BioLineRx (NASDAQ: BLRX) (TASE: BLRX), a clinical-stage
biopharmaceutical company dedicated to identifying, in-licensing and
developing promising therapeutic candidates, today reported its
financial results for the year ended December 31, 2013.
Kinneret Savitsky, Ph.D., CEO of BioLineRx, remarked, “2013 was a
significant year for BioLineRx, with increased efforts in the specific
therapeutic areas of oncology and immunology, as well as an emphasis on
clinical-stage programs. This objective was achieved primarily by
establishing collaboration agreements in the last year for three of our
assets, which has enabled us to focus our resources on our lead
development programs, while still maintaining substantial upside
potential from the partnered programs. As a result of our concentrated
efforts, we succeeded in rapidly advancing our two lead clinical
programs - BL-8040 for the treatment of both acute myeloid leukemia
(AML) and stem cell mobilization, and BL-7010 for the treatment of
celiac disease. We have a strong balance sheet with enough cash to
support our activities over the next three years – thus giving us the
runway necessary to reach significant clinical milestones for our lead
programs.”
Recent Highlights and Achievements
Lead In-House Clinical Development Programs:
BL-8040: Best-in-class CxCR4 antagonist for treating AML and other
hematological indications, including stem cell mobilization:
-
Promising initial Phase 2 results in AML
-
Regulatory submission for stem cell mobilization
-
Orphan disease designation for both AML and stem cell mobilization
-
U.S. patent issued for method of obtaining stem cells
-
U.S. patent granted covering use in immunotherapy
“Over the last year, we made significant progress with BL-8040, our lead
oncology asset. Early results from our Phase 2 study for AML indicate
that BL-8040 is safe at all doses tested to date, and triggers
substantial mobilization of cancer cells from the bone marrow into the
blood stream, thereby increasing their vulnerability to chemotherapy
treatment. In addition, there are initial signs of robust apoptosis of
the cancer cells. We look forward to providing additional information on
the study at the end of the ongoing dose escalation phase, expected
during the second quarter of 2014, with final study results expected
toward the end of 2014/beginning of 2015. Future development plans for
BL-8040 involve additional hematological indications, including
commencement of a clinical study in stem cell mobilization during the
first half of 2014, with final results expected in the second half of
the year,” added Dr. Savitsky.
BL-7010: Novel gliadin binding polymer for celiac disease
-
Initiated blinded Phase 1/2 study in celiac patients
-
Successfully completed dose escalation stage
“Last week, we reported results from the single administration,
dose-escalation stage of our ongoing Phase 1/2 clinical study for our
novel celiac treatment, BL-7010. The escalation stage reached the
highest planned dose without any dose-limiting adverse events, and all
planned doses were found to be safe and well-tolerated. Based on these
positive safety and tolerability results, we plan to proceed with the
repeated administration stage of the study. We expect to report top-line
results and pharmacokinetic (PK) data in mid-2014, and assuming they are
successful, we expect to commence a pivotal efficacy study in celiac
patients by the end of the year. Celiac disease is clearly attracting
increased interest by the pharmaceutical industry over the last year. In
addition, despite the significant need for new treatments, there are
only a handful of clinical-stage projects under development worldwide
for this disease, and we view this as a significant opportunity for our
product.”
Partnered Development Programs:
BL-1040: First-in-class myocardial implant for prevention of
ventricular remodeling following AMI
“BL-1040, being developed by Bellerophon (f/k/a Ikaria) as a
Bioabsorbable Cardiac Matrix (BCM), is in the midst of a pivotal CE Mark
Registration trial. The trial continues to progress at full steam with
more than 75 sites currently active, including approximately 15 in the
U.S., and we are looking forward to the results, which are expected
toward the end of the year.”
