1. LDX, currently marketed as VYVANSE in the US and
ELVANSE in certain territories in the EU for the treatment of
ADHD.
We enter 2013 in a good position following our strong
performance in 2012 and the investments we have made in previous
years. We anticipate that our highly differentiated portfolio will
deliver product sales growth in the low double digits.
We note the recent news of the approval of Barr's ANDA for
ADDERALL XR. We derive insignificant income from our authorised
generic supply contract with Barr (now owned by TEVA). We believe
that branded ADDERALL XR can continue to compete successfully in a
generic market as it has done over the last four years.
Royalties and other revenues are expected to be 30-40% lower
than 2012. This reflects a full year's impact of the lower ADDERALL
XR authorized generic royalty rate receivable from Impax, along
with generic competition and patent expiry on other products, and
the one-time $38 million of royalty
income recorded in Q4 2012 following the resolution of the
disagreement with GSK.
Our Non GAAP gross margin is expected to be at a similar level
to 2012.
We expect high single digit growth in combined Non GAAP R&D
and SG&A costs, with growth significantly weighted towards Non
GAAP R&D as we continue to invest in our promising pipeline and
progress our late stage clinical trials.
Our core effective tax rate on Non GAAP income is anticipated to
remain in the range of 18-20%.
As we look forward to the year ahead, we expect our financial
results to show further growth in line with current consensus
earnings expectations for 2013(1).
- Product sales in Q4 2012 were up 5% (up 5% on a CER basis) to
$1,098 million (Q4 2011: $1,049 million).
Product sales excluding ADDERALL XR were up 10% due to strong
growth particularly from VYVANSE (up 18% to $257 million), INTUNIV (up 24% to $81 million) and FIRAZYR(up 132% to $35 million). The growth in product sales
excluding ADDERALL XR was moderated by DERMAGRAFT® (down
65% to $19 million) due to the
ongoing restructuring of the Regenerative Medicine ("RM") sales and
marketing organization.
ADDERALL XR product sales were down 35% to $82 million primarily due to lower prescription
demand following the approval of a new generic version of ADDERALL
XR in Q2 2012, the accounting for the settlement of the Impax
litigation (see page 6 for further details) and higher sales
deductions.
- Total revenues were up 5% due to both higher product sales and
royalties. Royalties in Q4 2012 benefited from one-time royalty
income of $38 million for 3TC and
ZEFFIXfollowing the resolution of the disagreement with GSK and
ViiV.
- On a Non GAAP basis:
Operating income remained broadly constant at $368 million (Q4 2011: $369 million), as the increase in total revenues
was offset by higher Research and Development expenditure (up 14%)
as we continue to invest in a number of early and late stage
pipeline programs expected to drive future growth. The effect of
higher Research and Development expenditure was moderated by a
lower rate of increase in Selling, General and Administrative
expenditure (up 5%).
On a US GAAP basis:
Operating income was down 74% to $79
million (Q4 2011: $304
million) primarily due to charges to impair intangible
assets relating to RESOLOR in the EU of $171
million and higher legal and litigation costs in Q4 2012,
including a charge of $58 million in
relation to the agreement in principle with the US
Government.
- Non GAAP diluted earnings per ADS increased 4% to $1.58 (Q4 2011: $1.51) as broadly constant Non GAAP operating
income benefited from a lower effective tax rate on Non GAAP income
of 15% (Q4 2011: 19%).
On a US GAAP basis diluted earnings per ADS decreased 83% to
$0.22 (Q4 2011: $1.33), due to lower US GAAP operating income
together with a higher US GAAP effective tax rate of 35% (Q4 2011:
14%).
- Cash generation, a Non GAAP measure, increased by 1% to
$452 million (Q4 2011: $447 million).
Free cash flow, also a Non GAAP measure, decreased by 11% to
$314 million (Q4 2011: $351 million) primarily due to higher cash tax
payments in the quarter.
On a US GAAP basis, net cash provided by operating activities was
down 9% to $372 million (Q4 2011:
$409 million).
FOURTH QUARTER 2012 AND RECENT PRODUCT
AND PIPELINE DEVELOPMENTS
Products
ELVANSE® (LDX) for the treatment of Attention Deficit
Hyperactivity Disorder ("ADHD") in Europe
- On December 18, 2012 Shire
announced a positive outcome from the European Decentralized
Procedure for ELVANSE (to be known as TYVENSE® in
Ireland). ELVANSE is indicated as
part of a comprehensive treatment program for ADHD in children aged
6 years of age and over when response to previous methylphenidate
treatment is considered clinically inadequate.
Pipeline
LDX for the treatment of Binge Eating Disorder ("BED")
- A Phase 3 clinical program to evaluate the efficacy and safety
of LDX in adults with BED was initiated in Q4 2012.
LDX for the treatment of Negative Symptoms of Schizophrenia
("NSS")
- A Phase 3 clinical program to evaluate the efficacy and safety
of LDX as adjunctive treatment to antipsychotic medications on
negative symptoms in adults who have persistent predominant NSS was
initiated in Q4 2012.
FIRAZYR for the treatment for Angiotensin Converting Enzyme
Inhibitor-Induced Angioedema ("ACE-I AE")
- In December 2012, Shire submitted
a supplemental Marketing Authorization Application to the European
Medicines Agency ("EMA") seeking approval for FIRAZYR for the
treatment of ACE-I AE in Europe.
Depending upon the outcome of discussions with the US Food and Drug
Administration ("FDA") about appropriate development pathways for
FIRAZYR as a possible ACE-I AE treatment option, Phase 3 studies
for the US market could begin in 2013.
VPRIV for the treatment of Gaucher disease (Type 1)
- In December 2012, Shire filed
with the EMA in Europe for the
VPRIV label to be updated with data regarding the impact of VPRIV
on certain parameters of bone disease in Type 1 Gaucher
patients.
HGT2310 for the treatment of Hunter Syndrome with Central
Nervous System ("CNS") symptoms, idursulfase-IT
- HGT2310 is in development as an Enzyme Replacement Therapy
("ERT") delivered intrathecally for Hunter Syndrome patients with
CNS symptoms. Shire initiated a Phase 1/2 clinical trial in Q1 2010
which has now completed. The top line results of this trial
indicate that HGT2310 appears to be well tolerated at all three
doses studied during the timeframe of the trial. Furthermore,
dose-dependent drug activity in vivo was evidenced by a decline in
glycosaminoglycan ("GAG") levels in cerebrospinal fluid following
treatment, a biomarker of metabolic activity. Full results from
this trial will be presented at the American College of Medical
Genetics ("ACMG") meeting in March
2013. Shire is currently planning a pivotal clinical trial
which is expected to initiate in the second half of 2013, subject
to customary regulatory interactions with the FDA and EMA.
HGT1410 for Sanfilippo A Syndrome (Mucopolysaccharidosis
IIIA)
- HGT1410 is in development as an ERT delivered intrathecally for
the treatment of Sanfilippo A Syndrome (Mucopolysaccharidosis
IIIA). Shire initiated a Phase 1/2 clinical trial in August 2010 which has now completed. The top line
results of this trial indicate that HGT1410 appears to be well
tolerated at all three doses studied during the timeframe of the
trial. Furthermore, dose-dependent drug activity in vivo was
evidenced by a decline in GAG levels in cerebrospinal fluid
following treatment. Full results from this trial will be presented
at the ACMG meeting in March 2013.
Shire is currently planning the next clinical trial for HGT1410,
designed to measure a clinical response, which is expected to
initiate in the second half of 2013, subject to customary
regulatory interactions with the FDA and EMA.
