Shire Proposes to Expand Specialist Gastrointestinal Portfolio

By Shire Plc, PRNE
Monday, August 2, 2010

Shire to Add Newly-Launched RESOLOR(R) and a Promising GI Pipeline to its GI Business Through Proposed Recommended Cash Acquisition of Movetis NV

DUBLIN, August 3, 2010 -

    - Proposed recommended cash acquisition of specialty gastrointestinal
      (GI) company Movetis NV for a fully diluted equity purchase price of
      EUR428 million in cash. As at March 31, 2010, their last reporting
      date, Movetis held EUR100 million in cash; based on this the
      enterprise value of Movetis (less cash) would be EUR328 million
    - Strong strategic fit with Shire's growing core GI business; RESOLOR(R)
      brings an additional approved GI medicine with strong patent
      protection addressing a symptomatic unmet need
    - The acquisition of Movetis is value and growth enhancing, will be
      earnings accretive after 2012, and adds immediate revenues from the
      recently launched RESOLOR to Shire's GI portfolio
    - Proposed acquisition of Movetis brings to Shire world-class research
      and development talent and a promising GI pipeline, offering additional
      opportunities that include two projects in early clinical development
      and several pre-clinical leads as well as the rights to a large library
      of qualified lead compounds with potential for development in different
      GI indications
    - Broadens Shire's international specialty product portfolio and further
      expands its ex-US business
    - Movetis has rights to RESOLOR in the 27 countries of the European
      Union, plus Iceland, Lichtenstein, Norway and Switzerland. RESOLOR is
      approved in 30 of these countries and is already launched in Germany
      and the UK. Shire anticipates further launches in other European
      countries in the next 12 months. Movetis is entitled to receive
      royalties on sales of RESOLOR outside of Europe from Johnson & Johnson
    - RESOLOR is a new chemical entity with composition of matter patent
      protection extending through 2020 and Shire estimates potential annual
      peak sales of over EUR300 million
    - The acquisition expands and complements Shire's commercial capability
      and longstanding expertise in the GI field
    - The acquisition of Movetis will be financed from Shire's existing cash
      resources
    - Institutional shareholders, holding in aggregate 38.9% of Movetis'
      issued share capital, have unconditionally agreed to accept the offer
      in respect of their own shares
    - Shire confirms that its business continues to perform very well. Given
      this strong performance there is no impact to previously stated
      guidance for 2010 due to the modest short term financial effect of
      the acquisition of Movetis. Shire will update its guidance when it
      announces its Second Quarter results on Wednesday August 4, 2010

Shire plc (LSE: SHP, NASDAQ: SHPGY), the global specialty
biopharmaceutical company, announces that a Luxembourg incorporated
wholly-owned subsidiary of Shire plc will launch a voluntary public
takeover offer for all the shares in Movetis NV, the Belgium-based European
specialty gastrointestinal (GI) company. Movetis is listed on Euronext and
focuses on discovering, developing and commercializing innovative
treatments for GI conditions with a high unmet medical need.

Movetis' board unanimously supports the transaction and will recommend
acceptance of the offer to its shareholders. Institutional shareholders
holding 38.9% of Movetis' issued share capital, have unconditionally agreed
to accept the offer in respect of their own shares.

This proposed acquisition will significantly broaden Shire's GI portfolio
and immediately add growing revenues, further expanding Shire's GI market
presence in Europe with the recently launched RESOLOR(R) (prucalopride), a
new chemical entity. RESOLOR is approved in the 27 countries of the European
Union as well as Iceland, Lichtenstein and Norway and is indicated for the
symptomatic treatment of chronic constipation in women in whom laxatives fail
to provide adequate relief. Movetis has the rights to RESOLOR in the EU,
Iceland, Lichtenstein, Norway and Switzerland and is entitled to royalties on
sales of RESOLOR outside of Europe from Johnson & Johnson.

Mike Cola, President of Shire's Specialty Pharmaceuticals business,
comments:

"This proposed acquisition of Movetis provides a highly complementary fit
for our GI business unit and supports our strategy of expanding our specialty
product portfolio into international markets. This is aligned with our
strategy of developing and commercializing medicines to address symptomatic
diseases treated by specialist physicians, in this case gastroenterologists.
The acquisition of Movetis will provide immediate revenue from a
newly-launched product that has strong patent protection, as well as a
promising GI pipeline."

Terms of the Offer

Shire will offer EUR19 per share in cash for all of the issued shares of
Movetis, valuing the company's fully diluted equity at EUR428 million (as at
March 31, 2010, their last reporting date, Movetis held EUR100 million in
cash; based on this the enterprise value (less cash) of Movetis would be
EUR328 million). The acquisition will be funded out of Shire's current cash
resources.

It is anticipated that the offer to Movetis' shareholders will open for
acceptance in September. The offer is contingent upon the fulfillment of
certain conditions, including receipt of acceptances in respect of at least
90% of the shares that are the subject of the offer and that Movetis does not
suffer a material adverse change before the results of the offer are
published.

Shire has entered into agreements with institutional shareholders in
which they have unconditionally committed 38.9% of Movetis' existing ordinary
share capital to the offer.

Once finalized, the prospectus will be published and circulated to
Movetis' shareholders, and details will be available on www.shire.com and
www.movetis.com. No action will be taken to permit a public tender offer in
any other jurisdiction than Belgium. This press release does not constitute
an invitation to sell or the solicitation of an offer to buy any security.

Deutsche Bank AG is acting as financial adviser to Shire.

