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NeoTherapeutics Completes Site Selection for Neotrofin(TM) Phase 2
Parkinson's Disease Trial


Patient enrollment accelerating with expanded program

IRVINE, Calif., Aug. 23 /PRNewswire/ -- NeoTherapeutics, Inc. (Nasdaq: <A
HREF="aol://4785:NEOT">NEOT</A>; NEOTW) announced today that it has expanded
its Neotrofin phase 2 Parkinson's disease trial to include four additional
clinical locations. New participants include Memorial Hospital of Rhode
Island (Providence), Rush Presbyterian-St. Luke's Medical Center (Chicago),
The Parkinson's Institute (Sunnyvale, CA), and Oregon Health & Science
University (Portland). Ten patients are currently receiving either Neotrofin
or placebo, including seven patients at the Parkinson's and Movement Disorder
Institute at Long Beach Memorial Hospital.

"With site selection completed, we can now focus on enrolling the additional
patients necessary to complete this clinical study," said F. Jacob Huff,
M.D., Vice President, Medical Affairs of NeoTherapeutics. "We are fortunate
to be working with some of the leading experts in the country in the
treatment of Parkinson's disease, and we expect to gain insights into safety
and dosing in Parkinson's patients from this study."

"Neotrofin uses the body's own tools to protect, repair and rebuild nerves in
the brain," stated Rajesh C. Shrotriya, M.D., President and Chief Operating
Officer of NeoTherapeutics.  "Our drug activates nerve growth factors, which
in addition to helping repair nerves, cause the proliferation of stem cells
that already exist in the brain. Additional growth factors stimulated by
Neotrofin may then cause the differentiation and maturation of these new stem
cells into new neurons, which could repair the damage done by
neurodegenerative conditions such as Parkinson's disease."

Patients participating in this trial will receive doses of Neotrofin
escalating from 250 mg to 1,000 mg twice per day for twelve weeks. In
addition to extensive assessments of tolerance and safety, the Unified
Parkinson's Disease Rating Scale (UPDRS)-part III (Motor Scale) will be used
as the primary measure of preliminary efficacy. Several other Parkinson's
disease rating scales will be used as secondary efficacy measures.

Parkinson's disease is one of the major neurodegenerative disorders affecting
more than one million patients in North America alone. The principal
hallmarks of Parkinson's disease are slowness of movement, rigidity and
tremor. Although current treatments provide some symptomatic relief,
Parkinson's disease progresses inexorably, often over 10 to 20 years, to
severe immobility and a bedridden state.

NeoTherapeutics seeks to create value for stockholders through the
development of central nervous system drugs by its neurology division, in-
licensing and development of anti-cancer drugs through its NeoOncoRx
subsidiary, and the licensing out of new drug targets through its NeoGene
Technologies subsidiary. The Company's most advanced drug, Neotrofin(TM), is
currently being developed for Alzheimer's disease and other neurodegenerative
diseases, such as Parkinson's disease and spinal cord injury. For additional
information visit the Company's web site at www.neotherapeutics.com.

This press release may contain forward-looking statements regarding future
events and the future performance of NeoTherapeutics that involve risks and
uncertainties that could cause actual results to differ materially.  These
risks are described in further detail in the Company's reports filed with the
Securities and Exchange Commission.

Contacts:

MEDIA RELATIONS

Jon Siegal

Ronald Trahan Associates (RTA) Inc.

(508) 647-9782, ext. 15

INVESTOR RELATIONS

John McManus

NeoTherapeutics, Inc.

(949) 788-6700, ext. 247

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SOURCE  NeoTherapeutics, Inc.

CO:  NeoTherapeutics, Inc.

ST:  California

IN:  MTC

SU:

08/23/2001 09:15 EDT http://www.prnewswire.com

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