EPIX Pharmaceuticals Receives Response from the FDA Regarding Appeal of Vasovist(TM) Approvable Letters
28 August 2006 - 10:30PM
Business Wire
EPIX Pharmaceuticals, Inc. (NASDAQ: EPIXD) today announced that it
has received a letter from the U.S. Food and Drug Administration
(FDA) denying EPIX's formal appeal to approve its novel blood-pool
imaging agent Vasovist(TM) (gadofosveset trisodium) and turning
down EPIX's request for an Advisory Committee to review Vasovist.
In its response letter, the Office of New Drugs (OND) of the FDA
also suggested that if EPIX decides to conduct additional clinical
research to support approval, then rather than relying on a blinded
re-read of previously submitted data and data from a new clinical
trial, a safer course of action would be to conduct two new
clinical trials to support the application for approval. EPIX
submitted the appeal to the OND on June 30, 2006 in response to two
prior approvable letters for Vasovist. "We are disappointed by the
Agency's action. We are evaluating several options available to us
as next steps with Vasovist in the United States, including the
option to appeal this decision to the next level at the FDA, and
will update the market accordingly," said Andrew Uprichard, M.D.,
president of EPIX Pharmaceuticals. Dr. Uprichard added, "We remain
committed to bringing Vasovist to market in the United States.
Vasovist was approved throughout the European Union late last year
and is already being marketed in several countries within Europe.
Vasovist was also recently recommended for approval in Australia."
About Vasovist(TM) Vasovist is an injectable intravascular contrast
agent designed to provide visual imaging of the vascular system
through magnetic resonance angiography. EPIX's initial target
indication for Vasovist is for use in magnetic resonance
angiography imaging of non-coronary vascular disease. In October
2005, the European Medicines Agency granted marketing approval of
Vasovist for all 25 member states of the European Union. Vasovist
has also been approved in Switzerland and recommended for approval
in Australia. Vasovist has been studied in 18 clinical trials
totaling more than 1,400 patients. The clinical trials were
conducted to determine comparability of Vasovist MRA to
conventional catheter-based X-ray angiography for the
identification and characterization of vascular stenosis. The
studies included evaluation of a single bolus injection of Vasovist
for diagnosis of non-coronary vascular disease in the aortoiliac,
renal and pedal arteries. About EPIX EPIX Pharmaceuticals is a
biopharmaceutical company focused on discovering, developing and
commercializing novel pharmaceutical products through the use of
proprietary technology to better diagnose, treat and manage
patients. The company has a blood-pool imaging agent approved and
marketed in Europe (Vasovist(TM)), and five internally-discovered
drug candidates currently in clinical trials targeting conditions
such as anxiety, depression, Alzheimer's disease, cardiovascular
disease and obesity. These drug candidates include PRX-00023 in
Phase 3 clinical development for generalized anxiety disorder,
PRX-08066 in Phase 2 clinical development for pulmonary
hypertension associated with chronic obstructive pulmonary disease,
and PRX-03140, which has completed a Phase 1b clinical trial in
Alzheimer's patients. EPIX also has collaborations with leading
organizations, including Amgen, Cystic Fibrosis Foundation
Therapeutics, and Schering AG (Germany). For more information about
EPIX, please visit the company's website at www.epixpharma.com.
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