Other collaborations
-
Regional collaboration with JHL Biotech for BL-9020, a novel
monoclonal antibody for the treatment of Type 1 diabetes, covering
China and additional Southeast Asia countries
-
Regional co-development deal with CTTQ for BL-8030, for the treatment
of HCV, covering China and Hong Kong
-
Global collaboration agreement for BL-8020, for the treatment of HCV
and other viral indications, covering the transfer of development
rights to Genoscience and Panmed in return for BioLineRx receiving a
percentage of future revenues from the product.
“We successfully entered into three collaboration agreements over the
last year, enabling us to focus our resources on our lead development
programs, while still maintaining substantial upside potential on the
partnered programs. Our collaboration with JHL Biotech also provides us
with a platform for the development and manufacturing of biologics,
which is a capability that we were previously lacking. JHL is a rising
star in the biologics space, backed by a consortium of top-tier venture
capital firms, with an existing world-class facility in Taiwan and the
largest single-use cell culture plant in the world under construction in
China, and we are very excited about this partnership.”
Termination of BL-1020:
“In March 2013, we discontinued the Phase 2/3 CLARITY study of BL-1020,
for the treatment of schizophrenia, following an interim analysis that
indicated the trial would not meet the pre-specified primary efficacy
endpoint. We subsequently performed a complete analysis of the
un-blinded study data on all enrolled patients in order to ascertain
whether there could be potential for the product. No such potential was
determined, and we terminated the program in March 2014.”
Corporate:
-
Appointment of BJ Bormann, Ph.D., to Board of Directors in August 2013
-
Appointment of Sandra Panem, Ph.D., to Board of Directors in February
2014
-
Successful $24.1 million underwritten public offering in March 2014
“We are very excited to welcome Drs. Bormann and Panem to our Board of
Directors. Their combined decades of experience in the healthcare space
will help guide the strategy and development of our pipeline from a
business, scientific and financial perspective. Together with our recent
fundraising, we view both these accomplishments as important steps in
the development and growth of our company, as we continue to strengthen
our presence in the U.S. financial markets and in the global
biopharmaceutical industry. We also look forward with great anticipation
to the several significant catalysts coming up over the next 12 months,”
concluded Dr. Savitsky.
Financial Results for Year Ended December 31, 2013
Research and development expenses for the year ended December 31, 2013
were NIS 44.1 million ($12.7 million), a decrease of NIS 20.2 million
($5.8 million), or 31%, compared to NIS 64.3 million ($18.5 million) for
the year ended December 31, 2012. Without regard to a NIS 6.0 million
one-time reversal of amounts previously accrued to the OCS in respect of
BL-1020, research and development expenses decreased by NIS 14.2 million
($4.1 million). The decrease resulted primarily from lower expenses in
2013 associated with BL-1020, due to termination of the CLARITY clinical
trial in March 2013, which was partially offset by a ramp-up in spending
on other clinical-stage projects introduced during 2011 and 2012.
Sales and marketing expenses for the year ended December 31, 2013 were
NIS 4.1 million ($1.2 million), an increase of NIS 0.9 million ($0.3
million), or 28%, compared to NIS 3.2 million ($0.9 million) for the
year ended December 31, 2012. The increase resulted primarily from
increased business development activities, as well as professional
services incurred in connection with the collaboration agreement signed
with JHL Biotech.
General and administrative expenses for the year ended December 31, 2013
were NIS 13.2 million ($3.8 million), a decrease of NIS 0.8 million
($0.2 million) or 6%, compared to NIS 14.0 million ($4.0 million) for
the year ended December 31, 2012. The small decrease resulted primarily
from one-time expenses for professional services incurred in 2012.
The Company’s operating loss for the year ended December 31, 2013
amounted to NIS 61.4 million ($17.7 million), compared with an operating
loss of NIS 81.6 million ($23.5 million) for the year ended December 31,
2012.
The Company recognized net non-operating income of NIS 4.2 million ($1.2
million) for the year ended December 31, 2013, an increase of NIS 0.2
million ($0.1 million), compared to net non-operating income of NIS 4.0
million ($1.1 million) for the year ended December 31, 2012.
