Alteon Initiates 'SPECTRA,' Trial of Alagebrium Chloride (ALT-711) In Patients With Systolic Hypertension

Alteon Initiates 'SPECTRA,' Trial of Alagebrium Chloride (ALT-711) In Patients
With Systolic Hypertension
- First in New Class of Drugs to Target Underlying Cause of Systolic
Hypertension, Most Common Form of High Blood Pressure in People Over 50, and
Type Least Likely to Be Well Treated - 


PARSIPPANY, N.J., March 10  /PRNewswire-FirstCall/ -- Alteon Inc. announced
today that it has initiated a Phase 2b clinical trial of Alteon's lead A.G.E.
Crosslink Breaker, alagebrium chloride, in patients with systolic hypertension. 
SPECTRA (Systolic Pressure Efficacy and Safety Trial of Alagebrium) is designed
to evaluate alagebrium's ability to lower systolic blood pressure in patients
with a systolic blood pressure reading of greater than or equal to 140 mm Hg (by
ambulatory blood pressure measurements), building upon positive data from
previous Phase 2 trials.  Alagebrium's activity in prior clinical trials
demonstrated the drug's safety and ability to lower systolic blood pressure and
pulse pressure inaging patients, especially in a difficult-to-treat
hypertensive patient population.  Notably, alagebrium's beneficial effect was
demonstrated over and above standard treatments, and data thus far point to a
mechanism of action unlike any existing bloodpressure agent.

Systolic hypertension is the most common form of hypertension in people over age
50, and recent statistics estimate its prevalence at more than 20 million
individuals in the U.S. alone.  The condition is defined as an elevated systolic
pressure (the top number in a blood pressure reading) of 140 mm Hg or higher. 
Systolic hypertension is also characterized by an increased pulse pressure, the
difference between the systolic and diastolic (the bottom number in a blood
pressure reading)blood pressures, a marker for vascular stiffness.  The
prevalence of systolic hypertension increases with age, with systolic
hypertension becoming far more common than diastolic hypertension.  Yet, it is
the type of hypertension least likely to be well-treated, according to the
American Heart Association, in part due to the fact that current blood pressure
drugs do not specifically target systolic hypertension.  Current treatment
options are therefore limited.

Alagebrium is the most clinically advanced drug in a new class of compounds
known as Advanced Glycation End-product (A.G.E.) Crosslink Breakers, which were
discovered by Alteon.  By "breaking" the pathological bonds that cause tissues,
organs and vessels to stiffen and lose function over time, alagebrium has
demonstrated the ability to reverse certain age-related and diabetes-related
conditions.  In previous Phase 2 testing in cardiovascular disease, treatment
with alagebrium resulted in statistically significant and clinically meaningful
effects of increasing vascular wall elasticity and lowering pulse pressure.  In
a post hoc analysis of a recent Phase 2 trial, alagebrium treatment resulted in
significant lowering of systolic blood pressures in patients (as measured by
ambulatory bloodpressure measurements) with baseline systolic pressures of 140
mm Hg or greater whose condition was uncontrolled despite treatment with one or
more currently available blood pressure medications.  SPECTRA will further
evaluate alagebrium's activity in these patients, who represent a major unmet
medical need.

"Initiation of SPECTRA is a key milestone in our program for the development of
alagebrium in cardiovascular disease.  We are enthusiastic about the potential
that alagebrium has demonstrated insystolic hypertension and we are
aggressively pursuing clinical development in this indication," said Robert C.
deGroof, Senior Vice President, Scientific Affairs.

About SPECTRA

In the SPECTRA trial, alagebrium will be tested in approximately 390 patients at
over 50 clinical sites throughout the United States.  The trial will include
male and female patients at least 45 years of age.  Recruited patients will
undergo a wash-out period, when they are weaned from their existing
antihypertensive treatment, followed by a run-in phase during which they will be
stabilized on a diuretic.  They will then receive alagebrium tablets or placebo
once a day for 12 weeks.