ABH001 for the treatment of Epidermolysis Bullosa ("EB")
- In February 2013, Shire enrolled
the first patient in its Phase 3 clinical program for EB.
OTHER DEVELOPMENTS
Legal Proceedings
Shire reaches agreement in principle with the US Government
- On February 1, 2013 Shire
announced that it had reached an agreement in principle to resolve
the previously disclosed civil investigation into Shire's U.S.
sales and marketing practices relating to ADDERALL XR, VYVANSE and
DAYTRANA®. The agreement also addresses sales and
marketing practices relating to LIALDA® and
PENTASA® pursuant to a subsequent voluntary disclosure
made by Shire. Shire has recorded a $57.5
million charge in Q4 2012, comprised of the agreement in
principle amount, interest and costs. The agreement in principle is
subject to change until this matter is finally resolved.
Discussions between Shire and the US Government are ongoing to
establish a final resolution to the investigation.
Settlement of litigation with Impax
- On February 7, 2013 Shire and
Impax settled all litigation relating to Shire's contract to supply
Impax with authorized generic ADDERALL XR.
Under the terms of the settlement Shire will make a one-time cash
payment to Impax of $48.0 million and
Shire and Impax entered into an amended supply agreement which will
govern the supply of authorized generic ADDERALL XR from Shire to
Impax until the end of the supply term on September 30, 2014. The cash payment has been
recorded as a liability at December 31,
2012. As it represents a payment to a customer, the cash
payment has been recorded in the Income Statement as a reduction in
reported ADDERALL XR product sales ($42.0
million) and royalties ($6.0
million) in 2012, in accordance with US GAAP. The reduction
to revenues for Q4 2012 was $8.0
million, with the balance having been recorded in earlier
periods.
Collective dismissal and business
closure at Turnhout
- On January 23, 2013 Shire
announced that it had decided to proceed with a collective
dismissal and business closure at its site in Turnhout,
Belgium. This decision follows the
conclusion of an information and consultation process.
Shire will continue to sell RESOLOR in Europe and the supply of RESOLOR for patients
in Europe who rely on the medicine
will not be affected.
Acquisition of Lotus Tissue Repair,
Inc.
- On February 12, 2013 Shire
completed the acquisition of Lotus Tissue Repair, Inc. of
Cambridge, MA, a privately held
biotechnology company developing the first and only protein
replacement therapy currently being investigated for the treatment
of dystrophic epidermolysis bullosa ("DEB"). DEB is a devastating
orphan disease for which there is no currently approved treatment
option other than palliative care. Shire purchased the company for
an upfront cash payment and further contingent cash payments may be
payable in future periods, depending on the achievement of certain
safety and development milestones.
Leadership Team Changes
- We announce today that Sylvie
Gregoire, President of our HGT business will leave Shire at
the end of March after five years with the Company. Sylvie has
contributed to the growth of Shire through leading the building of
our rare diseases business; we're grateful for her significant
contributions and we wish her well in the future. Flemming Ørnskov
will assume interim leadership of this business from the end of
March. Mike Yasick, who for the last
five years has led Shire's largest business unit, Behavioral
Health, will assume interim leadership of the SP business from the
end of March.
- On November 15, 2012 Shire
announced that Dr. Jeff Jonas had
been appointed as President of Shire's RM business and has joined
the Shire Leadership Team. Jeff has been closely involved with the
RM business since Shire acquired it as Advanced BioHealing Inc.
("ABH") in June 2011. In addition to
his role as head of the SP R&D team, Jeff has been leading the
RM R&D team and has been a member of the RM leadership team. As
previously announced, Kevin Rakin,
who led ABH since 2007 and during its integration into Shire, has
stepped down from his position as RM President and from the Shire
Leadership Team to pursue new career interests.
Share buy-back Program
- Shire has a strong balance sheet and continued robust cash
generation, and considers efficient use of capital on behalf of
shareholders an important objective. Therefore in Q4 2012 Shire
commenced a share buy-back program, for the purpose of returning
funds to shareholders, of up to $500
million, through both direct purchases of ordinary shares
and through the purchase of ordinary shares underlying American
Depositary Receipts. As of February 13,
2013 Shire had made on-market repurchases totaling 4,776,274
ordinary shares at a cost of $143
million (excluding transaction costs).
For the weighted average number of shares used for Non GAAP diluted
earnings per ADS, please refer to the Non GAAP reconciliation
tables on pages 23 - 26.
DIVIDEND
In respect of the six months ended December 31, 2012 the Board has resolved to pay
an interim dividend of 14.60 US cents per ordinary share (2011:
12.59 US cents per ordinary share).
Dividend payments will be made in Pounds Sterling to ordinary
shareholders and in US Dollars to holders of ADSs. A dividend of
9.39 pence per ordinary share (2011:
7.96 pence) and 43.80 US cents per
ADS (2011: 37.77 US cents) will be paid on April 9, 2013 to shareholders on the register as
at the close of business on March 8,
2013.
Together with the first interim payment of 2.73 US cents per
ordinary share (2011: 2.48 US cents per ordinary share), this
represents total dividends for 2012 of 17.33 US cents per ordinary
share (2011: 15.07 US cents per ordinary share), an increase of 15%
in US Dollar terms.
ADDITIONAL INFORMATION
The following additional information is included in this press
release:
Page
Overview of Full Year 2012 Financial Results 9
Financial Information 14
Non GAAP Reconciliation 23
Notes to Editors 27
Safe Harbor Statement 28
Explanation of Non GAAP Measures 28
Trademarks 29
Dial in details for the live conference
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February 14, 2013:
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Live Webcast: http://www.shire.com/shireplc/en/investors
OVERVIEW OF FULL YEAR 2012 FINANCIAL
RESULTS
1. Product sales
For the year to December 31, 2012
product sales increased by 12% to $4,406.7
million (2011: $3,950.2
million) and represented 94% of total revenues (2011:
93%).
US Exit
Year on year growth Market
Product sales Sales $M Sales CER US Rx(1) Share(1)
VYVANSE 1,029.8 +28% +28% +17% 17%
ELAPRASE(R) 497.6 +7% +11% n/a(2) n/a(2)
REPLAGAL(R) 497.5 +5% +10% n/a(3) n/a(3)
LIALDA/MEZAVANT(R) 399.9 +7% +8% +5% 22%
VPRIV 306.6 +20% +23% n/a(2) n/a(2)
INTUNIV 287.8 +29% +29% +34% 5%
PENTASA 265.8 +6% +6% -5% 14%
FOSRENOL(R) 172.0 +3% +6% -19% 4%
DERMAGRAFT(4) 153.8 +46% +46% n/a(2) n/a(2)
FIRAZYR 116.3 +252% +258% n/a(2) n/a(2)
OTHER 250.6 -5% -2% n/a n/a
Excluding ADDERALL XR 3,977.7 +16% +18%
ADDERALL XR 429.0 -19% -19% -11% 5%
Total 4,406.7 +12% +13%
(1) Data provided by IMS Health National Prescription Audit ("IMS NPA"). Exit market
share represents the average US market share in the month ended December 31, 2012.
(2) IMS NPA Data not available.
(3) Not sold in the US in 2012.
(4) DERMAGRAFT was acquired by Shire on June 28, 2011 (sales growth above reflects
full year 2012 sales compared to post acquisition sales for 2011).
VYVANSE - ADHD
VYVANSE product sales grew strongly (28%) in 2012 as a result of
higher prescription demand, due to growth in US ADHD market (+9%)
and VYVANSE's share of that market, and as a result of a price
increase taken in 2012. These positive factors, together with lower
sales deductions in 2012, more than offset the effect of higher
retailer destocking in 2012 compared to 2011 and some shipment
slippage at the end of the fourth quarter.