Non-operating income for both periods primarily relates to fair-value
adjustments of liabilities on account of warrants. These fair-value
adjustments were highly influenced by our share price at each period end
(revaluation date).
Net financial expenses amounted to NIS 4.2 million ($1.2 million) for
the year ended December 31, 2013, a change of NIS 5.5 million ($1.6
million), compared to net financial income of NIS 1.3 million ($0.4
million) for the year ended December 31, 2012. Net financial income and
expenses result primarily from changes in the average exchange rate of
the dollar in relation to the NIS during the respective periods, which
have a direct effect on our net assets denominated in dollars.
The Company’s net loss for the year ended December 31, 2013 amounted to
NIS 61.4 million ($17.7 million), compared with a net loss of NIS 76.3
million ($22.0 million) for the year ended December 31, 2012.
The Company held NIS 63.2 million ($18.2 million) in cash, cash
equivalents and short-term bank deposits as of December 31, 2013. In
March 2014, the Company completed an underwritten public offering of its
American Depositary Shares for gross proceeds of $24.1 million.
Net cash used in operating activities was NIS 70.5 million for the year
ended December 31, 2013, compared with NIS 75.1 million for the year
ended December 31, 2012. The NIS 4.6 million ($1.3 million) decrease in
net cash used in operating activities during 2013 resulted primarily
from the decrease in research and development spending.
Net cash used in investing activities for the year ended December 31,
2013 was NIS 19.8 million, compared to net cash provided by investing
activities of NIS 51.3 million for the year ended December 31, 2012. The
changes in cash flows from investing activities relate primarily to
investments in, and maturities of, short-term bank deposits and other
investments during the respective periods.
Net cash provided by financing activities for the year ended December
31, 2013 was NIS 55.2 million, compared to net cash provided by
financing activities of NIS 58.9 million for the year ended December 31,
2012. The cash flows from financing activities in 2013 reflect the
direct placement to OrbiMed completed in February 2013, as well as
funding under the share purchase agreement with Lincoln Park Capital.
The cash flows from financing activities in 2012 reflect the private
placement completed in February 2012.
Conference Call and Webcast Information
BioLineRx will hold a conference call to discuss its year-end 2013
results today, March 17, 2014, at 10:00 a.m. EDT. A presentation will be
available on BioLineRx’s website to accompany management’s remarks on
the call. To access the conference call, please dial 1-888-668-9141 from
the U.S., or +972-3-918-0609 internationally. The call will also be
available via live webcast through BioLineRx’s website. A replay of the
conference call will be available approximately two hours after
completion of the live conference call. To access the replay, please
dial 1-888-269-0005 from the U.S. or +972-3-925-5938 internationally.
The replay will be available through March 20, 2014.
(Tables follow)
About BioLineRx
BioLineRx is a publicly-traded, clinical-stage biopharmaceutical company
dedicated to identifying, in-licensing and developing promising
therapeutic candidates. The Company in-licenses novel compounds
primarily from academic institutions and biotech companies based in
Israel, develops them through pre-clinical and/or clinical stages, and
then partners with pharmaceutical companies for advanced clinical
development and/or commercialization.
BioLineRx’s current portfolio consists of a variety of clinical and
pre-clinical projects, including: BL-1040 for prevention of pathological
cardiac remodeling following a myocardial infarction, which has been
out-licensed to Bellerophon BCM (f/k/a Ikaria) and is in the midst of a
pivotal CE-Mark registration trial; BL-8040 for treating acute myeloid
leukemia (AML) and other hematological indications, which is in the
midst of a Phase 2 study; BL-7010 for celiac disease, which is in the
midst of a Phase 1/2 study; and BL-5010 for non-surgical removal of skin
lesions, which is expected to commence a pivotal CE-mark registration
trial in the first half of 2014.
