LEIDEN, The Netherlands,
April 30, 2015 /PRNewswire/ --
Biotech company Pharming Group N.V. ("Pharming" or "the
Company") (Euronext Amsterdam: PHARM) today published its
(unaudited) financial report for Q1 2015 ended 31 March 2015.
FINANCIAL HIGHLIGHTS
- Revenues from operations increased to €1.8 million (Q1 2014:
€1.4 million) as a result of increased product sales of €1.2
million (Q1 2014: €0.9 million). Ruconest® sales in the US amounted
to €0.6 million and sales by Sobi in the EU amounted to €0.4
million. Alongside Pharming realised initial direct sales in
Austria, Germany and the
Netherlands. Product sales in the first quarter of 2014 were
a result of Sobi sales for the EU only.
- Gross profit increased to €0.8 million from €0.2 million in Q1
2014 as a result of sales in the US and the absence of additional
impairments on inventory, reflecting the improving yields from
sales in the US and direct commercialization in the EU.
- Operating result in the first quarter 2015 was in line with the
previous year; a loss of €3.0 million .
- Financial income and expenses improved by €14.7 million in the
first quarter to a gain of €1.7 million from a €13.0 million loss
in Q1 2014. The loss in 2014 was a result of a (non-cash)
revaluation of warrants caused by the strong increase of Pharming's
share price during Q1 2014. In Q1 2015 the revaluation of warrants
led to a positive result caused by an decrease of the share
price.
- Net loss of the first quarter 2015 amounted to €1.3 million (Q1
2014: €16.0 million).
- The equity position slightly decreased to €29.3 million
compared to 31 December 2014 as a
result of the net loss in Q1 2015.
- The inventories of Ruconest increased to €14.9 million from
€13.4 million as per 31 December 2014
in preparation of expected sales.
- The cash position decreased during Q1 2015 by €4.1 million to
€30.3 million due to still negative cash flows from operating
activities.
OPERATIONAL HIGHLIGHTS
- Following the completed acquisition of our US partner, Salix,
by Valeant Pharmaceuticals (VRX), the Ruconest US commercial
infrastructure remains intact and commercialisation efforts remain
unaffected
- A steady inflow of new patients into Ruconest Solutions (the US
total care program under which Ruconest is made available to HAE
patients in the US) continued during the quarter, creating the
basis for continued revenue growth from sales in the US
- Patient enrollment for the randomised double blind placebo
controlled Phase II clinical trial to investigate Ruconest for the
prophylaxis of HAE was initiated in January and continued during
the quarter
- In February, Dr. Perry Calias
was appointed as Chief Scientific Officer. Dr. Calias will
have overall responsibility for the Company's new Enzyme
Replacement Therapy (ERT) programs, achieving the scientific
milestones set in the business plan, enhancing the IP portfolio,
overseeing new product development and contributing to the overall
strategic direction of the Company.
Sijmen de Vries, Pharming's CEO, commented: "Pharming's
performance during the first quarter of 2015 has started to reflect
some of the transformational changes made in 2014. In particular,
we have seen the beginning of increasing and profitable Ruconest
sales in the US following the product launch in November. Also as
result of these US sales and the first sales from the direct
commercialisation of Ruconest in the EU, no additional impairments
of inventories were incurred this quarter. We therefore expect
revenues and gross profits to improve due to markedly improved
sales during the remainder of the year.
FINANCIAL RESULTS
Revenues
Revenues increased to €1.8 million (Q1 2014: €1.4 million),
mainly as a result of product sales in the US.
Other license fee income amounted to €0.6 million (Q1 2014: €0.6
million). This license fee income reflects the release of accrued
deferred license fees following receipt of €21.0 million
upfront and milestone payments in 2010 and 2013 from Sobi, Salix
and SIPI.
Cost of product sales in the first quarter of 2015 amounted to
€1.0 million (Q1 2015: €0.9 million). In the first quarter of 2015
the Company incurred no additional inventory impairments (Q1 2014:
€0.4 million), related to cost of goods exceeding the anticipated
sales revenue for the product.
Gross profit
Gross profit increased by €0.6 million, from €0.2 million in the
first quarter of 2014 to €0.8 million in the first quarter of 2015,
mainly as a result of an improving "product mix", from sales in the
US by our partner Salix, direct commercialisation by Pharming in
Austria, Germany and Netherlands and no additional impairments of
inventories.
Operating costs
Operating costs increased to €3.8 million from €3.3 million in
the first quarter of 2014. The increase is a result of the
increased (non-cash) share-based compensation, marketing &
sales expenses for direct commercialization activities in the EU
and costs for the new R&D sites in Schaijk and in France.
