 | ) | ||||
Basic and diluted net loss per share | $ | (1.19 | ) | $ | (1.23 | ) | $ | (3.65 | ) | $ | (3.10 | ) | ||||
Weighted-average common shares outstanding - basic and diluted | 22,125 | 17,211 | 20,900 | 17,211 | ||||||||||||
LA JOLLA PHARMACEUTICAL COMPANY | ||||||||
Condensed Consolidated Balance Sheets | ||||||||
(in thousands, except share and par value amounts) |
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September 30, |
December 31, |
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(Unaudited) | ||||||||
ASSETS | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 120,840 | $ | 65,726 | ||||
Restricted cash | 911 | 200 | ||||||
Prepaid expenses and other current assets | 1,772 | 1,505 | ||||||
Total current assets | 123,523 | 67,431 | ||||||
Property and equipment, net | 6,534 | 3,145 | ||||||
Other assets | — | 219 | ||||||
Total assets | $ | 130,057 | $ | 70,795 | ||||
LIABILITIES AND SHAREHOLDERS’ EQUITY | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 6,239 | $ | 6,652 | ||||
Accrued clinical and other expenses | 795 | 1,029 | ||||||
Accrued payroll and related expenses | 3,228 | 2,077 | ||||||
Total current liabilities | 10,262 | 9,758 | ||||||
Shareholders’ equity: | ||||||||
Common Stock, $0.0001 par value; 100,000,000 shares authorized, 22,145,243 and 18,261,557 shares issued and outstanding at September 30, 2017 and December 31, 2016, respectively | 2 | 2 | ||||||
Series C-12 Convertible Preferred Stock, $0.0001 par value; 11,000 shares authorized, 3,906 shares issued and outstanding at September 30, 2017 and December 31, 2016, and liquidation preference of $3,906 at September 30, 2017 and December 31, 2016 | 3,906 | 3,906 | ||||||
Series F Convertible Preferred Stock, $0.0001 par value; 10,000 shares authorized, 2,737 shares issued and outstanding at September 30, 2017 and December 31, 2016, and liquidation preference of $2,737 at September 30, 2017 and December 31, 2016 | 2,737 | 2,737 | ||||||
Additional paid-in capital | 796,118 | 661,103 | ||||||
Accumulated deficit | (682,968 | ) | (606,711 | ) | ||||
Total shareholders’ equity | 119,795 | 61,037 | ||||||
Total liabilities and shareholders’ equity | $ | 130,057 | $ | 70,795 |
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La Jolla Pharmaceutical Company
Sandra Vedrick
Associate
Director, Investor Relations & Human Resources
(858)
256-7910
[email protected]
or
La
Jolla Pharmaceutical Company
Dennis M. Mulroy
Chief
Financial Officer
(858) 433-6839
[email protected]