Strategic Rationale for the Transaction

The acquisition adds to Shire's portfolio of treatments for GI conditions
with high unmet need and prescribed by specialist physicians. Shire's stated
strategic focus on GI led to the establishment several years ago of a
dedicated GI business unit. Shire's proposed acquisition of Movetis brings
rights to the recently approved RESOLOR in Europe as well as world-class
research and development talent and a promising GI pipeline, offering
additional opportunities for Shire. The acquisition will expand the growth of
Shire's marketed GI product portfolio internationally.

RESOLOR is a selective, high-affinity 5-HT(4) receptor agonist
specifically developed to target impaired motility associated with chronic
constipation. It has composition of matter patent protection extending
through 2020 and Shire estimates potential peak sales of over EUR300 million.
The patients in this category are generally served by specialist
gastroenterologists. Other marketed treatments for this condition are limited
or have associated serious adverse effects. In addition to RESOLOR, Movetis
has two projects in early clinical development and several pre-clinical leads
as well as the rights to a large library of qualified lead compounds with
potential for development and commercialization by Movetis in global markets
in different GI indications.

About Movetis

Movetis is a European specialty GI company that is focused on improving
the lives of millions of patients - both adults and children - by
discovering, developing and commercialising innovative treatments targeting
GI conditions with a high unmet medical need. Movetis NV was founded in
Belgium in November 2006 as a spin-off of Johnson & Johnson. Movetis has a
broad portfolio of GI products: Beside Resolor(R) (prucalopride), Movetis has
two products in Phase 2 development and two prioritised compounds in
preclinical development, all addressing important GI areas including ascites,
paediatric reflux, refractory GORD (gastroesophageal reflux disease) and
severe forms of irritable bowel syndrome. In addition, Movetis has rights to
a large library of qualified lead compounds with potential for development in
different GI indications and access to know how for compounds in secretory
diarrhoea. The current portfolio is licensed from Janssen Pharmaceutica NV,
Belgium and Ortho-McNeil Pharmaceutical Inc., two Johnson & Johnson
companies. Movetis shares are listed on Euronext Brussels under the ticker
MOVE.

About RESOLOR(R) (prucalopride)

RESOLOR (prucalopride) is a selective, high-affinity 5-HT4 receptor
agonist specifically developed to target impaired motility associated with
chronic constipation, thereby restoring normal bowel movement. Resolor
(prucalopride) is currently approved in thirty European countries (EU27,
Norway, Iceland and Lichtenstein) for the symptomatic treatment of chronic
constipation in women in whom laxatives fail to provide adequate relief. The
marketing authorisation application is currently under review in Switzerland.

About chronic constipation

Chronic constipation is characterised by infrequent and difficult passage
of stools over a prolonged period and a range of bothersome symptoms.
Traditional treatment options for chronic constipation consist mainly of
dietary and lifestyle changes in combination with laxatives.(i) However,
traditional therapies such as fibre or osmotic and stimulant laxatives do not
address the underlying cause(s) of chronic constipation(ii). This explains
why there is an important subgroup of patients who are not fully satisfied
with their current constipation relief therapy.(iii)

Notes to editors

SHIRE PLC

Shire's strategic goal is to become the leading specialty
biopharmaceutical company that focuses on meeting the needs of the specialist
physician. Shire focuses its business on attention deficit hyperactivity
disorder (ADHD), human genetic therapies (HGT) and gastrointestinal (GI)
diseases as well as opportunities in other therapeutic areas to the extent
they arise through acquisitions. Shire's in-licensing, merger and acquisition
efforts are focused on products in specialist markets with strong
intellectual property protection and global rights. Shire believes that a
carefully selected and balanced portfolio of products with strategically
aligned and relatively small-scale sales forces will deliver strong results.

For further information on Shire, please visit the Company's website:
www.shire.com.

"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, the Company's results could be
materially adversely affected. The risks and uncertainties include, but are
not limited to, risks associated with: the inherent uncertainty of research,
development, approval, reimbursement, manufacturing and commercialization of
the Company's Specialty Pharmaceutical and Human Genetic Therapies products,
as well as the ability to secure and integrate new products for
commercialization and/or development; government regulation of the Company's
products; the Company's ability to manufacture its products in sufficient
quantities to meet demand; the impact of competitive therapies on the
Company's products; the Company's ability to register, maintain and enforce
patents and other intellectual property rights relating to its products; the
Company's ability to obtain and maintain government and other third-party
reimbursement for its products; and other risks and uncertainties detailed
from time to time in the Company's filings with the Securities and Exchange
Commission.

DEUTSCHE BANK AG

Deutsche Bank AG is authorized under German Banking Law
(competent authority: BaFin - Federal Financial Supervisory Authority) and
authorized and subject to limited regulation by the FSA. Details about the
extent of Deutsche Bank AG's authorization and regulation by the FSA are
available on request.

    (i)   WGO Practice Guidelines - www.medscape.com/
    (ii)  Johanson Kralstein. Chronic constipation: a survey of the patient
          perspective. Aliment Pharmacol Ther 2007; 25:599-608
    (iii) Mertz H, Naliboff B, Mayer E. Physiology of refractory chronic
          constipation. Am J Gastroenterol 1999; 94:609-15.
    For further information please contact:

    Investor Relations:
    Eric Rojas, erojas@shire.com, +1-781-482-0999

    Media:
    Jessica Mann, jmann@shire.com, +44-1256-894-280
    Matthew Cabrey, mcabrey@shire.com, +1-484-595-8248

For further information please contact: Investor Relations: Eric Rojas, erojas at shire.com, +1-781-482-0999; Media: Jessica Mann, jmann at shire.com, +44-1256-894-280; Matthew Cabrey, mcabrey at shire.com, +1-484-595-8248

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