For more information on BioLineRx, please visit www.biolinerx.com
or download the investor relations mobile device app, which allows users
access to the Company’s SEC documents, press releases, and events.
BioLineRx’s IR app is available on the iTunes App Store as well as the
Google Play Store.
Various statements in this release concerning BioLineRx’s future
expectations constitute “forward-looking statements” within the meaning
of the Private Securities Litigation Reform Act of 1995. These
statements include words such as “may,” “expects,” “anticipates,”
“believes,” and “intends,” and describe opinions about future events.
These forward-looking statements involve known and unknown risks and
uncertainties that may cause the actual results, performance or
achievements of BioLineRx to be materially different from any future
results, performance or achievements expressed or implied by such
forward-looking statements. Some of these risks are: changes in
relationships with collaborators; the impact of competitive products and
technological changes; risks relating to the development of new
products; and the ability to implement technological improvements. These
and other factors are more fully discussed in the “Risk Factors” section
of BioLineRx’s most recent annual report on Form 20-F filed with the
Securities and Exchange Commission on March 17, 2014. In addition, any
forward-looking statements represent BioLineRx’s views only as of the
date of this release and should not be relied upon as representing its
views as of any subsequent date. BioLineRx does not assume any
obligation to update any forward-looking statements unless required by
law.
BioLineRx Ltd.
|
CONSOLIDATED STATEMENTS OF FINANCIAL POSITION
|
|
|
|
|
Convenience translation into USD
|
|
|
|
|
|
December 31,
|
|
|
December 31,
|
|
|
|
|
|
2012
|
|
|
2013
|
|
|
2013
|
|
|
|
|
|
NIS in thousands
|
|
|
In thousands
|
Assets
|
|
|
|
|
|
|
|
|
|
|
|
CURRENT ASSETS
|
|
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents
|
|
|
|
|
68,339
|
|
|
|
30,888
|
|
|
|
8,899
|
|
Short-term bank deposits
|
|
|
|
|
11,459
|
|
|
|
32,345
|
|
|
|
9,319
|
|
Prepaid expenses
|
|
|
|
|
804
|
|
|
|
896
|
|
|
|
258
|
|
Other receivables
|
|
|
|
|
2,254
|
|
|
|
1,249
|
|
|
|
360
|
|
Total current assets
|
|
|
|
|
82,856
|
|
|
|
65,378
|
|
|
|
18,836
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NON-CURRENT ASSETS
|
|
|
|
|
|
|
|
|
|
|
|
Restricted deposits
|
|
|
|
|
3,513
|
|
|
|
573
|
|
|
|
165
|
|
Long-term prepaid expenses
|
|
|
|
|
204
|
|
|
|
169
|
|
|
|
49
|
|
Property and equipment, net
|
|
|
|
|
3,172
|
|
|
|
2,471
|
|
|
|
712
|
|
Intangible assets, net
|
|
|
|
|
1,063
|
|
|
|
878
|
|
|
|
253
|
|
Total non-current assets
|
|
|
|
|
7,952
|
|
|
|
4,091
|
|
|
|
1,179
|
|
Total assets
|
|
|
|
|
90,808
|
|
|
|
69,469
|
|
|
|
20,015
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Liabilities and equity