SPECTRA will further extend the range of effective dosing defined in previous
Phase 2 testing.  The study will consist of four treatment arms, comprising
three different dose levels of alagebrium (10, 50 or 150 mg) or placebo. 
Patients enrolled in the trial must have systolic blood pressure of greater or
equal to 140 mm Hg as measured by ambulatory blood pressure monitoring (ABPM),
as well as additional qualifications.  Automated office blood pressures
(oscillometric) as well as ABPM pressures will be taken at scheduled time
points.  Change from baseline in mean 24-hour systolic ABPM pressure after 12
weeks of dosing (as compared to placebo) will be evaluated as the primary
measure of efficacy.  Secondary endpoints will include changes in diastolic,
pulse and arterial pressures.

A.G.E. Crosslink Breakers and Alagebrium

Advanced Glycation End-products (A.G.E.s) are permanent glucose structures that
form when glucose binds to the surface of proteins.  Many of these proteins,
including structural proteins such as collagen and elastin, play an integral
role in the maintenance of cardiovascular elasticity function and vascular wall
integrity.  This process can impair the normal function of organs that depend on
flexibility for normal function, such as blood vessels and cardiac muscle. 
Alagebrium is the first in the A.G.E. Crosslink Breaker class that has been
shown to reverse or "break" A.G.E. crosslinks, thereby restoring more normal
function to organs and tissues that have lost flexibility.  Pharmacologic
intervention with alagebrium directly targets the biochemical pathway leading to
the stiffness of the cardiovascular system. Its mechanism of action is new and
novel, and is unrelated to that of any pharmaceutical agent either currently
prescribed or in clinical development. Importantly, alagebrium does not disrupt
the naturalenzymatic glycation sites or peptide bonds that are responsible for
maintaining the normal integrity of the collagen chain.  Thus, normal structure
and function is preserved while abnormal crosslinking is reduced.

About Alteon

Alteon is developing several new classes of drugs that reverse or slow down
diseases of aging and complications of diabetes.  These compounds have an impact
on a fundamental pathological process caused by protein-glucose complexes called
Advanced Glycation End-products (A.G.E.s).  The formation and crosslinking of
A.G.E.s lead to a loss of flexibility and function in body tissues, organs and
vessels and have been shown to be a causative factor in many age-related
diseases and diabetic complications.  Alteon has created a library of novel
classes of compounds targeting the A.G.E. Pathway.  These include A.G.E.
Crosslink Breakers, A.G.E. Formation Inhibitors and Glucose Lowering Agents. 
Alteon's lead compound alagebrium chloride (formerly ALT-711), the only A.G.E.
Crosslink Breaker in advanced human testing, has demonstrated safety and
efficacy in several Phase 2 trials and is actively being developed for systolic
hypertension and heart failure.  For more information on Alteon, visit the
company's website at http://www.alteon.com/.

Any statements contained in this press release that relate to future plans,
events or performance are forward-looking statements that involve risks and
uncertainties including, but not limited to, those relating to technology and
product development (including the possibility that early clinical trial results
may not be predictive of results that will be obtained in large-scale testing or
that any clinical trials will not demonstrate sufficient safety and efficacy to
obtain requisite approvals or will not result in marketable products),
regulatory approval processes, intellectual property rights and litigation,
competitive products, ability to obtain financing, and other risks identified in
Alteon's filings with the Securities and Exchange Commission. The information
contained in this press release is accurate as of the date indicated.  Actual
results, events or performance may differ materially. Alteon undertakes no
obligation to publicly release the result of any revision to these
forward-looking statements that may be made to reflect events or circumstances
after the date hereof or to reflect the occurrence of unanticipated events. 

DATASOURCE: Alteon Inc.



CONTACT:  Susan M. Pietropaolo, Director, Corporate Communications &

Investor Relations of Alteon Inc., [phone], fax - [phone]



Web site:  http://www.alteonpharma.com/ 

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