ELAPRASE - Hunter syndrome
Reported ELAPRASE sales growth (7%) was driven by an increase in
the number of patients on therapy. On a CER basis, ELAPRASE sales
grew by 11% as reported sales were held back by unfavorable foreign
exchange (amounting to approximately $20
million) primarily due to weaker European currencies in 2012
compared to 2011. The increase in ELAPRASE sales between Q3 and Q4
of 2012 was partly driven by the timing of certain large orders
from markets which order less frequently.
REPLAGAL - Fabry disease
Reported REPLAGAL sales growth (5%) was driven by an increase in
the number of patients on therapy. On a CER basis, REPLAGAL sales
grew by 10%, as reported sales were impacted by unfavorable foreign
exchange (amounting to approximately $26
million), primarily due to weaker European currencies in
2012 compared to 2011. The reduction in REPLAGAL sales between the
third and fourth quarter of 2012 was partly driven by the timing of
certain large orders from markets which order less frequently.
LIALDA/MEZAVANT - Ulcerative
colitis
The growth in product sales for LIALDA/MEZAVANT (7%) in 2012 was
primarily driven by higher market share in the US and a price
increase taken since Q4 2011, the effects of which were partially
offset by product destocking in 2012 compared to a small amount of
product stocking in 2011 and higher sales deductions in 2012.
Growth in US net product sales was partially offset by the impact
of lower priced imports into certain European markets.
VPRIV - Gaucher disease
Reported VPRIV sales growth (20%) was driven by an increase in
the number of patients on therapy. On a CER basis, VPRIV sales
increased by 23% as reported sales were also held back by
unfavorable foreign exchange (amounting to approximately
$8 million).
INTUNIV - ADHD
INTUNIV product sales were up 29% compared to 2011, primarily
driven by strong growth in US prescription demand (up 34% compared
to 2011), together with price increases taken during 2012. These
positive factors were partially offset by lower stocking in 2012
and higher sales deductions in 2012 compared to 2011.
PENTASA - Ulcerative colitis
PENTASA product sales were up 6% as the benefit of price
increases was partially offset by lower prescription demand, a
small amount of destocking in 2012 and higher sales deductions as
compared to 2011.
FOSRENOL - Hyperphosphatemia
Product sales of FOSRENOL in the US increased (3%) due to the
effect of price increases in 2012 and lower sales deductions
compared to 2011, which more than offset the decline in
prescription demand. Product sales of FOSRENOL outside the US
decreased marginally primarily because of the impact of unfavorable
foreign exchange.
DERMAGRAFT - Diabetic Foot Ulcers
("DFU")
DERMAGRAFT product sales were up 46%(1) compared to
sales reported by Shire subsequent to acquisition in 2011. On a
full year basis, sales for DERMAGRAFT were down 21% reflecting the
impact of an ongoing restructuring of the RM sales and marketing
organization and the implementation of a new commercial model, all
of which is expected to position DERMAGRAFT for future sales
growth.
- Shire acquired DERMAGRAFT through its acquisition of ABH on
June 28, 2011 and reported revenues
from DERMAGRAFT of $105.3m relating
to the post acquisition period in 2011.
FIRAZYR - Hereditary Angioedema
Reported FIRAZYR sales growth (252%) was driven largely by the
first full year of sales in the US market, following launch of
FIRAZYR in the market in Q4 2011.
ADDERALL XR - ADHD
ADDERALL XR product sales decreased (-19%) in 2012 as a result
of lower US prescription demand following the introduction of a new
generic competitor and the impact of the accounting for the legal
settlement with Impax, which reduced reported product sales by
$42 million in 2012, in addition to
the effect of product destocking in 2012 compared to stocking in
2011 and, higher sales deductions. These negative factors were
partially offset by the benefit of a price increase taken during
2012.
2. Royalties
Product Royalties to Shire $M Year on year growth CER
3TC and ZEFFIX 91.6 +11% +11%
ADDERALL XR 70.3 -34% -34%
FOSRENOL 53.3 +15% +15%
Other 26.4 -44% -42%
Total 241.6 -15% -15%
Royalties from 3TC and ZEFFIX include one-time royalty income of
$38 million in respect of prior
periods due to resolution of the disagreement between Shire, GSK
and ViiV as to how the royalty rate for these products should be
applied. This one-time income more than offset the underlying
decline in 3TC and Zeffix royalties as a result of increased
competition and the expiry of patents in certain territories in
2012.
Royalties from ADDERALL XR in 2012 were significantly impacted
by the lower royalty rate payable on sales of authorized generic
ADDERALL XR by Impax, following the launch of a new generic version
of ADDERALL XR in late Q2 2012.
FOSRENOL royalties increased primarily due to higher royalties
received on sales in Japan.
Other royalties decreased primarily due to increased generic
competition.
3. Financial details
Cost of product sales
2012 % of 2011 % of
product product
$M sales $M sales
Cost of product sales (US GAAP) 645.4 15% 588.1 15%
Transfer of manufacturing from Owings Mills - (11.3)
Unwind of inventory fair value adjustment - (11.0)
Depreciation (31.5) (33.2)
Non GAAP Cost of product sales 613.9 14% 532.6 13%
Non GAAP cost of product sales as a percentage of product sales
increased slightly in 2012 primarily due to slight dilution from
DERMAGRAFT following the acquisition of ABH in Q2 2011.
US GAAP cost of product sales as a percentage of product sales
remained constant as the impact of lower Non GAAP gross margins in
2012 was offset by the fair value adjustment relating to DERMAGRAFT
inventories and costs incurred on the transfer of manufacturing
from Owings Mills in 2011 which were not repeated in 2012.
Research and Development
("R&D")
2012 % of 2011 % of
product product
$M sales $M sales
R&D (US GAAP) 965.5 22% 770.7 20%
Impairment of intangible assets (71.2) (16.0)
Payment in respect of in-licensed and
acquired products (23.0) -
Depreciation (22.5) (25.2)
Non GAAP R&D 848.8 19% 729.5 18%
Non GAAP R&D increased by $119.3
million, or 16%, due to our continuing investment in a
number of targeted R&D programs, particularly new uses for LDX
and recently acquired assets including SPD602 for iron overload
(acquired with FerroKin Biosciences Inc. ("FerroKin")). R&D
costs also include the first full year of RM's R&D
expenditure.
US GAAP R&D increased by $194.8
million, or 25%, a higher rate of increase than on a Non
GAAP basis as 2012 included higher in-process R&D ("IPR&D")
impairment charges relating to RESOLOR EU intangible assets and
up-front payments in respect of in-licensed and acquired
products.
Selling, General and Administrative
("SG&A")
2012 % of 2011 % of
product product
$M sales $M sales
SG&A (US GAAP) 2,114.0 48% 1,751.4 44%
Intangible asset amortization (194.1) (165.0)
Impairment of intangible assets (126.7) -
Legal and litigation costs(1) (102.6) -
Depreciation (59.8) (63.1)
Non GAAP SG&A 1,630.8 37% 1,523.3 39%
(1) In Q2 2012 Shire amended its Non GAAP policy to exclude costs related to the
settlement of litigation, government investigations and other disputes, together
with related external legal costs. Non GAAP SG&A in 2011 has not been restated as
the amounts incurred in that period were not significant.
Non GAAP SG&A increased by $107.5
million, or 7%, as we continue to invest in our business to
support our growth objectives. Non GAAP SG&A also included the
first full year of RM's SG&A expenditure. Reported costs
benefited (by 2 percentage points) from the stronger US Dollar in
2012.
