IRVINE, Calif., Aug. 9, 2017 /PRNewswire/ -- Novus Therapeutics, Inc. (NASDAQ: NVUS), a development stage specialty pharmaceutical company focused on the development of products for disorders of the ear, nose, and throat (ENT), today reported results for the second quarter 2017.
For the three months ended June 30, 2017, the Novus reported a net loss of $6.7 million or $1.32 per share. This compares to a net loss of $1.0 million or $2.25 per share for the same period in the prior year. For the six months ended June 30, 2017, Novus reported a net loss of $8.0 million or $2.51 per share. This compares to a net loss of $2.1 million or $4.68 per share for the same period in the prior year. Novus ended the second quarter of 2017 with $22.5 million in cash and cash equivalents.
"The second quarter was a transformational period for the company," said Gregory J. Flesher, President and Chief Executive Officer. "We completed the previously announced merger with Tokai Pharmaceuticals, Inc., made changes to the leadership team, consolidated operations to our Irvine headquarters, and embarked on a focused effort to advance OP-02 as a potential first-in-class treatment option for the millions of patients burdened by otitis media."
Recent Business Highlights and Corporate Update
- Completion of the Merger: On May 9, 2017, the previously announced merger between Otic Pharma, Ltd. and Tokai Pharmaceuticals, Inc. was completed and the name of the combined company was changed to Novus Therapeutics, Inc. On May 11, 2017, Novus began trading on the NASDAQ Capital Market under the ticker symbol "NVUS."
- Financing Activities: Novus raised an additional $7.1 million in gross proceeds in connection with the merger. The proceeds included $4.0 million obtained through a private placement of the company's common stock on May 10, 2017 and approximately $3.1 million obtained through the exercise of Otic Pharma, Ltd. warrants prior to close of the merger.
- Leadership Change: Jon Kuwahara joined Novus as Senior Vice President of Finance and Administration, succeeding Christine Ocampo. Mr. Kuwahara has over 25 years of finance and operations experience, primarily within the pharmaceutical industry. Mr. Kuwahara is a member of the Board of Directors, and Chairman of the Audit Committee, for Emmaus Life Sciences, Inc. and has held past finance roles at Espero Pharmaceuticals, Avanir Pharmaceuticals, and Questcor Pharmaceuticals.
- Research and Development: Given the current capital resources, Novus made the strategic decision to focus substantially all of its development activities to the advancement of OP-02 for otitis media, an opportunity management believes has the greatest potential to create significant shareholder value. Novus is currently conducting formulation development activities on OP-02, and upon successful completion and manufacturing of clinical supply, plans to begin human studies in 2018. Novus currently maintains nine prostate cancer patients in a safety study of galeterone, but has terminated all other research and development activities related to galeterone.
Financial Results for the Three Months and Six Months Ended June 30, 2017
Research and development expenses for the three-month and six-month periods ended June 30, 2017 decreased to approximately $0.5 million and $1.0 million, as compared to $0.6 million and $1.3 million respectively, for the same periods in 2016. The change was primarily attributed to decreased spending towards OP-01 and offset by costs incurred for Tokai's legacy development programs during 2017.
General and administrative expenses for the three-month and six-month periods ended June 30, 2017 increased to approximately $6.1 million and $7.0 million, as compared to $0.3 million and $0.8 million, respectively for the same periods in 2016. The change was primarily attributed to $5.4 million in one-time merger related expenses for the three-month period ended June 30, 2017 and public company related expenses, including severance costs for previous Tokai employees.
