[March 14, 2018] |
|
AmpliPhi Biosciences Reports Fourth Quarter and Full Year 2017 Financial Results and Business Highlights
AmpliPhi Biosciences Corporation (NYSE American: APHB), a
clinical-stage biotechnology company focused on precisely targeted
bacteriophage therapeutics for antibiotic-resistant infections, today
announced financial results for the fourth quarter and full year ended
December 31, 2017. AmpliPhi Biosciences will not be conducting a
conference call in conjunction with this financial release.
"I'm delighted to report that AmpliPhi made progress in the fourth
quarter and into 2018," said Paul C. Grint, M.D., CEO of AmpliPhi
Biosciences. "The highlight of the period was the announcement of
positive topline results from our expanded access program to treat
severely ill patients with AB-SA01 or AB-PA01, our bacteriophage
therapeutic candidates targeting resistant Staphylococcus aureus
and Pseudomonas aeruginosa infections. Expansion of this
innovative and potentially life-saving program continues, as evidenced
by the collaboration agreement we recently signed with the U.S.
Department of Veterans Affairs. Our plan remains to bring the data to
the FDA in mid-2018, obtain feedback on the path to regulatory approval,
and potentially initiate a Phase 2 or registrational clinical study as
early as the second half of 2018."
Recent Business Highlights
-
Announced positive topline results for the first seven patients
treated under ongoing single-patient expanded access program. Six of
the seven patients (86%) achieved treatment success (physician's
assessment), defined as complete resolution or significant improvement
of baseline signs and symptoms. All patients were severely ill with
life-threatening infections and unresponsive to antibiotics at the
time of treatment.
-
Provided a corporate update during an investor conference call on
January 3, 2018, outlining the company's 2018 clinical strategy and
the various approaches the company is taking to fund Phase 2 clinical
development of its bacteriophage therapeutics.
-
Completed a public offering of 4,000,000 shares of common stock in
January 2018, at a price to the public of $1.00 per share, for gross
proceeds of $4.0 million.
-
Signed a Cooperative Research and Development Agreement (CRADA) with
the U.S. Department of Veterans Affairs covering expanded access
treatment for AB-SA01 and AB-PA01. Mark Holodniy, M.D., Professor of
Medicine (infectious diseases) at Stanford University and the Veterans
Affairs Palo Alto (News - Alert) Health Care System and Director of the Public Health
Surveillance for the Department of Veterans Affairs, will be the
Principal Investigator leading the collaboration.
Fourth Quarter 2017 Financial Results
-
Research and development (R&D) expenses for the fourth quarter of 2017
were $1.1 million compared to $0.8 million for the fourth quarter of
2016.
-
General and administrative (G&A) expenses were $1.3 million for the
fourth quarter of 2017 compared to $1.5 million for the fourth quarter
of 2016. The decrease was primarily due to a decrease in non-cash
stock-based compensation.
Full-Year 2017 Financial Results
-
R&D expenses for 2017 were $2.9 million compared to $5.7 million for
2016. The decrease was due to lower professional and consulting fees
and clinical expenses. R&D expenses were offset by $2.0 million in tax
rebates from the Australian government for qualified R&D expenditures
in 2017 compared to $0.9 million in 2016.
-
G&A expenses for 2017 were $7.6 million compared to $8.4 million in
2016. The decrease was primarily attributable to decreases in non-cash
stock-based compensation and other charges in 2017.
-
Net cash used in operating activities for 2017 was $9.2 million
compared to $10.6 million for 2016.
-
Cash and cash equivalents as of December 31, 2017 totaled $5.1 million.
-
As of March 14, 2018, there were 13.7 million shares of common stock
outstanding.
-
The audit opinion included in the company's Annual Report on Form 10-K
for the year ended December 31, 2017 contains a going concern
explanatory paragraph. The company is exploring multiple financing
options.
About AmpliPhi Biosciences
AmpliPhi Biosciences Corporation is a clinical-stage biotechnology
company focused on the development of precisely targeted bacteriophage
therapeutics for patients with serious and life-threatening
antibiotic-resistant bacterial infections. AmpliPhi's lead product
candidates, AB-SA01 and AB-PA01, target multidrug-resistant Staphylococcus
aureus and Pseudomonas aeruginosa, which are included on
the WHO's 2017 Priority Pathogens List. Phage therapeutics are uniquely
positioned to address the threat of antibiotic resistance as they can be
precisely targeted to kill select bacteria, have a differentiated
mechanism of action, can penetrate and disrupt biofilms (a common
bacterial defense mechanism against antibiotics), are potentially
synergistic with antibiotics and have been shown to restore antibiotic
sensitivity to drug-resistant bacteria.