US GAAP SG&A increased by $362.6
million, or 21%, a higher rate of increase than on a Non
GAAP basis, as 2012 included higher intangible asset amortization,
the impact of impairment charges and higher legal and litigation
costs, which included a charge of $57.5
million in relation to the agreement in principle with the
US Government and settling the litigation related to the
termination of co-promotion agreement for VYVANSE.
Impairment charges relate to RESOLOR intangible assets as the
actual and projected performance for RESOLOR has been adversely
affected by the challenging European reimbursement environment.
Shire has evaluated alternative sales and marketing strategies for
RESOLOR in response to these challenges but has judged that
projected profitability levels will continue to be below the level
forecast at the time of the acquisition of Movetis N.V.
("Movetis").
Gain on sale of product rights
For the year to December 31, 2012
Shire recorded a gain on sale of product rights of $18.1 million (2011: loss of $6.0 million) following re-measurement of the
contingent consideration receivable from the divestment of
DAYTRANA.
Integration and acquisition costs
For the year to December 31, 2012
Shire recorded integration and acquisition costs of $25.2 million (2011: $13.7
million), primarily associated with the acquisition of
FerroKin and the integration of ABH. In 2011 integration and
acquisition costs primarily related to the acquisition of ABH.
Interest expense
For the year to December 31, 2012
Shire incurred interest expense of $38.2
million (2011: $39.1 million).
Interest expense principally relates to the coupon and amortization
of issue costs on Shire's $1,100
million 2.75% convertible bonds due 2014.
Taxation
The effective tax rate on Non GAAP income in 2012 was 18% (2011:
22%) and the effective tax rate on US GAAP income was 18% (2011:
21%). The effective tax rate on both Non GAAP and US GAAP income in
2012 is lower than 2011 due to favorable changes in profit mix and
the benefit of the recognition of foreign tax credits.
FINANCIAL INFORMATION
TABLE OF CONTENTS
Page
Unaudited US GAAP Consolidated Balance Sheets 15
Unaudited US GAAP Consolidated Statements of Income 16
Unaudited US GAAP Consolidated Statements of Cash
Flows 18
Selected Notes to the Unaudited US GAAP Financial
Statements
(1) Earnings per share 20
(2) Analysis of revenues 21
Non GAAP reconciliation 23
Unaudited US GAAP financial position as of December 31, 2012
Consolidated Balance Sheets
December 31, December 31,
2012 2011
$M $M
ASSETS
Current assets:
Cash and cash equivalents 1,482.2 620.0
Restricted cash 17.1 20.6
Accounts receivable, net 824.2 845.0
Inventories 436.9 340.1
Deferred tax asset 229.9 207.6
Prepaid expenses and other current assets 221.8 174.9
Total current assets 3,212.1 2,208.2
Non-current assets:
Investments 38.7 29.9
Property, plant and equipment ("PP&E"), net 955.8 932.1
Goodwill 644.5 592.6
Other intangible assets, net 2,388.1 2,493.0
Deferred tax asset 46.5 50.7
Other non-current assets 31.5 73.7
Total assets 7,317.2 6,380.2
LIABILITIES AND EQUITY
Current liabilities:
Accounts payable and accrued expenses 1,501.5 1,370.5
Convertible bonds - 1,100.0
Other current liabilities 144.1 63.8
Total current liabilities 1,645.6 2,534.3
Non-current liabilities:
Convertible bonds 1,100.0 -
Deferred tax liability 520.8 516.6
Other non-current liabilities 241.6 144.3
Total liabilities 3,508.0 3,195.2
Equity:
Common stock of 5p par value; 1,000 million
shares authorized; and 562.5 million shares
issued and outstanding (2011: 1,000 million
shares authorized; and 562.5 million shares
issued and outstanding) 55.7 55.7
Additional paid-in capital 2,981.5 2,853.3
Treasury stock: 10.7 million shares (2011: 11.8
million) (310.4) (287.2)
Accumulated other comprehensive income 86.9 60.3
Retained earnings 995.5 502.9
Total equity 3,809.2 3,185.0
Total liabilities and equity 7,317.2 6,380.2
Unaudited US GAAP results for the three months and year to
December 31, 2012
Consolidated Statements of Income
3 months to 3 months to Year to Year to
December 31, December 31, December 31, December 31,
2012 2011 2012 2011
$M $M $M $M
Revenues:
Product sales 1,097.6 1,049.2 4,406.7 3,950.2
Royalties 87.2 83.7 241.6 283.5
Other revenues 16.4 9.3 32.9 29.7
Total revenues 1,201.2 1,142.2 4,681.2 4,263.4
Costs and expenses:
Cost of product sales(1) 166.6 153.4 645.4 588.1
R&D(1) 281.9 214.4 965.5 770.7
SG&A(1) 665.6 456.1 2,114.0 1,751.4
(Gain)/loss on sale of product rights (1.6) 2.2 (18.1) 6.0
Reorganization costs - 6.3 - 24.3
Integration and acquisition costs 10.1 5.8 25.2 13.7
Total operating expenses 1,122.6 838.2 3,732.0 3,154.2
Operating income 78.6 304.0 949.2 1,109.2
Interest income 0.8 0.4 3.1 1.9
Interest expense (9.2) (10.3) (38.2) (39.1)
Other (expense)/income, net (6.3) 2.2 (2.7) 18.1
Total other expense, net (14.7) (7.7) (37.8) (19.1)
Income before income taxes
and equity in earnings/(losses)
of equity method investees 63.9 296.3 911.4 1,090.1
Income taxes (22.4) (40.3) (167.0) (227.6)
Equity in earnings/(losses) of
equity method investees, net of taxes 0.5 (0.7) 1.0 2.5
Net income 42.0 255.3 745.4 865.0
(1) Cost of product sales includes amortization of intangible assets relating to
favorable manufacturing contracts of $nil for the three months to December 31, 2012
(2011: $0.4 million) and $0.7 million for the year to December 31, 2012 (2011:
$1.7 million). R&D includes intangible asset impairment charges of $44.2 million
(2011: $nil) for the three months to December 31, 2012 and $71.2 million (2011:
$16.0 million) for the year to December 31, 2012. SG&A costs include amortization
and impairment charges of intangible assets relating to intellectual property
rights acquired of $174.2 million for the three months to December 31, 2012
(2011: $45.9 million) and $320.8 million for the year to December 31, 2012 (2011:
$165.0 million).
Unaudited US GAAP results for the three months and year to
December 31, 2012
Consolidated Statements of Income (continued)
3 months to 3 months to Year to Year to
December 31, December 31, December 31, December 31,
2012 2011 2012 2011
Earnings per ordinary share - basic 7.5c 46.4c 134.2c 156.9c
Earnings per ADS - basic 22.5c 139.2c 402.6c 470.7c
Earnings per ordinary share - diluted 7.4c 44.4c 130.9c 150.9c
Earnings per ADS - diluted 22.2c 133.2c 392.7c 452.7c
Weighted average number of shares:
Millions Millions Millions Millions
Basic 555.2 550.7 555.4 551.1
Diluted(1) 558.5 593.9 593.5 595.4
(1) For the weighted average number of shares used for Non GAAP diluted earnings per
ADS, please refer to the Non GAAP reconciliation tables on pages 23 - 26.