About Novus Therapeutics
Novus Therapeutics is a development stage pharmaceutical company focused on the development of products for disorders of the ear, nose, and throat (ENT). Novus has two technologies, each of which has the potential to be developed for multiple ENT indications. The company's lead product (OP-02) is a surfactant-based, combination drug product being developed as a potential first-in-class treatment option for patients at risk for or with otitis media ("OM") (middle ear inflammation with or without infection), which is often caused by Eustachian tube dysfunction ("ETD"). Globally, OM affects more than 700 million adults and children every year. OM is a common disorder seen in pediatric practice, and in the United States is the most frequent reason children are prescribed antibiotics and undergo surgery. Novus also has a foam-based drug delivery technology (OP-01), which may be developed in the future for delivery of drugs into the ear, nose, and sinus cavities. For more information on Novus, please visit novustherapeutics.com.
Forward-looking Statements
Any statements in this press release about the company's future expectations, plans and prospects, including statements about its strategy, future operations, development of its product candidates, the review of strategic alternatives and the outcome of such review and other statements containing the words "believes," "anticipates," "plans," "expects," "may," and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Forward-looking statements include, but are not limited to, expectations regarding the timing for the commencement and completion of our clinical trials and our ability to accelerate the development of our drug candidates. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including: the sufficiency of the company's cash resources; the ability to timely develop and manufacture clinical batches of our study drugs; the ability to obtain necessary approvals to commence additional clinical trials; whether data from early clinical trials will be indicative of the data that will be obtained from future clinical trials; whether the results of clinical trials will warrant submission for regulatory approval of any investigational product, any such submission will receive approval from the United States Food and Drug Administration or equivalent foreign regulatory agencies and, if we are able to obtain such approval for an investigational product, it will be successfully distributed and marketed. Any forward-looking statements contained in this press release speak only as of the date hereof and not of any future date, and the company expressly disclaims any intent to update any forward-looking statements, whether as a result of new information, future events or otherwise.
Investor Contacts
The Trout Group
Gita Ogawa
Tel: (646) 378-2949
[email protected]
Novus Therapeutics, Inc.
Investor Relations
Tel: (949) 238-8090
[email protected]
NOVUS THERAPEUTICS, INC. |
||||||||
CONDENSED CONSOLIDATED BALANCE SHEETS |
||||||||
(In thousands, except share and per share data) |
||||||||
June 30, |
December 31, |
|||||||
ASSETS |
||||||||
Current assets: |
||||||||
Cash and cash equivalents |
$ |
22,498 |
$ |
1,103 |
||||
Restricted cash |
13 |
14 |
||||||
Prepaid expenses and other current assets |
2,332 |
33 |
||||||
Total current assets |
24,843 |
1,150 |
||||||
Property and equipment, net |
49 |
31 |
||||||
Restricted cash |
70 |
— |
||||||
Goodwill |
1,867 |
— |
||||||
Other assets |
15 |
15 |
||||||
Total assets |
$ |
26,844 |
$ |
1,196 |
||||
LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT) |
||||||||
Current liabilities: |
||||||||
Accounts payable |
$ |
374 |
$ |
338 |
||||
Accrued severance |
1,300 |
— |
||||||
Accrued expenses and other liabilities |
1,486 |
113 |
||||||
Convertible notes |
— |
3,447 |
||||||
Total current liabilities |
3,160 |
3,898 |
||||||
Long-term liabilities |
245 |
— |
||||||
Total liabilities |