Research and Development costs remained unchanged compared to Q1
2014 and amounted to €2.7 million in the first quarter of 2015,
General and Administrative costs increased to €0.9 million from
€0.6 million in 2014 and Marketing and Sales costs amounted to €0.2
million. In 2014 no direct commercialisation of Ruconest took
place.
Operating result
As a result of the increase in gross profit which equaled the
increase of operating costs, the operating loss of
€3.0 million was in line with the first quarter of the
previous year.
Financial income and expenses
The 2015 net gain on financial income and expenses was €1.7
million, compared to a €13.0 million net loss on financial income
and expenses in the first quarter of 2014. The financial income and
expenses reflected the (non-cash) revaluation of warrants and
exchange rate effects on foreign currencies.
Net result
As a result of the above items, the net loss decreased by €14.7
million to €1.3 million in the first quarter of 2015 (Q1 2014:
€16.0 million). The net loss per share for the first quarter of
2015 decreased to €0.003 (Q1 2014: €0.044).
FINANCIAL POSITION
Total cash and cash equivalents (including restricted cash)
decreased by €4.1 million from €34.4 million at the end of 2014 to
€30.3 million at the end of the first quarter 2015. The decrease
follows from net cash outflows from operations of €4.0 million and
investing activities of €0.1 million with net cash outflows from
financing activities amounting to €0.4 million and positive
exchange rate effects amounting to €0.5 million.
EQUITY POSITION
The Company's equity position amounted to €29.3 million at the
end of the first quarter 2015 (31 December
2014: €29.8 million). In addition, it should be noted that
the Company has a significant amount of deferred license fee income
(Q1 2015: €11.7 million) regarding non-refundable license fees
received in 2010 and 2013 which will be recognised in the statement
of income over the term of the license agreements involved.
The number of outstanding shares as of 31
March 2015 is 408.1 million and the fully diluted number of
shares is 477.2 million.
OUTLOOK
For 2015, the Company expects:
- Increasing sales of Ruconest from US partner Salix (Valeant),
EU partner Sobi, Israel partner
Megapharm and the direct commercialisation of Ruconest in
Austria, Germany and the
Netherlands.
- Continued significant investments in purification of sufficient
quantities of Ruconest.
- Investments in the continuing Phase II clinical trial for
Prophylaxis of HAE; a 50/50 cost sharing project with US partner
Salix (Valeant).
- Investments in (early) development of new pipeline projects
driven by the French Research Group and the Boston-based New Product Development
group.
No financial guidance for 2015 is provided.
About Pharming Group N.V.
Pharming Group N.V. is developing innovative products for the
treatment of unmet medical needs. Ruconest® (conestat alfa) is a
recombinant human C1 esterase inhibitor approved for the treatment
of angioedema attacks in patients with HAE in the US, Israel, all 28 EU countries plus Norway, Iceland and Liechtenstein.
Ruconest is commercialised by Pharming in Austria, Germany and the
Netherlands.
Ruconest is distributed by Swedish Orphan Biovitrum AB (publ)
(SS: SOBI) in the other EU countries and in Azerbaijan, Belarus, Georgia, Iceland, Kazakhstan, Liechtenstein, Norway, Russia, Serbia and Ukraine.
Ruconest is partnered with Salix Pharmaceuticals, Ltd. ("Salix")
in North America. Valeant
Pharmaceuticals International, Inc. (NYSE: VRX/TSX: VRX) completed
its acquisition of Salix Pharmaceuticals, Ltd. on April 1, 2015.
Ruconest is also being investigated in a randomised Phase II
clinical trial for prophylaxis of HAE and evaluated for various
additional follow-on indications. Pharming has a unique GMP
compliant, validated platform for the production of recombinant
human proteins that has proven capable of producing industrial
volumes of high quality recombinant human protein in a more
economical way compared to current cell-based technologies. Leads
for Enzyme Replacement Therapy (ERT) in Pompe, Fabry's and
Gaucher's diseases are under early evaluation. The platform is
partnered with Shanghai Institute of Pharmaceutical Industry
(SIPI), a Sinopharm Company, for joint global development of new
products. Pre-clinical development and manufacturing will take
place at SIPI and are funded by SIPI. Pharming and SIPI initially
plan to utilise this platform for the development of recombinant
human Factor VIII for the treatment of Haemophilia A.
Additional information is available on the Pharming website:
http://www.pharming.com.
Forward-looking statements
This press release may contain forward-looking statements
including without limitation those regarding Pharming's (the
"Company") financial projections, market expectations,
developments, partnerships, plans, strategies and capital
expenditures.
The Company cautions that such forward-looking statements may
involve certain risks and uncertainties, and actual results may
differ. Risks and uncertainties include without limitation the
effect of competitive, political and (macro) economic factors,
legal claims, the Company's ability to protect intellectual
property, fluctuations in exchange and interest rates, changes in
tax rates, changes in legislation and the Company's ability to
identify, develop and successfully commercialise new products,
markets or technologies.