Unaudited US GAAP results for the three months and year to
December 31, 2012
Consolidated Statements of Cash Flows
3 months to Year to
December 31, December 31,
2012 2011 2012 2011
$M $M $M $M
CASH FLOWS FROM OPERATING ACTIVITIES:
Net income 42.0 255.3 745.4 865.0
Adjustments to reconcile net income to net
cash provided by operating activities:
Depreciation and amortization 77.1 82.6 308.6 294.8
Share based compensation 22.1 21.0 87.1 75.7
Impairment of intangible assets 170.9 - 197.9 16.0
Gain on sale of non-current investments (0.2) - (0.5) (23.5)
(Gain)/loss on sale of product rights (1.6) 2.2 (18.1) 6.0
Other 12.6 10.2 18.0 16.1
Movement in deferred taxes (27.9) (1.3) (58.3) (14.5)
Equity in (earnings)/losses of
equity method investees (0.5) 0.7 (1.0) (2.5)
Changes in operating assets and liabilities:
Decrease/(increase) in accounts receivable 45.2 (11.3) 22.2 (134.0)
Increase in sales deduction accrual 6.6 34.3 42.7 80.5
Increase in inventory (6.3) (21.6) (88.2) (64.4)
Increase in prepayments and other assets (32.3) (54.1) (14.5) (36.8)
Increase/(decrease) in accounts
payable and other liabilities 64.0 91.4 136.7 (10.0)
Returns on investment from joint venture - - 4.9 5.2
Net cash provided by operating activities (A) 371.7 409.4 1,382.9 1,073.6
CASH FLOWS FROM INVESTING ACTIVITIES:
Movements in restricted cash 1.8 0.5 3.5 6.2
Purchases of subsidiary undertakings and
businesses, net of cash acquired - (1.5) (97.0) (725.0)
Purchases of non-current investments (5.9) (2.4) (18.0) (10.7)
Purchases of PP&E (58.0) (58.4) (149.6) (194.3)
Purchases of intangible assets - - (43.5) (5.2)
Proceeds from disposal of non-current
investments and PP&E 2.6 11.3 7.2 106.0
Proceeds from capital expenditure grants - - 8.4 -
Proceeds received on sale of product rights 4.1 3.2 17.8 12.0
Returns of equity investments and
proceeds from short term investments - 0.1 0.2 1.8
Net cash used in investing activities (B) (55.4) (47.2) (271.0) (809.2)
Unaudited US GAAP results for the three months and year to
December 31, 2012
Consolidated Statements of Cash Flows (continued)
3 months to Year to
December 31, December 31,
2012 2011 2012 2011
$M $M $M $M
CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from drawing of revolving
credit facility - - - 30.0
Repayment of revolving credit facility - - - (30.0)
Repayment of debt acquired through
business combinations - - (3.0) (13.1)
Excess tax benefit associated with
exercise of stock options 2.1 7.7 40.7 31.4
Payments to acquire shares under the share
buy-back program (106.5) - (106.5) -
Payments to acquire shares by the
Employee Benefit Trust ("EBT") (48.4) (25.0) (99.3) (151.8)
Proceeds from exercise of options 15.6 12.5 16.2 13.4
Deferred contingent consideration payments (2.9) - (5.8) -
Payment of dividend (15.6) (13.3) (86.3) (73.8)
Other - (0.5) (0.3) (1.5)
Net cash used in financing activities (C) (155.7) (18.6) (244.3) (195.4)
Effect of foreign exchange rate changes on
cash and cash equivalents (D) (0.3) - (5.4) 0.4
Net increase in cash and cash equivalents
(A) + (B) + (C) + (D) 160.3 343.6 862.2 69.4
Cash and cash equivalents at
beginning of period 1,321.9 276.4 620.0 550.6
Cash and cash equivalents at
end of period 1,482.2 620.0 1,482.2 620.0
Unaudited US GAAP results for the three months
and year to December 31,
2012
Selected Notes to the Financial
Statements
(1) Earnings Per Share ("EPS")
3 months to 3 months to Year to Year to
December 31, December 31, December 31, December 31,
2012 2011 2012 2011
$M $M $M $M
Numerator for basic EPS 42.0 255.3 745.4 865.0
Interest on convertible bonds,
net of tax (1) - 8.4 31.3 33.6
Numerator for diluted EPS 42.0 263.7 776.7 898.6
Weighted average number of shares:
Millions Millions Millions Millions
Basic(2) 555.2 550.7 555.4 551.1
Effect of dilutive shares:
Share based awards to employees(3) 3.3 9.7 4.6 10.9
Convertible bonds 2.75% due 2014(4) - 33.5 33.5 33.4
Diluted(5) 558.5 593.9 593.5 595.4
(1) For the three month period ended December 31, 2012 interest on the convertible
bond has not been added back as the effect would be anti-dilutive
(2) Excludes shares purchased by the EBT and under the share buy-back program and
presented by Shire as treasury stock.
(3) Calculated using the treasury stock method.
(4) Calculated using the "if converted" method.
(5) For the weighted average number of shares used for Non GAAP diluted earnings per
ADS, please refer to the Non GAAP reconciliation tables on pages 23 - 26.
The share equivalents not included in the calculation of the
diluted weighted average number of shares are shown below:
3 months to 3 months to Year to Year to
December 31, December 31, December 31, December 31,
2012 2011 2012 2011
Millions Millions Millions Millions
Share based awards to employees(1) 6.7 2.7 5.2 2.9
Convertible bonds 2.75% due 2014(2) 33.5 - - -
(1) Certain stock options have been excluded from the calculation of diluted EPS
because (a) their exercise prices exceeded Shire's average share price during the
calculation period or (b) the required performance conditions were not satisfied
as at the balance sheet date.
(2) For the three month period ended December 31, 2012 the ordinary shares underlying
the convertible bonds have not been included in the calculation of the diluted
weighted average number of shares, as the effect of their inclusion would be
anti-dilutive.