3,405 |
3,898 |
||||||
Commitments and contingencies |
||||||||
Stockholders' equity (deficit): |
||||||||
Preferred stock, $0.001 par value, 5,000,000 shares authorized; 0 and 452,706 shares issued and outstanding at June 30, 2017 and December 31, 2016 |
— |
11 |
||||||
Common stock, $0.001 par value, 200,000,000 shares authorized; 6,943,832 and 82,246 shares issued and outstanding at June 30, 2017 and December 31, 2016, respectively |
7 |
1 |
||||||
Additional paid-in capital |
45,858 |
11,385 |
||||||
Goodwill |
— |
291 |
||||||
Accumulated deficit |
(22,426) |
(14,390) |
||||||
Total stockholders' equity (deficit) |
23,439 |
(2,702) |
||||||
Total liabilities and stockholders' equity (deficit) |
$ |
26,844 |
$ |
1,196 |
NOVUS THERAPEUTICS, INC. |
||||||||||||||||
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS |
||||||||||||||||
(Unaudited) |
||||||||||||||||
(In thousands, except share and per share data) |
||||||||||||||||
Three Months Ended |
Six Months Ended |
|||||||||||||||
2017 |
2016 |
2017 |
2016 |
|||||||||||||
Operating expenses |
||||||||||||||||
Research and development |
$ |
533 |
$ |
592 |
$ |
1,012 |
$ |
1,282 |
||||||||
General and administrative |
6,133 |
340 |
7,039 |
762 |
||||||||||||
Total operating expenses |
6,666 |
932 |
8,051 |
2,044 |
||||||||||||
Loss from operations |
(6,666) |
(932) |
(8,051) |
(2,044) |
||||||||||||
Other income (loss), net |
4 |
(70) |
15 |
(61) |
||||||||||||
Net loss and comprehensive loss |
$ |
(6,662) |
$ |
(1,002) |
$ |
(8,036) |
$ |
(2,105) |
||||||||
Net loss per share, basic and diluted |
$ |
(1.32) |
$ |
(2.25) |
$ |
(2.51) |
$ |
(4.68) |
||||||||
Weighted-average shares outstanding, basic and diluted |
4,154,842 |
77,856 |
2,270,907 |
77,856 |
NOVUS THERAPEUTICS, INC. |
||||||||
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS |
||||||||
(Unaudited) |
||||||||
(In thousands) |
||||||||
Six Months Ended |
||||||||
2017 |
2016 |
|||||||
Operating activities |
||||||||
Net loss |
$ |
(8,036) |
$ |
(2,105) |
||||
Adjustments to reconcile net loss to net cash used in operating activities: |
||||||||
Depreciation and amortization |
16 |
20 |
||||||
Stock-based compensation |
236 |
85 |
||||||
Loss on disposal of fixed assets |
31 |
— |
||||||
Changes in operating assets and liabilities: |
||||||||
Prepaid expenses and other assets |
(1,167) |
45 |
||||||
Accounts payable and accrued expenses |
7 |
(207) |
||||||
Net cash used in operating activities |
(8,913) |
(2,162) |
||||||
Investing activities |
||||||||
Cash received from merger transaction |
23,250 |
— |
||||||
Proceeds from sale of equipment |
8 |
— |
||||||
Purchase of property and equipment |
— |
(10) |
||||||
Net cash provided by (used in) investing activities |
23,258 |
(10) |
||||||
Financing activities |
||||||||
Proceeds from issuance of common stock, net |
4,000 |
— |
||||||
Proceeds from exercise of warrants |
3,119 |
— |
||||||
Net cash provided by financing activities |
7,119 |
— |
||||||
Net increase (decrease) in cash, cash equivalents and restricted cash |
21,464 |
(2,172) |
||||||
Cash, cash equivalents and restricted cash at beginning of period |
1,117 |
3,109 |
||||||
Cash, cash equivalents and restricted cash at end of period |
$ |
22,581 |
$ |
937 |
||||
Supplemental disclosure of cash flow information |
||||||||
Noncash activities: |
||||||||
Conversion of promissory notes and interest to common stock |
$ |
3,447 |
$ |
— |
||||
Conversion of preferred stock to common stock |
$ |
9 |
$ |
— |
||||
Conversion of contingently issuable shares to common stock |
$ |
291 |
$ |
— |
||||
Fair value of assets acquired and liabilities assumed in the merger: |
||||||||
Fair value of assets acquired, excluding cash and restricted cash |
$ |
3,072 |
||||||
Fair value of liabilities assumed |
(2,947) |
|||||||
Fair value of net assets acquired in the merger |
$ |
125 |
SOURCE Novus Therapeutics, Inc.
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