NEW YORK, May 31 /PRNewswire-FirstCall/ -- Forest Laboratories, Inc.
(NYSE: FRX) and PAION AG (Aachen, Germany -- Frankfurt Stock Exchange,
Prime Standard: PA8) today announced topline results of the DIAS-2
(Desmoteplase In Acute Ischemic Stroke) study with the compound
Desmoteplase. The Phase III study was designed to investigate the
improvement of clinical outcome in patients with acute ischemic stroke
treated with Desmoteplase within 3 to 9 hours after onset of stroke
symptoms as compared to placebo. The primary efficacy endpoint (difference
between active treatment and placebo in percentage of composite responders
as defined below) was not met. The blinded, randomized, placebo-controlled,
dose-ranging trial was jointly conducted by PAION and Forest Laboratories,
Inc., and enrolled a total of 186 patients in Europe, USA, Canada,
Australia, Hong Kong and Singapore. Forest Laboratories, Inc. is the
partner of PAION for Desmoteplase for North America and H. Lundbeck A/S is
PAION's partner for the rest of the world.
(Logo: http://www.newscom.com/cgi-bin/prnh/20001011/FORESTLOGO )
In this study, patients received either placebo (N=63), 90 mcg/kg
(N=57), or 125 mcg/kg (N=66) of Desmoteplase as an intravenous bolus within
3-9 hours after the onset of stroke. Patients were eligible for treatment
only in case of a distinct penumbra of at least 20% (insufficiently
perfused but still salvageable tissue area around the primary location of
stroke), which was confirmed by magnetic resonance imaging (MRI) or
perfusion computed tomography (pCT).
The primary efficacy endpoint in the study was clinical improvement at
Day 90 defined for each patient as achievement of all three of the
following criteria; (1): Improvement of greater than or equal to 8 points
from baseline on the National Institutes of Health Stroke Scale (NIHSS) or
NIHSS score less than or equal to 1, (2): Modified Rankin Scale (MRS) score
of 0-2, and (3): Barthel Index (BI) score of 75-100. Only patients who
simultaneously met the criteria along all three scales were considered
responders. Patients defined as responders by such criteria are in general
able to function independently, having no or few deficits.
Improvement of clinical outcome was found with 47.4% of patients
treated with 90 mcg/kg Desmoteplase and 36.4% of patients treated with 125
mcg/kg Desmoteplase, compared to 46.0% in the placebo group with neither
dose of Desmoteplase statistically significantly different compared to
placebo.
The rate of symptomatic intracranial bleeding within 72 hours after
study drug administration was 0% in the placebo group, 3.5% in the 90
mcg/kg dose group and 4.5% in the 125 mcg/kg group. There were four patient
deaths reported in the placebo group, three reported in the 90 mcg/kg dose
group and 14 reported in the 125 mcg/kg dose group within the 90 day
follow-up period. Ten of the 14 deaths in the 125 mcg/kg dose group were
considered by the investigators as not related to the drug, 9 of which
occurred 14 or more days after stroke and were from non-neurological
causes.
These data are surprising and are not consistent with previously
observed patterns in the DIAS/DEDAS trials and larger size,
placebo-controlled acute stroke trials. The absence of consistency with
previous findings is not easy to explain, but in-depth analyses are planned
to better understand the data.
Forest will review the complete study database over the coming weeks to
determine the appropriate next steps and its role regarding U.S.
development of desmoteplase.
The headline results of the DIAS-2 study will be presented on 1 June
2007 at 10:45 a.m. BST within the "Large Clinical Trials II" session at the
XVI European Stroke Conference in Glasgow, Scotland, U.K.
PAION will host a conference call on 1 June 2007 to discuss the DIAS-2
headline results starting at 1:00 p.m. BST (02:00 p.m. CEST, 08:00 a.m.
EDT). To access the call please dial +44 20 7138 0819 UK, +49 69 9897 2634
Germany, +1 718 354 1361 USA. Title: "PAION DIAS-2 results"
A replay of the call will be available until end of June 5, 2007, at
+44 20 7806 1970 UK, +49 69 22222 0418 Germany, +1 718 354 1112 USA, Replay
Passcode: 4318989#
In addition, a webcast of the conference call (listen-only mode) will
be accessible through a link provided on PAION's corporate website at
http://www.paion.de.
About Desmoteplase
Desmoteplase, the most fibrin-specific plasminogen activator known
today, is a genetically engineered clot-dissolving protein found in the
saliva of the vampire bat Desmodus rotundus. It has received fast-track
designation from the U.S. Food and Drug Administration for the indication
of acute ischemic stroke.
About Stroke
According to a recent publication by the American Stroke Association
(ASA), stroke now is the second leading cause of death worldwide and is a
leading cause of serious, long-term disability. In the U.S. alone, 700,000
people suffer a stroke each year, and approximately 20% die within four
weeks. For the U.S., the American Heart Association (AHA) expects the
financial burden of stroke due to in-hospital costs, long-term care
programs and productivity losses to be 63 billion dollars in 2007 alone.
About Forest Laboratories and Its Products
Forest Laboratories (http://www.frx.com) is a U.S.-based pharmaceutical
company dedicated to identifying, developing and delivering products that
make a positive difference in peoples' lives. Forest Laboratories' growing
product line includes Lexapro(R) (escitalopram oxalate), an SSRI indicated
for adults for the initial and maintenance treatment of major depressive
disorder and generalized anxiety disorder; Namenda(R) (memantine HCl), an
N-methyl D- aspartate (NMDA)-receptor antagonist indicated for the
treatment of moderate to severe Alzheimer's disease; Benicar(R)*
(olmesartan medoxomil), an angiotensin receptor blocker, and Benicar*
HCT(R) (olmesartan medoxomil- hydrochlorothiazide), an angiotensin receptor
blocker and diuretic combination product, each indicated for the treatment
of hypertension; and Campral(R)* (acamprosate calcium), indicated in
combination with psychosocial support for the maintenance of abstinence
from alcohol in patients with alcohol dependence who are abstinent at
treatment initiation.
*Benicar is a registered trademark of Daiichi Sankyo, Inc., and Campral
is a registered trademark of Merck Sante s.a.s., subsidiary of Merck KGaA,
Darmstadt, Germany.
Except for the historical information contained herein, this release
contains "forward-looking statements" within the meaning of the Private
Securities Litigation Reform Act of 1995. These statements involve a number
of risks and uncertainties, including the difficulty of predicting FDA
approvals, the acceptance and demand for new pharmaceutical products, the
impact of competitive products and pricing, the timely development and
launch of new products, and the risk factors listed from time to time in
the Forest Laboratories' SEC reports, including the Company's Annual Report
on Form 10-K for the fiscal year ended March 31, 2007.
SOURCE Forest Laboratories, Inc.
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Related links:
http://www.frx.com/
Photo Notes:
NewsCom: http://www.newscom.com/cgi-bin/prnh/20001011/FORESTLOGO
AP Archive: http://photoarchive.ap.org
PRN Photo Desk, photodesk@prnewswire.com
CONTACT:
Charles E. Triano, Vice President - Investor
Relations of Forest Laboratories, Inc., +1-212-224-6714,
Charles.Triano@frx.com
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