Abiomed raises revenue outlook, wins US
approval for heart pump
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[January 28, 2015]
(Reuters) - Medical device maker
Abiomed Inc <ABMD.O> raised its full-year revenue forecast and said the
U.S. Food and Drug Administration had approved its heart pump, sending
its stock up about 30 percent in extended trading.
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Abiomed's heart pump, Impella RP, helps blood circulation for up to
14 days in patients who develop acute right heart failure following
implantation, myocardial infarction, heart transplant or open-heart
surgery.
The device is the first percutaneous, single access pump approved
for right heart support, the company said.
In surgery, 'percutaneous' pertains to any procedure that allows
access to internal organs via a needle-puncture of the skin, rather
than by using an "open" approach where organs must be exposed,
typically using a scalpel.
The approval comes in the form of a humanitarian device exemption (HDE),
given for devices to treat rare conditions, affecting less than
4,000 people in the United States per year, and ones which have no
comparable products.
The decision comes about 6 weeks earlier than expected, and the
device will likely address upwards of 8,000 patients, Leerink Swann
analysts wrote in a note.
The FDA, on Tuesday, asked the company to conduct two post-approval
studies to evaluate Impella RP's safety and benefit profile.
Higher sales of other Impella devices helped Abiomed post
better-than-expected revenue for the third-quarter ending Dec. 31.
The company's revenue rose 34 percent to $62 million, well ahead of
analysts' average estimate of $53.2 million, according to Thomson
Reuters I/B/E/S.
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Abiomed also raised its revenue forecast for the year ending March
31 to $223-$226 million from $209-$212 million.
Analysts on average expect $211.4 million.
It hiked its operating margin estimate for the year to 9-11 percent
from 1-4 percent.
The company's stock closed at $38.63 on the Nasdaq on Tuesday.
(Reporting by Anjali Rao Koppala in Bengaluru; Editing by Ted Kerr
and Savio D'Souza)
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