|
|
|
|
|
|
|
|
|
|
|
|
CURRENT LIABILITIES
|
|
|
|
|
|
|
|
|
|
|
|
Current maturities of long-term bank loan
|
|
|
|
|
137
|
|
|
|
-
|
|
|
|
-
|
|
Accounts payable and accruals:
|
|
|
|
|
|
|
|
|
|
|
|
Trade
|
|
|
|
|
12,283
|
|
|
|
7,945
|
|
|
|
2,289
|
|
OCS
|
|
|
|
|
6,148
|
|
|
|
-
|
|
|
|
-
|
|
Other
|
|
|
|
|
5,443
|
|
|
|
2,499
|
|
|
|
720
|
|
Total current liabilities
|
|
|
|
|
24,011
|
|
|
|
10,444
|
|
|
|
3,009
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NON-CURRENT LIABILITIES
|
|
|
|
|
|
|
|
|
|
|
|
Retirement benefit obligations
|
|
|
|
|
143
|
|
|
|
152
|
|
|
|
44
|
|
Warrants
|
|
|
|
|
10,725
|
|
|
|
18,187
|
|
|
|
5,240
|
|
Total non-current liabilities
|
|
|
|
|
10,868
|
|
|
|
18,339
|
|
|
|
5,284
|
|
COMMITMENTS AND CONTINGENT LIABILITIES
|
|
|
|
|
|
|
|
|
|
|
|
Total liabilities
|
|
|
|
|
34,879
|
|
|
|
28,783
|
|
|
|
8,293
|
|
|
|
|
|
|
|
|
|
|
|
|
|
EQUITY
|
|
|
|
|
|
|
|
|
|
|
|
Ordinary shares
|
|
|
|
|
1,837
|
|
|
|
2,414
|
|
|
|
696
|
|
Share premium
|
|
|
|
|
464,629
|
|
|
|
509,857
|
|
|
|
146,890
|
|
Capital reserve
|
|
|
|
|
33,802
|
|
|
|
34,192
|
|
|
|
9,851
|
|
Accumulated deficit
|
|
|
|
|
(444,339
|
)
|
|
|
(505,777
|
)
|
|
|
(145,715
|
)
|
Total equity
|
|
|
|
|
55,929
|
|
|
|
40,686
|
|
|
|
11,722
|
|
Total liabilities and equity
|
|
|
|
|
90,808
|
|
|
|
69,469
|
|
|
|
20,015
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BioLineRx Ltd.
|
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Year ended December 31,
|
|
|
Convenience translation into USD
|
|
|
|
|
|
2011
|
|
|
2012
|
|
|
2013
|
|
|
2013
|
|
|
|
|
|
NIS in thousands
|
|
|
In thousands
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
RESEARCH AND DEVELOPMENT EXPENSES, NET
|
|
|
|
|
(42,623
|
)
|
|
|
(64,304
|
)
|
|
|
(44,057
|
)
|
|
|
(12,692
|
)
|
SALES AND MARKETING EXPENSES
|
|
|
|
|
(3,308
|
)
|
|
|
(3,227
|
)
|
|
|
(4,101
|
)
|
|
|
(1,182
|
)
|
GENERAL AND ADMINISTRATIVE EXPENSES
|
|
|
|
|
(12,722
|
)
|
|
|
(14,026
|
)
|
|
|
(13,225
|
)
|
|
|
(3,810
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
OPERATING LOSS
|
|
|
|
|
(58,653
|
)
|
|
|
(81,557
|
)
|
|
|
(61,383
|
)
|
|
|
(17,684
|
)
|
NON-OPERATING INCOME, NET
|
|
|
|
|
-
|
|
|
|
3,958
|
|
|
|
4,191
|
|
|
|
1,207
|
|
FINANCIAL INCOME
|
|
|
|
|
12,730
|
|
|
|
8,819
|
|
|
|
2,600
|
|
|
|
749
|
|
FINANCIAL EXPENSES
|
|
|
|
|
(4,263
|
)
|
|
|
(7,490
|
)
|
|
|
(6,846
|
)
|
|
|
(1,972
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NET LOSS AND COMPREHENSIVE LOSS
|
|
|
|
|
(50,186
|
)
|
|
|
(76,270
|
)
|
|
|
(61,438
|
)
|
|
|
(17,700
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
NIS
|
|
|
USD
|
LOSS PER ORDINARY SHARE - BASIC
|
|
|
|
|
(0.41
|
)
|
|
|
(0.45
|
)
|
|
|
(0.27
|
)
|
|
|
(0.08
|
)
|
LOSS PER ORDINARY SHARE - DILUTED
|
|
|
|
|
(0.41
|
)
|
|
|
(0.45
|
)
|
|
|
(0.27
|
)
|
|
|
(0.08
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BioLineRx Ltd.