Forward-Looking Statements
Statements in this press release that are not statements of historical
fact are forward-looking statements within the meaning of the Private
Securities Litigation Reform Act of 1995. Such forward-looking
statements include, without limitation, statements regarding: AmpliPhi's
plan to present data from expanded access clinical cases to the FDA in
mid-2018, obtain feedback on the path to regulatory approval, and
potentially initiate a Phase 2 or registrational clinical study as early
as the second half of 2018; and the potential benefits of phage therapy
and the potential use of bacteriophages to treat bacterial infections,
including infections that do not respond to antibiotics or are
associated with biofilms. Words such as "believe," "anticipate," "plan,"
"expect," "intend," "will," "may," "goal," "potential" and similar
expressions are intended to identify forward-looking statements, though
not all forward-looking statements necessarily contain these identifying
words. Among the factors that could cause actual results to differ
materially from those indicated in these forward-looking statements are
risks and uncertainties associated with bacteriophage product candidate
development, both generally and specifically through expanded access
regulations, AmpliPhi's financial condition, and other risks and
uncertainties described in AmpliPhi's Annual Report on Form 10-K for the
year ended December 31, 2016, as filed with the Securities and Exchange
Commission (SEC (News - Alert)), and AmpliPhi's subsequent filings with the SEC. You
are cautioned not to place undue reliance on these forward-looking
statements, which speak only as of the date of this press release. All
forward-looking statements are qualified in their entirety by this
cautionary statement, and AmpliPhi undertakes no obligation to revise or
update any forward-looking statements to reflect events or circumstances
after the date of this press release.
AmpliPhi Biosciences Corporation
|
Condensed Consolidated Balance Sheets
|
|
|
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December 31,
|
|
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2017
|
|
2016
|
|
|
|
|
|
Assets
|
|
|
|
|
Cash and cash equivalents
|
|
$
|
5,132,000
|
|
$
|
5,711,000
|
Prepaids and other current assets
|
|
|
253,000
|
|
|
602,000
|
Total current assets
|
|
|
5,385,000
|
|
|
6,313,000
|
Property and equipment, net
|
|
|
816,000
|
|
|
1,072,000
|
Intangible assets, net
|
|
|
4,937,000
|
|
|
10,768,000
|
Total assets
|
|
$
|
11,138,000
|
|
$
|
18,153,000
|
|
|
|
|
|
Liabilities and stockholders' equity
|
|
|
|
|
Total current liabilities
|
|
$
|
1,968,000
|
|
$
|
3,538,000
|
Derivative liabilities
|
|
|
292,000
|
|
|
2,443,000
|
Deferred tax liability
|
|
|
1,147,000
|
|
|
2,449,000
|
Total liabilities
|
|
|
3,407,000
|
|
|
8,430,000
|
|
|
|
|
|
|
|
|
|
|
Stockholders' equity
|
|
|
7,731,000
|
|
|
9,723,000
|
Total liabilities and stockholders' equity
|
|
$
|
11,138,000
|
|
$
|
18,153,000
|
|
AmpliPhi Biosciences Corporation
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Condensed Consolidated Statements of Operations
|
|
|
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Three Months Ended December 31,
|
|
Year Ended December 31,
|
|
|
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2017
|
|
|
|
2016
|
|
|
|
2017
|
|
|
|
2016
|
|
|
|
(Unaudited)
|
|
(Unaudited)
|
|
|
|
|
Revenue
|
|
$
|
20,000
|
|
|
$
|
22,000
|
|
|
$
|
115,000
|
|
|
$
|
260,000
|
|
Operating expenses:
|
|
|
|
|
|
|
|
|
Research and development
|
|
|
1,090,000
|
|
|
|
802,000
|
|
|
|
2,881,000
|
|
|
|
5,678,000
|
|
General and administrative
|
|
|
1,295,000
|
|
|
|
1,537,000
|
|
|
|
7,590,000
|
|
|
|
8,413,000
|
|
Impairment charges
|
|
|
-
|
|
|
|
9,547,000
|
|
|
|
5,800,000
|
|
|
|
9,547,000
|
|
