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ABIOMED Presentations and Live Impella Cases to be Presented at Leading
Interventional Cardiology Meeting
Danvers, Mass., October 6, 2005—ABIOMED,
Inc. (NASDAQ: ABMD), a leading developer, manufacturer and marketer
of medical products designed to assist or replace the pumping function
of the failing heart, today announced its schedule of events at
the Cardiovascular Research Foundation’s (CRF) 17th Annual
Transcatheter Cardiovascular Therapeutics (TCT) scientific symposium,
being held in Washington, D.C. from October 16-21. ABIOMED will
be exhibiting at booth #254 from October 17-19 and will be featured
in numerous sessions throughout the meeting.
“The amount of interest we have received for ABIOMED and
Impella technology at this year’s upcoming TCT has been unprecedented
and recognizes the work we are doing to provide a robust family
of circulatory support devices that can recover the heart,”
said Michael R. Minogue, Chairman, CEO and President of ABIOMED.
“We are excited to provide interventional cardiologists with
information and demonstrations of the Impella Recover technology,
designed to deliver minimally invasive circulatory support in the
cath lab for such procedures as high risk angioplasty and stent
placement.”
Below is an outline of ABIOMED’s presence at TCT.
Monday, October 17
- 8:30 am—Tentative live left main insertion of Impella®
Recover® LP 2.5 by Dr. Eberhard Grube, Chief Cardiology/Angiology,
Heart Center, Siegburg, Germany (note: all live cases are subject
to change or cancellation).
- 3:30 pm—Oral Presentations, Room 147AB “Use of
the Impella Percutaneous Ventricular Unloading Catheter in High
Risk PCI,” Dr. Paolo Danna, Ospedale Luigi Sacco, Milan
Italy.
“Mechanical Circulatory Support Improves Recovery Outcomes
in Profound Cardiogenic Shock Post AMI,” Dr. Mark Anderson,
Associate Professor of Surgery and Chief Section of Cardiac
Surgery, Robert Wood Johnson University Hospital, New Brunswick,
New Jersey.
Tuesday, October 18
- 8:00 am—Tentative live Impella Case by Dr. Antonio Colombo
from San Raffaele Hospital in Milan, Italy. Shown in the main
arena (note: all live cases are subject to change or cancellation).
- 10:00 am or 11:30 am—Tentative live Impella Case in Masters
Auditorium or Coronary Theater by Dr. Eulogio Garcia from Madrid,
Spain (note: all live cases are subject to change or cancellation)
- 5:15 pm—Plenary Session II, Main Arena “Hemodynamic
Support Can Save Lives: The Optimal Device-Based Approach in Patients
with End-Stage CHF,” Dr. Donald Baim, Professor of Medicine,
Harvard Medical School; Director, Center for Integration of Medicine
and Innovative Technology, Brigham and Women’s Hospital,
Boston.
- 7:00 pm—ABIOMED Co-Sponsored Event “Accelerating
Device Based Therapy for Heart Failure and Recovery” with
Keynote address by Dr. Martin Leon at the Renaissance Hotel, Ballroom.
Presentations include: “The Future Role of Percutaneous
Ventricular Assist Catheters in Interventional Cardiology”
by Dr. Eberhard Grube; “Bridge to Recovery: Experience with
ABIOMED Ventricular Assist Devices,” by Dr. Mark Anderson.
Wednesday, October 19
- 6:22 pm—Case Review Session, Room 149AB “Novel Hemodynamic
Support During High Risk Coronary Anatomy,” Dr. J.P. Simao
Henriques, Academic Medical Center, Amsterdam, Netherlands.
Thursday, October 20
- 2:40 pm—Oral Presentation, Room 150AB “LV Support
Device Impella Increase Coronary Blood Flow in Patients with Compromised
LV Undergoing Angioplasty,” Dr. Maurice Remmelink, Academic
Medical Center, Amsterdam, Netherlands.
ABOUT TRANSCATHETER CARDIOVASCULAR THERAPEUTICS 2005
Transcatheter Cardiovascular Therapeutics (TCT), sponsored by the
Cardiovascular Research Foundation(R), is a scientifically stimulating
symposium for physicians and other health care professionals who
specialize in the field of interventional vascular therapy. This
year's event is scheduled for Oct. 16-21, 2005, Washington Convention
Center, Washington, D.C. For more information, please visit
http://www.tct2005.com.
ABOUT ABIOMED
Based in Danvers, Massachusetts, ABIOMED, Inc. (pronounced “AB’-EE-O-MED”)
is a leading developer, manufacturer and marketer of medical products
designed to assist or replace the pumping function of the failing
heart. ABIOMED currently manufactures and sells the AB5000™
Circulatory Support System and the BVS® 5000 Biventricular Support
System for the temporary support of all patients with failing but
potentially recoverable hearts. In Europe, ABIOMED offers the Impella®
Recover™ minimally invasive cardiovascular support systems
under CE Mark approval. The Company’s AbioCor® Implantable
Replacement Heart was the subject of an initial clinical trial under
an Investigational Device Exemption from the United States Food
and Drug Administration. The AbioCor has not been approved for commercial
distribution, and is not available for use or sale outside of the
initial clinical trial. For additional information please visit:
www.abiomed.com.
IMPELLA DEVICES
Impella products are investigational devices limited by Federal
Law solely to investigational use in the United States and are not
yet available for sale in the United States
Contacts:
Liza Heapes
ABIOMED INC.
Media Relations
(978) 646-1668
mediarelations@abiomed.com
Investor Relations Contact:
Melody Carey
Rx COmmunications Group, LLC
(917) 322-2571
mcarey@rxir.com
FORWARD-LOOKING STATEMENTS
This Release contains forward-looking statements, including statements
regarding development of ABIOMED’s existing and new products,
the Company’s progress toward commercial growth, and future
opportunities. The Company’s actual results may differ materially
from those anticipated in these forward-looking statements based
upon a number of factors, including uncertainties associated with
development, testing and related regulatory approvals, anticipated
future losses, complex manufacturing, high quality requirements,
dependence on limited sources of supply, competition, technological
change, government regulation, future capital needs and uncertainty
of additional financing and other risks and challenges detailed
in the Company’s filings with the Securities and Exchange
Commission, including the Annual Report filed on Form 10-K. Readers
are cautioned not to place undue reliance on any forward-looking
statements, which speak only as of the date of this Release. The
Company undertakes no obligation to publicly release the results
of any revisions to these forward-looking statements that may be
made to reflect events or circumstances that occur after the date
of this Release or to reflect the occurrence of unanticipated events.
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