Unaudited US GAAP results for the year
to December 31,
2012
Selected Notes to the Financial
Statements
(2) Analysis of revenues
Year to December 31, 2012 2011 2012 2012
% % of total
$M $M change revenue
Net product sales:
Specialty Pharmaceuticals
Behavioral Health
VYVANSE 1,029.8 805.0 28% 22%
ADDERALL XR 429.0 532.8 -19% 9%
INTUNIV 287.8 223.0 29% 6%
EQUASYM(R) 29.2 19.9 47% 1%
1,775.8 1,580.7 12% 38%
Gastro Intestinal
LIALDA/MEZAVANT 399.9 372.1 7% 9%
PENTASA 265.8 251.4 6% 6%
RESOLOR 11.8 6.1 93% <1%
677.5 629.6 8% 15%
General products
FOSRENOL 172.0 166.9 3% 4%
XAGRID(R) 97.2 90.6 7% 2%
269.2 257.5 5% 6%
Other product sales 112.4 147.8 -24% 2%
Total SP product sales 2,834.9 2,615.6 8% 61%
Human Genetic Therapies
ELAPRASE 497.6 464.9 7% 11%
REPLAGAL 497.5 475.2 5% 11%
VPRIV 306.6 256.2 20% 6%
FIRAZYR 116.3 33.0 252% 2%
Total HGT product sales 1,418.0 1,229.3 15% 30%
Regenerative Medicine
DERMAGRAFT 153.8 105.3 46% 3%
Total RM product sales 153.8 105.3 46% 3%
Total product sales 4,406.7 3,950.2 12% 94%
Royalties:
3TC and ZEFFIX 91.6 82.7 11% 2%
ADDERALL XR 70.3 107.1 -34% 2%
FOSRENOL 53.3 46.5 15% 1%
Other 26.4 47.2 -44% <1%
Total royalties 241.6 283.5 -15% 5%
Other revenues 32.9 29.7 11% 1%
Total revenues 4,681.2 4,263.4 10% 100%
Unaudited US GAAP results for the three months
to December 31,
2012
Selected Notes to the Financial
Statements
(2) Analysis of revenues
3 months to December 31, 2012 2011 2012 2012
% % of total
$M $M change revenue
Net product sales:
Specialty Pharmaceuticals
Behavioral Health
VYVANSE 256.5 217.1 18% 21%
ADDERALL XR 81.5 124.8 -35% 7%
INTUNIV 81.2 65.4 24% 7%
EQUASYM 7.9 4.3 84% 1%
427.1 411.6 4% 36%
Gastro Intestinal
LIALDA/MEZAVANT 111.4 96.1 16% 9%
PENTASA 69.1 65.2 6% 6%
RESOLOR 3.5 2.1 67% <1%
184.0 163.4 13% 15%
General products
FOSRENOL 45.2 39.9 13% 4%
XAGRID 26.5 21.4 24% 2%
71.7 61.3 17% 6%
Other product sales 26.5 30.5 -13% 2%
Total SP product sales 709.3 666.8 6% 59%
Human Genetic Therapies
ELAPRASE 139.3 124.0 12% 12%
REPLAGAL 118.2 120.9 -2% 10%
VPRIV 77.3 69.3 12% 6%
FIRAZYR 34.6 14.9 132% 3%
Total HGT product sales 369.4 329.1 12% 31%
Regenerative Medicine
DERMAGRAFT 18.9 53.3 -65% 1%
Total RM product sales 18.9 53.3 -65% 1%
Total product sales 1,097.6 1,049.2 5% 91%
Royalties:
3TC and ZEFFIX 56.8 18.6 205% 5%
ADDERALL XR 8.1 40.5 -80% 1%
FOSRENOL 16.3 15.1 8% 1%
Other 6.0 9.5 -37% <1%
Total royalties 87.2 83.7 4% 7%
Other revenues 16.4 9.3 76% 2%
Total revenues 1,201.2 1,142.2 5% 100%
Unaudited results for the year to
December 31, 2012
Non GAAP reconciliation
Year to December 31, 2012 US GAAP Adjustments Non GAAP
(a) (b) (c) (d) (e)
$M $M $M $M $M $M $M
Total revenues 4,681.2 - - - - - 4,681.2
Costs and expenses:
Cost of product sales 645.4 - - - - (31.5) 613.9
R&D 965.5 (71.2) (23.0) - - (22.5) 848.8
SG&A 2,114.0 (320.8) - - (102.6) (59.8) 1,630.8
Gain on sale of product rights (18.1) - - 18.1 - - -
Integration and acquisition costs 25.2 - (25.2) - - - -
Depreciation - - - - - 113.8 113.8
Total operating expenses 3,732.0 (392.0) (48.2) 18.1 (102.6) - 3,207.3
Operating income 949.2 392.0 48.2 (18.1) 102.6 - 1,473.9
Interest income 3.1 - - - - - 3.1
Interest expense (38.2) - - - - - (38.2)
Other (expense)/income, net (2.7) 4.0 - - - - 1.3
Total other expense, net (37.8) 4.0 - - - - (33.8)
Income before income taxes and
equity in earnings of equity
method investees 911.4 396.0 48.2 (18.1) 102.6 - 1,440.1
Income taxes (167.0) (59.5) (9.9) - (28.3) - (264.7)
Equity in earnings of equity
method investees, net of tax 1.0 - - - - - 1.0
Net income 745.4 336.5 38.3 (18.1) 74.3 - 1,176.4
Impact of convertible debt,
net of tax 31.3 - - - - - 31.3
Numerator for diluted EPS 776.7 336.5 38.3 (18.1) 74.3 - 1,207.7
Weighted average number of shares
(millions) - diluted 593.5 - - - - - 593.5
Diluted earnings per ADS 392.7c 170.0c 19.4c (9.1c) 37.5c - 610.5c
The following items are included in Adjustments:
(a) Amortization and asset impairments: Impairment of IPR&D intangible assets for
RESOLOR in the EU ($71.2 million), impairment charges of intellectual property
rights acquired for RESOLOR in the EU ($126.7 million), amortization of intangible
assets relating to intellectual property rights acquired ($194.1 million),
impairment of available for sale securities ($4.0 million), and tax effect of
adjustments;
(b) Acquisitions and integration activities: Up-front payments made to Sangamo
Biosciences Inc. and for the acquisition of the US rights to prucalopride
(marketed in certain countries in Europe as RESOLOR) ($23.0 million), costs
primarily associated with the acquisition of FerroKin and the integration of ABH
($16.0 million), charges related to the change in fair value of deferred contingent
consideration ($9.2 million), and tax effect of adjustments;
(c) Divestments, reorganizations and discontinued operations: Re-measurement of
DAYTRANA contingent consideration to fair value ($18.1 million) and tax effect
of adjustments;
(d) Legal and litigation costs: Costs related to litigation, government investigations,
other disputes and external legal costs ($102.6 million), and tax effect of
adjustments; and
(e) Depreciation reclassification: Depreciation of $113.8 million included in Cost of
product sales, R&D costs and SG&A costs for US GAAP separately disclosed for the
presentation of Non GAAP earnings.
Unaudited results for the year to
December 31, 2011
Non GAAP reconciliation
Year to December 31, 2011 US GAAP Adjustments Non GAAP
(a) (b) (c) (d)
$M $M $M $M $M $M
Total revenues 4,263.4 - - - - 4,263.4
Costs and expenses:
Cost of product sales 588.1 - (11.0) (11.3) (33.2) 532.6
R&D 770.7 (16.0) - - (25.2) 729.5
SG&A 1,751.4 (165.0) - - (63.1) 1,523.3
Loss on sale of product rights 6.0 - - (6.0) - -
Reorganization costs 24.3 - - (24.3) - -
Integration and acquisition costs 13.7 - (13.7) - - -
Depreciation - - - - 121.5 121.5
Total operating expenses 3,154.2 (181.0) (24.7) (41.6) - 2,906.9
Operating income 1,109.2 181.0 24.7 41.6 - 1,356.5
Interest income 1.9 - - - - 1.9
Interest expense (39.1) - - - - (39.1)
Other income/(expense), net 18.1 2.4 - (23.5) - (3.0)
Total other expense, net (19.1) 2.4 - (23.5) - (40.2)
Income before income taxes and equity
in earnings of equity method investees 1,090.1 183.4 24.7 18.1 - 1,316.3
Income taxes (227.6) (58.7) (8.3) 2.7 - (291.9)
Equity in earnings of equity method
investees, net of tax 2.5 - - - - 2.5
Net income 865.0 124.7 16.4 20.8 - 1,026.9
Impact of convertible debt, net of tax 33.6 - - - - 33.6
Numerator for diluted EPS 898.6 124.7 16.4 20.8 - 1,060.5
Weighted average number of shares
(millions) - diluted 595.4 - - - - 595.4
Diluted earnings per ADS 452.7c 62.7c 8.4c 10.5c - 534.3c
The following items are included in Adjustments:
(a) Amortization and asset impairments: Impairment of intangible assets
($16.0 million), amortization of intangible assets relating to intellectual
property rights acquired ($165.0 million), impairment of available for sale
securities ($2.4 million), and tax effect of adjustments;
(b) Acquisitions and integration activities: Unwind of ABH inventory fair value
adjustment ($11.0 million), costs associated with acquisition and integration of
ABH ($13.6 million) and integration of Movetis ($8.3 million), less adjustment to
contingent consideration payable for EQUASYM ($8.2 million), and tax effect
of adjustments;
(c) Divestments, reorganizations and discontinued operations: Accelerated depreciation
($6.6 million) and dual running costs ($4.7 million) on the transfer of
manufacturing from Owings Mills to a third party, re-measurement of DAYTRANA
contingent consideration to fair value ($6.0 million), reorganization costs
($24.3 million) on the transfer of manufacturing from Owings Mills to a third
party and the establishment of an international commercial hub in Switzerland,
gain on disposal of investment in Vertex ($23.5 million), and tax effect of
adjustments; and
(d) Depreciation: Depreciation of $121.5 million included in Cost of product sales,
R&D costs and SG&A costs for US GAAP separately disclosed for the presentation
of Non GAAP earnings.