|
CONSOLIDATED CASH FLOW STATEMENTS
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Year ended December 31,
|
|
|
Convenience translation into USD
|
|
|
|
|
|
2011
|
|
|
2012
|
|
|
2013
|
|
|
2013
|
|
|
|
|
|
NIS in thousands
|
|
|
In thousands
|
CASH FLOWS - OPERATING ACTIVITIES
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss
|
|
|
|
|
(50,186
|
)
|
|
|
(76,270
|
)
|
|
|
(61,438
|
)
|
|
|
(17,700
|
)
|
Adjustments required to reflect net cash used in operating
activities (see appendix below)
|
|
|
|
|
7,445
|
|
|
|
1,125
|
|
|
|
(9,026
|
)
|
|
|
(2,600
|
)
|
Net cash used in operating activities
|
|
|
|
|
(42,711
|
)
|
|
|
(75,145
|
)
|
|
|
(70,464
|
)
|
|
|
(20,300
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
CASH FLOWS - INVESTING ACTIVITIES
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Investments in short-term deposits
|
|
|
|
|
(63,456
|
)
|
|
|
(12,025
|
)
|
|
|
(129,359
|
)
|
|
|
(37,268
|
)
|
Maturities of short-term deposits
|
|
|
|
|
27,308
|
|
|
|
64,801
|
|
|
|
107,049
|
|
|
|
30,841
|
|
Investments in restricted deposits
|
|
|
|
|
(1,000
|
)
|
|
|
(775
|
)
|
|
|
-
|
|
|
|
-
|
|
Maturities of restricted deposits
|
|
|
|
|
675
|
|
|
|
-
|
|
|
|
2,900
|
|
|
|
835
|
|
Purchase of property and equipment
|
|
|
|
|
(951
|
)
|
|
|
(598
|
)
|
|
|
(309
|
)
|
|
|
(89
|
)
|
Purchase of intangible assets
|
|
|
|
|
(133
|
)
|
|
|
(61
|
)
|
|
|
(99
|
)
|
|
|
(29
|
)
|
Net cash provided by (used in) investing activities
|
|
|
|
|
(37,557
|
)
|
|
|
51,342
|
|
|
|
(19,818
|
)
|
|
|
(5,710
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
CASH FLOWS - FINANCING ACTIVITIES
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Issuance of share capital and warrants, net of issuance expenses
|
|
|
|
|
-
|
|
|
|
59,207
|
|
|
|
55,306
|
|
|
|
15,934
|
|
Repayments of bank loan
|
|
|
|
|
(308
|
)
|
|
|
(300
|
)
|
|
|
(127
|
)
|
|
|
(37
|
)
|
Proceeds from exercise of employee stock options
|
|
|
|
|
1
|
|
|
|
2
|
|
|
|
10
|
|
|
|
3
|
|
Net cash provided by (used in) financing activities
|
|
|
|
|
(307
|
)
|
|
|
58,909
|
|
|
|
55,189
|
|
|
|
15,900
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
INCREASE (DECREASE) IN CASH AND CASH EQUIVALENTS
|
|
|
|
|
(80,605
|
)
|
|
|
35,106
|
|
|
|
(35,093
|
)
|
|
|
(10,110
|
)
|
CASH AND CASH EQUIVALENTS - BEGINNING OF YEAR
|
|
|
|
|
111,746
|
|
|
|
33,061
|
|
|
|
68,339
|
|
|
|
19,689
|
|
EXCHANGE DIFFERENCES ON CASH AND CASH EQUIVALENTS
|
|
|
|
|
1,920
|
|
|
|
172
|
|
|
|
(2,358
|
)
|
|
|
(680
|
)
|
CASH AND CASH EQUIVALENTS - END OF YEAR
|
|
|
|
|
33,061
|
|
|
|
68,339
|
|
|
|
30,888
|
|
|
|
8,899
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BioLineRx Ltd.