As a result, the Company's actual performance, position and
financial results may differ materially from the plans, goals and
expectations set forth in such forward-looking statements. The
Company assumes no obligation to update any
forward-looking statements or information, which speak as of their
respective dates, unless required by law or
regulations.
PHARMING GROUP N.V.
CONDENSED CONSOLIDATED INTERIM FINANCIAL STATEMENTS
(UNAUDITED)
FOR THE FIRST QUARTER ENDED 31 MARCH
2015
Consolidated Statement of Income
Consolidated Statement of Comprehensive Income
Consolidated Balance Sheet
Consolidated Statement of Cash Flows
CONSOLIDATED STATEMENT OF INCOME
For the first quarter ended 31 March
Q1 Q1
Amounts in EUR'000, except per share data 2015 2014
License fees 550 550
Product sales 1,230 869
Revenues 1,780 1,419
Costs of product sales (1,002) (866)
Inventory impairments - (351)
Costs of sales (1,002) (1,217)
Gross profit 778 202
Other income - 33
Research and development (2,712) (2,686)
General and administrative (880) (606)
Marketing and sales (232) -
Costs (3,824) (3,292)
Operating result (3,046) (3,057)
Financial income and expenses 1,718 (12,977)
Result before income tax (1,328) (16,034)
Income tax expense - -
Net result for the year from continuing
operations (1,328) (16,034)
Net result for the year from discontinued
operations - -
Net result for the year (1,328) (16,034)
Attributable to:
Owners of the parent (1,328) (16,034)
Non-controlling interests - -
Total net result (1,328) (16,034)
Basic earnings per share (EUR) from
continuing operations (0,003) (0,044)
CONSOLIDATED STATEMENT OF COMPREHENSIVE INCOME
For the first quarter ended 31 March
Q1 Q1
Amounts in EUR'000 2015 2014
Net result for the year (1,328) (16,034)
Currency translation differences 6 -
Items that may be subsequently reclassified to
profit or loss - -
Other comprehensive income, net of tax - -
Total comprehensive income for the year (1,322) (16,034)
Attributable to:
Owners of the parent
(1,322) (16,034)
Non-controlling interests
- -
CONSOLIDATED BALANCE SHEET
As at 31 March
31 March 31 December
Amounts in EUR'000
2015 2014
Intangible assets 764 777
Property, plant and equipment 5,389 5,598
Restricted cash 200 200
Non-current assets 6,353 6,575
Inventories 14,898 13,404
Trade and other receivables 2,374 1,554
Restricted cash - -
Cash and cash equivalents 30,125 34,185
Current assets 47,397 49,143
Total assets 53,750 55,718
Share capital 4,081 4,077
Share premium 282,385 282,260
Other reserves 42 36
Accumulated deficit (257,237) (256,530)
Shareholders' equity 29,271 29,843
Deferred license fees income 9,472 10,022
Finance lease liabilities 913 965
Other liabilities 7 15
Non-current liabilities 10,392 11,002
Deferred license fees income 2,200 2,200
Derivative financial liabilities 2,994 4,266
Trade and other payables 8,589 7,781
Finance lease liabilities 304 626
Current liabilities 14,087 14,873
Total equity and liabilities 53,750 55,718
CONSOLIDATED STATEMENT OF CASH FLOWS
For the first quarter ended 31 March
Q1 Q1
Amounts in EUR'000 2015 2014
Receipts from license partners, including
product sales 1,297 1,080
Receipt of Value Added Tax 261 204
Interest received 37 35
Other receipts - 122
Payments of third party fees and expenses,
including Value Added Tax (2,175) (1,654)
Payments of manufacturing expenses (1,976) (3,381)
Net compensation paid to (former) board members
and (former) employees (954) (516)
Payments of pension premiums, payroll taxes and
social securities, net of grants settled (524) (451)
Net cash flows from operating activities (4,034) (4,561)
Purchases of property, plant and equipment (70) -
Purchases of intangible assets - -
Net cash flows from investing activities (70) -
Proceeds of equity and warrants issued - 4,324
Payments of finance lease liabilities (413) (139)
Net cash flows from financing activities (413) 4,185
Increase/(decrease) of cash (4,517) (376)
Exchange rate effects 457 -
Cash and cash equivalents at 1 January 34,385 19,152
Total cash at 31 March 30,325 18,776
Of which restricted cash 200 176
Cash and cash equivalents at 31 March 30,125 18,600
Contact
Sijmen de Vries, CEO: T: +31-71-524-7400
FTI Consulting
Julia Phillips/ Victoria Foster Mitchell, T:
+44-203-727-1136
PRN NLD