Unaudited results for the three
months to December 31, 2012
Non GAAP reconciliation
Non
3 months to December 31, 2012 US GAAP Adjustments GAAP
(a) (b) (c) (d) (e)
$M $M $M $M $M $M $M
Total revenues 1,201.2 - - - - - 1,201.2
Costs and expenses:
Cost of product sales 166.6 - - - - (7.9) 158.7
R&D 281.9 (44.2) - - - (4.2) 233.5
SG&A 665.6 (174.2) - - (62.2) (17.5) 411.7
Gain on sale of product rights (1.6) - - 1.6 - - -
Integration and acquisition costs 10.1 - (10.1) - - - -
Depreciation - - - - - 29.6 29.6
Total operating expenses 1,122.6 (218.4) (10.1) 1.6 (62.2) - 833.5
Operating income 78.6 218.4 10.1 (1.6) 62.2 - 367.7
Interest income 0.8 - - - - - 0.8
Interest expense (9.2) - - - - - (9.2)
Other expense, net (6.3) 4.0 - - - - (2.3)
Total other expense, net (14.7) 4.0 - - - - (10.7)
Income before income taxes and
equity in earnings of equity
method investees 63.9 222.4 10.1 (1.6) 62.2 - 357.0
Income taxes (22.4) (17.5) 0.2 - (13.8) - (53.5)
Equity in earnings of equity
method investees, net of tax 0.5 - - - - - 0.5
Net income 42.0 204.9 10.3 (1.6) 48.4 - 304.0
Impact of convertible debt,
net of tax (1) - 7.6 - - - - 7.6
Numerator for diluted EPS 42.0 212.5 10.3 (1.6) 48.4 - 311.6
Weighted average number of shares
(millions) - diluted (1) 558.5 33.5 - - - - 592.0
Diluted earnings per ADS 22.5c 106.5c 5.1c (0.9c) 24.6c - 157.8c
(1) The impact of convertible debt, net of tax has a dilutive effect on Non GAAP basis.
The following items are included in Adjustments:
(a) Amortization and asset impairments: Impairment of IPR&D intangible assets for
RESOLOR ($44.2 million), impairment charges of intellectual property rights
acquired for RESOLOR in the EU ($126.7 million), amortization of intangible
assets relating to intellectual property rights acquired ($47.5 million),
impairment of available for sale securities ($4.0 million), and tax effect of
adjustments;
(b) Acquisition and integration activities: Costs primarily associated with the
acquisition of FerroKin and the integration of ABH ($4.2 million), charges related
to the change in fair value of deferred contingent consideration ($5.9 million),
and tax effect of adjustments;
(c) Divestments, reorganizations and discontinued operations: Re-measurement of
DAYTRANA contingent consideration to fair value ($1.6 million), and tax effect
of adjustments;
(d) Legal and litigation costs: Costs related to litigation, government investigations,
other disputes and external legal costs ($62.2 million), and tax effect of
adjustments; and
(e) Depreciation reclassification: Depreciation of $29.6 million included in Cost of
product sales, R&D costs and SG&A costs for US GAAP separately disclosed for the
presentation of Non GAAP earnings.
Unaudited results for the three
months to December 31, 2011
Non GAAP reconciliation
3 months to December 31, 2011 US GAAP Adjustments Non GAAP
(a) (b) (c) (d)
$M $M $M $M $M $M
Total revenues 1,142.2 - - - - 1,142.2
Costs and expenses:
Cost of product sales 153.4 - (2.0) (2.3) (10.8) 138.3
R&D 214.4 - - - (8.8) 205.6
SG&A 456.1 (45.9) - - (16.7) 393.5
Loss on sale of product
rights 2.2 - - (2.2) - -
Reorganization costs 6.3 - - (6.3) - -
Integration and acquisition
costs 5.8 - (5.8) - - -
Depreciation - - - - 36.3 36.3
Total operating expenses 838.2 (45.9) (7.8) (10.8) - 773.7
Operating income 304.0 45.9 7.8 10.8 - 368.5
Interest income 0.4 - - - - 0.4
Interest expense (10.3) - - - - (10.3)
Other income/(expense), net 2.2 - - - - 2.2
Total other income/(expense),
net (7.7) - - - - (7.7)
Income before income taxes
and equity in earnings of
equity method investees 296.3 45.9 7.8 10.8 - 360.8
Income taxes (40.3) (23.1) (4.1) (1.8) - (69.3)
Equity in earnings of equity
method investees, net of tax (0.7) - - - - (0.7)
Net income 255.3 22.8 3.7 9.0 - 290.8
Impact of convertible debt,
net of tax 8.4 - - - - 8.4
Numerator for diluted EPS 263.7 22.8 3.7 9.0 - 299.2
Weighted average number of
shares (millions) - diluted 593.9 - - - - 593.9
Diluted earnings per ADS 133.2c 11.5c 1.9c 4.6c - 151.2c
The following items are included in Adjustments:
(a) Amortization and asset impairments: Amortization of intangible assets relating to
intellectual property rights acquired ($45.9 million), and tax effect of
adjustments;
(b) Acquisition and integration activities: Unwind of ABH inventory fair value
adjustment ($2.0 million), costs associated with the acquisition and integration
of ABH ($3.5 million) and integration of Movetis ($2.3 million), and tax effect
of adjustments;
(c) Divestments, reorganizations and discontinued operations: Dual running costs
($2.3 million) on the transfer of manufacturing from Owings Mills to a third party,
re-measurement of DAYTRANA contingent consideration to fair value ($2.2 million),
reorganization costs ($6.3 million) on the transfer of manufacturing from Owings
Mills to a third party and establishment of an international commercial hub in
Switzerland, and tax effect of adjustments; and
(d) Depreciation: Depreciation of $36.3 million included in Cost of product sales,
R&D costs and SG&A costs for US GAAP separately disclosed for the presentation of
Non GAAP earnings.
Unaudited results for the three
months and year to December 31,
2012
Non GAAP reconciliation
The following table reconciles US GAAP net cash provided by
operating activities to Non GAAP cash generation:
3 months to December 31, Year to December 31,
2012 2011 2012 2011
$M $M $M $M
Net cash provided by operating activities 371.7 409.4 1,382.9 1,073.6
Tax and interest payments, net 79.9 37.4 230.8 317.4
Up-front payments in respect of
in-licensed and acquired products - - 23.0 -
Non GAAP cash generation 451.6 446.8 1,636.7 1,391.0
The following table reconciles US GAAP net cash provided by
operating activities to Non GAAP free cash flow:
3 months to December 31, Year to December 31,
2012 2011 2012 2011
$M $M $M $M
Net cash provided by operating activities 371.7 409.4 1,382.9 1,073.6
Up-front payments in respect of
in-licensed and acquired products - - 23.0 -
Capital expenditure (58.0) (58.4) (149.6) (194.3)
Non GAAP free cash flow 313.7 351.0 1,256.3 879.3
Non GAAP net cash/(debt) comprises:
December 31, December 31,
2012 2011
$M $M
Cash and cash equivalents 1,482.2 620.0
Convertible bonds (1,100.0) (1,100.0)
Other debt (9.3) (8.2)
Non GAAP net cash/(debt) 372.9 (488.2)
NOTES TO EDITORS
Shire enables people with
life-altering conditions to lead better lives.