|
CONSOLIDATED CASH FLOW STATEMENTS (cont.)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Year ended December 31,
|
|
|
Convenience translation into USD
|
|
|
|
|
|
2011
|
|
|
2012
|
|
|
2013
|
|
|
2013
|
|
|
|
|
|
NIS in thousands
|
|
|
In thousands
|
APPENDIX
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Adjustments required to reflect net cash provided by (used in)
operating activities:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Income and expenses not involving cash flows:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Depreciation and amortization
|
|
|
|
|
1,563
|
|
|
|
1,524
|
|
|
|
1,147
|
|
|
|
330
|
|
Impairment of intangible assets
|
|
|
|
|
88
|
|
|
|
-
|
|
|
|
137
|
|
|
|
40
|
|
Retirement benefit obligations
|
|
|
|
|
53
|
|
|
|
60
|
|
|
|
9
|
|
|
|
3
|
|
Long-term prepaid expenses
|
|
|
|
|
(8
|
)
|
|
|
-
|
|
|
|
35
|
|
|
|
10
|
|
Exchange differences on cash and cash equivalents
|
|
|
|
|
(1,920
|
)
|
|
|
(172
|
)
|
|
|
2,358
|
|
|
|
679
|
|
Warrant issuance costs
|
|
|
|
|
-
|
|
|
|
1,204
|
|
|
|
470
|
|
|
|
135
|
|
Gain on adjustment of warrants to fair value
|
|
|
|
|
-
|
|
|
|
(7,265
|
)
|
|
|
(5,169
|
)
|
|
|
(1,489
|
)
|
Commitment fee paid by issuance of share capital
|
|
|
|
|
-
|
|
|
|
880
|
|
|
|
-
|
|
|
|
-
|
|
Share-based compensation
|
|
|
|
|
3,983
|
|
|
|
3,138
|
|
|
|
3,040
|
|
|
|
876
|
|
Interest and exchange differences on short-term deposits
|
|
|
|
|
(1,597
|
)
|
|
|
1,547
|
|
|
|
1,424
|
|
|
|
410
|
|
Interest and linkage differences on bank loan
|
|
|
|
|
(14
|
)
|
|
|
20
|
|
|
|
(10
|
)
|
|
|
(3
|
)
|
Interest and exchange differences on restricted deposits
|
|
|
|
|
(7
|
)
|
|
|
8
|
|
|
|
40
|
|
|
|
12
|
|
|
|
|
|
|
2,141
|
|
|
|
944
|
|
|
|
3,481
|
|
|
|
1,003
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Changes in operating asset and liability items:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Decrease in trade accounts receivable and other receivables
|
|
|
|
|
1,847
|
|
|
|
1,454
|
|
|
|
913
|
|
|
|
263
|
|
Decrease in accounts payable and accruals
|
|
|
|
|
3,457
|
|
|
|
(1,273
|
)
|
|
|
(13,420
|
)
|
|
|
(3,866
|
)
|
|
|
|
|
|
5,304
|
|
|
|
181
|
|
|
|
(12,507
|
)
|
|
|
(3,603
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
7,445
|
|
|
|
1,125
|
|
|
|
(9,026
|
)
|
|
|
(2,600
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Supplementary information on investing and financing activities
not involving cash flows:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Credit received in connection with purchase of property and equipment
|
|
|
|
|
265
|
|
|
|
10
|
|
|
|
-
|
|
|
|
-
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Supplementary information on interest received in cash
|
|
|
|
|
1,825
|
|
|
|
1,720
|
|
|
|
503
|
|
|
|
145
|
|
Copyright Business Wire 2014