ng an up front
payment and success based clinical and sales milestones and excluding
royalties and cost sharing, Shire reimburses world-wide development costs
on a 50/50 basis, and in return Shire received rights to commercialize
these products outside of the U.S. while Amicus retains all rights to
commercialize these products in the U.S. In addition, Amicus leads
development operations through the end of Phase 2 clinical trials. The
companies then share responsibility for Phase 3 clinical trial development
leveraging Shire's significant ex-US regulatory and clinical experience as
well as its commercial infrastructure.
Additional Financial Results & Notes
On a reported basis, the net loss attributable to common stockholders
for the three months ended June 30, 2008, was $9.3 million as compared to
$9.7 million for the same period in 2007. On a non-GAAP basis, the net loss
for the three months ended June 30, 2008, was $7.4 million as compared to
$8.3 million in the same period in 2007.
Amicus recorded revenue during the second quarter of 2008 representing
two different revenue streams from the Shire agreement. Upon signing the
agreement, Amicus received an upfront payment of $50 million that will be
recognized as revenue on a straight-line basis over 18 years from the date
of the agreement. In the second quarter 2008, Amicus recognized $0.7
million of the Shire upfront payment and $3.1 million of research revenue
on reimbursed research and development costs.
Amicus today updated its previous guidance for 2008 cash burn of $40
million to $60 million to a new range of $40 million to $50 million. The
Company also stated that it does not expect to raise cash from any equity
financings in 2008.
The differences between U.S. GAAP and non U.S. GAAP financial results
are itemized in Tables 2 and 3, and are primarily due to:
-- Pre-tax stock compensation expense
-- Pre-tax charges for preferred stock accretion
-- P
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Page: 1 2 3 4 5 6 7 8 9 10 11 12 Related medicine technology :1.
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Amicus Therapeutics Announces Plans to Present Phase 1 Data for AT2220 for Pompe Disease7.
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