Through our deep understanding of patients' needs, we develop
and provide healthcare in the areas of:
- Behavioral Health and Gastro Intestinal conditions
- Rare Diseases
- Regenerative Medicine
as well as other symptomatic conditions treated by specialist
physicians.
We aspire to imagine and lead the future of healthcare, creating
value for patients, physicians, policymakers, payors and our
shareholders.
http://www.shire.com
THE "SAFE HARBOR" STATEMENT UNDER THE
PRIVATE SECURITIES LITIGATION REFORM ACT OF 1995
Statements included herein that are not historical facts are
forward-looking statements. Such forward-looking statements involve
a number of risks and uncertainties and are subject to change at
any time. In the event such risks or uncertainties materialize,
Shire's results could be materially adversely affected. The risks
and uncertainties include, but are not limited to, that:
- Shire's products may not be a commercial success;
- revenues from ADDERALL XR are subject to generic erosion;
- the failure to obtain and maintain reimbursement, or an
adequate level of reimbursement, by third party payors in a timely
manner for Shire's products may impact future revenues and
earnings;
- Shire relies on a single source for manufacture of certain of
its products and a disruption to the supply chain for those
products may result in Shire being unable to continue marketing or
developing a product or may result in Shire being unable to do so
on a commercially viable basis;
- Shire uses third party manufacturers to manufacture many of its
products and is reliant upon third party contractors for certain
goods and services, and any inability of these third party
manufacturers to manufacture products, or any failure of these
third party contractors to provide these goods and services, in
each case in accordance with its respective contractual
obligations, could adversely affect Shire's ability to manage its
manufacturing processes or to operate its business;
- the development, approval and manufacturing of Shire's products
is subject to extensive oversight by various regulatory agencies
and regulatory approvals or interventions associated with changes
to manufacturing sites, ingredients or manufacturing processes
could lead to significant delays, increase in operating costs, lost
product sales, an interruption of research activities or the delay
of new product launches;
- the actions of certain customers could affect Shire's ability
to sell or market products profitably and fluctuations in
buying or distribution patterns by such customers could adversely
impact Shire's revenues, financial conditions or results of
operations;
- investigations or enforcement action by regulatory authorities
or law enforcement agencies relating to Shire's activities in the
highly regulated markets in which it operates may result in the
distraction of senior management, significant legal costs and the
payment of substantial compensation or fines;
- adverse outcomes in legal matters and other disputes, including
Shire's ability to obtain, maintain, enforce and defend patents and
other intellectual property rights required for its business, could
have a material adverse effect on Shire's revenues, financial
condition or results of operations;
and other risks and uncertainties detailed from time to time in
Shire's filings with the Securities and Exchange Commission,
including those risks outlined in "Item 1A: Risk Factors" in
Shire's Form 10-K for the years ended December 31, 2011 and 2012.
Non GAAP Measures
This press release contains financial measures not prepared in
accordance with US GAAP. These measures are referred to as
"Non GAAP" measures and include: Non GAAP operating income; Non
GAAP net income; Non GAAP diluted earnings per ADS;
effectivetax rate on Non GAAP income before income taxes and
earnings/(losses) of equity method investees
("effective tax rate on Non GAAP
income"); Non GAAP cost of product sales; Non GAAP
research and development; Non GAAP selling, general and
administrative; Non GAAP other income/expense; Non GAAP cash
generation; Non GAAP free cash flow and Non GAAP net
cash/(debt). These Non GAAP measures exclude the effect of
certain cash and non-cash items, that Shire's management believes
are not related to the core performance of Shire's business.
These Non GAAP financial measures are used by Shire's management
to make operating decisions because they facilitate internal
comparisons of Shire's performance to historical results and to
competitors' results. Shire's Remuneration Committee uses
certain key Non GAAP measures when assessing the performance and
compensation of employees, including Shire's executive
directors.
The Non GAAP measures are presented in this press release as
Shire's management believe that they will provide investors with a
means of evaluating, and an understanding of how Shire's management
evaluates, Shire's performance and results on a comparable basis
that is not otherwise apparent on a US GAAP basis, since many
non-recurring, infrequent or non-cash items that Shire's management
believe are not indicative of the core performance of the business
may not be excluded when preparing financial measures under US
GAAP.
These Non GAAP measures should not be considered in isolation
from, as substitutes for, or superior to financial measures
prepared in accordance with US GAAP.
Where applicable the following items, including their tax
effect, have been excluded when calculating Non GAAP earnings for
both 2012 and 2011, and from our Outlook:
Amortization and asset
impairments:
- Intangible asset amortization and impairment charges; and
- Other than temporary impairment of investments.
Acquisitions and integration
activities:
- Up-front payments and milestones in respect of in-licensed and
acquired products;
- Costs associated with acquisitions, including transaction
costs, fair value adjustments on contingent consideration and
acquired inventory;
- Costs associated with the integration of companies; and
- Noncontrolling interests in consolidated variable interest
entities.
Divestments, re-organizations and
discontinued operations:
- Gains and losses on the sale of non-core assets;
- Costs associated with restructuring and re-organization
activities;
- Termination costs; and
- Income/(losses) from discontinued operations.
Legal and litigation costs:
- Net legal costs related to the settlement of litigation,
government investigations and other disputes (excluding internal
legal team costs).
Depreciation, which is included in Cost of product sales,
R&D and SG&A costs in our US GAAP results, has been
separately disclosed for the presentation of 2011 and 2012 Non GAAP
earnings.
Cash generation represents net cash provided by operating
activities, excluding up-front and milestone payments for
in-licensed and acquired products, tax and interest payments.
Free cash flow represents net cash provided by operating
activities, excluding up-front and milestone payments for
in-licensed and acquired products, but including capital
expenditure in the ordinary course of business.
A reconciliation of Non GAAP financial measures to the most
directly comparable measure under US GAAP is presented on pages 23
to 27.
Growth at CER, which is a Non GAAP measure, is computed by
restating 2012 results using average 2011 foreign exchange rates
for the relevant period.
Average exchange rates for the year to December 31, 2012 were $1.59:£1.00 and $1.29:€1.00 (2011: $1.60:£1.00 and $1.39:€1.00). Average exchange rates for Q4 2012
were $1.61:£1.00 and $1.29:€1.00 (2011: $1.57:£1.00 and $1.35:€1.00).
TRADE MARKS
All trade marks designated ® and ™ used in this press
release are trade marks of Shire plc or companies within the Shire
group except for 3TC® and ZEFFIX® which are
trade marks of GSK, PENTASA® which is a registered trade
mark of FERRING B.V., LIALDA® which is a trade mark of
Nogra International Limited, MEZAVANT® which is a trade
mark of Giuliani International Limited and DAYTRANA®
which is a trade mark of Noven Pharmaceuticals Inc. Certain trade
marks of Shire plc or companies within the Shire group are set out
in Shire's Annual Report on Form 10-K for the years ended
December 31, 2011 and 2012 and the
Quarterly Report on Form 10-Q for the three months and nine months
ended September 30, 2012.
For further information please
contact:
Investor Relations
- Eric Rojas, erojas@shire.com,
+1-781-482-0999
- Sarah Elton-Farr,
seltonfarr@shire.com, +44-1256-894-157
Media
- Jessica Mann (Corporate),
jmann@shire.com, +44-1256-894-280
- Gwen Fisher (Specialty Pharma),
gfisher@shire.com, +1-484-595-9836
- Jessica Cotrone (Human Genetic
Therapies), jcotrone@shire.com, +1-781-482-9538
- Lindsey Hart (Regenerative
Medicine), lhart@shire.com, +1-615-250-3311