Total operating expenses
|
|
|
2,385,000
|
|
|
|
11,886,000
|
|
|
|
16,271,000
|
|
|
|
23,638,000
|
|
Loss from operations
|
|
|
(2,365,000
|
)
|
|
|
(11,864,000
|
)
|
|
|
(16,156,000
|
)
|
|
|
(23,378,000
|
)
|
Other income (expense):
|
|
|
|
|
|
|
|
|
Change in fair value of derivative liabilities
|
|
|
13,000
|
|
|
|
1,791,000
|
|
|
|
2,010,000
|
|
|
|
4,538,000
|
|
Other income (expense), net
|
|
|
-
|
|
|
|
17,000
|
|
|
|
6,000
|
|
|
|
(554,000
|
)
|
Total other income, net
|
|
|
13,000
|
|
|
|
1,808,000
|
|
|
|
2,016,000
|
|
|
|
3,984,000
|
|
Loss before income taxes
|
|
|
(2,352,000
|
)
|
|
|
(10,056,000
|
)
|
|
|
(14,140,000
|
)
|
|
|
(19,394,000
|
)
|
Income tax benefit
|
|
|
-
|
|
|
|
556,000
|
|
|
|
1,302,000
|
|
|
|
556,000
|
|
Net loss
|
|
|
(2,352,000
|
)
|
|
|
(9,500,000
|
)
|
|
|
(12,838,000
|
)
|
|
|
(18,838,000
|
)
|
Excess of fair value of consideration transferred on conversion of
Series B preferred stock
|
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
|
(3,580,000
|
)
|
Accretion of Series B preferred stock
|
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
|
(1,858,000
|
)
|
Net loss attributable to common stockholders
|
|
$
|
(2,352,000
|
)
|
|
$
|
(9,500,000
|
)
|
|
$
|
(12,838,000
|
)
|
|
$
|
(24,276,000
|
)
|
Net loss per share of common stock - basic
|
|
$
|
(0.25
|
)
|
|
$
|
(7.02
|
)
|
|
$
|
(2.01
|
)
|
|
$
|
(24.67
|
)
|
Weighted average number of shares of common stock outstanding - basic
|
|
|
9,493,140
|
|
|
|
1,353,767
|
|
|
|
6,387,425
|
|
|
|
983,846
|
|
Net loss per share of common stock - diluted
|
|
$
|
(0.25
|
)
|
|
$
|
(7.57
|
)
|
|
$
|
(2.18
|
)
|
|
$
|
(24.67
|
)
|
Weighted average number of shares of common stock outstanding -
diluted
|
|
|
9,493,140
|
|
|
|
1,405,608
|
|
|
|
6,574,117
|
|
|
|
983,846
|
|
|
AmpliPhi Biosciences Corporation
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Condensed Consolidated Statement of Cash Flows
|
|
|
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Year Ended December 31,
|
|
|
|
2017
|
|
|
|
2016
|
|
|
|
|
|
|
Operating activities:
|
|
|
|
|
Net loss
|
|
$
|
(12,838,000
|
)
|
|
$
|
(18,838,000
|
)
|
Adjustments required to reconcile net loss to net cash used in
operating activities:
|
|
|
|
|
Change in fair value of derivative liabilities
|
|
|
(2,010,000
|
)
|
|
|
(4,538,000
|
)
|
Impairment charges
|
|
|
5,800,000
|
|
|
|
9,547,000
|
|
Stock-based compensation
|
|
|
700,000
|
|
|
|
1,995,000
|
|
Deferred taxes
|
|
|
(1,302,000
|
)
|
|
|
(556,000
|
)
|
Charge for common stock issuance
|
|
|
519,000
|
|
|
|
-
|
|
Costs related to equity offerings
|
|
|
-
|
|
|
|
569,000
|
|
Warrants and other non-cash adjustments, net
|
|
|
22,000
|
|
|
|
193,000
|
|
Depreciation and amortization
|
|
|
374,000
|
|
|
|
369,000
|
|
Changes in operating assets and liabilities, net
|
|
|
(457,000
|
)
|
|
|
653,000
|
|
Net cash used in operating activities
|
|
|
(9,192,000
|
)
|
|
|
(10,606,000
|
)
|
Investing activities:
|
|
|
|
|
Purchases of property and equipment
|
|
|
(58,000
|
)
|
|
|
(279,000
|
)
|
Net cash used in investing activities
|
|
|
(58,000
|
)
|
|
|
(279,000
|
)
|
Financing activities:
|
|
|
|
|
Proceeds from sale of common stock and related warrants, net of
offering costs
|
|
|
9,353,000
|
|
|
|
7,566,000
|
|
Other financing activities, net
|
|
|
(682,000
|
)
|
|
|
(340,000
|
)
|
Net cash provided by financing activities
|
|
|
8,671,000
|
|
|
|
7,226,000
|
|
Net decrease in cash and cash equivalents
|
|
|
(579,000
|
)
|
|
|
(3,659,000
|
)
|
Cash and cash equivalents, beginning of period
|
|
|
5,711,000
|
|
|
|
9,370,000
|
|
Cash and cash equivalents, end of period
|
|
$
|
5,132,000
|
|
|
$
|
5,711,000
|
|
View source version on businesswire.com: http://www.businesswire.com/news/home/20180314005874/en/
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