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Memory Pharmaceuticals & Roche Expand Development Program For MEM 3454 In Schizophrenia
Memory 
Pharmaceuticals Corp. (Nasdaq: MEMY) announced that it plans to 
conduct a clinical study of MEM 3454, the Company's lead nicotinic alpha-7 
partial agonist, on two biomarkers of schizophrenia, P50 sensory gating and 
mismatch negativity, in patients with schizophrenia. The biomarker study, 
and additional formulation and manufacturing activities for MEM 3454, will 
be funded by Roche, under the companies' collaboration for the development 
of nicotinic alpha-7 receptor agonists.
 
    
"This new study will greatly enhance our ability to measure and predict 
the efficacy of MEM 3454 and other compounds in the nicotinic alpha-7 
receptor program," said Stephen Murray, MD, Ph.D, Chief Medical Officer of 
Memory Pharmaceuticals Corp. "The study should be underway this summer with 
data available by early 2009. The biomarker data, together with the results 
of our ongoing Phase 2a study in CIAS, will help with the design of 
later-stage trials in schizophrenia."
 
    
The biomarker study will enroll approximately 12 patients with stable 
schizophrenia who are receiving atypical antipsychotic therapy. Subjects 
will be randomized to receive MEM 3454 and placebo in a 5-way cross-over 
design. Each subject will participate in 5 treatment periods. During each 
period, subjects will receive single doses of 1 mg, 5 mg, 15 mg, or 50 mg 
of MEM 3454 or placebo, with a 4-day wash-out period between each treatment 
period. The primary objective of the trial is to study P50 sensory gating 
and mismatch negativity as potential efficacy biomarkers for nicotinic 
alpha-7 agonists, such as MEM 3454, in schizophrenia. P50 sensory gating 
and mismatch negativity are two neurophysiological measurements that have 
been shown to be closely associated with nicotinic alpha-7 function and 
schizophrenia.
 
    
In November 2007, Memory Pharmaceuticals announced positive Phase 2a 
data from a clinical trial of MEM 3454 in Alzheimer's disease. MEM 3454 
demonstrated a statistically significant effect on cognition at the 5 mg 
and 15 mg doses on both the primary and key secondary endpoints for that 
trial. Roche has an option to a worldwide, exclusive license to develop and 
commercialize MEM 3454 upon the delivery by Memory of the study report of 
the Phase 2a AD study and the fulfillment of certain additional predefined 
events. Roche is obligated to make a milestone payment to Memory 
Pharmaceuticals at the time this option is exercised.
 
    
In December 2007, as part of the development program for MEM 3454 in 
schizophrenia, Memory Pharmaceuticals commenced a Phase 2a clinical trial 
of MEM 3454 in CIAS. To maintain its license to MEM 3454, Roche would have 
to make an additional milestone payment to the Company upon completion of 
the ongoing Phase 2a CIAS trial, which is expected to be completed in the 
fourth quarter of 2008.
 
    
Evoked Potentials in Schizophrenia
    
Electrophysiology measures have long been used to detect changes in 
brain activity in patients with schizophrenia. These patients often have a 
diminished ability to suppress the evoked response to the second of two 
auditory stimuli, which is known as sensory gating. A number of both 
preclinical and clinical studies have shown that this abnormality is 
genetically linked to the nicotinic alpha-7 receptor and can be measured 
through the P50 auditory evoked response, a positive waveform measured 50 
milliseconds after an auditory stimulus. Recent scientific studies have 
shown that a nicotinic alpha-7 agonist can both improve cognition and 
improve P50 inhibition, giving rise to the possibility that P50 can be used 
to track cognitive effects for this class of compounds. Another auditory 
electrophysiology evoked potential measure that is abnormal in patients 
with schizophrenia is mismatched negativity, which is the ability to detect 
a deviation from a repetitive auditory pattern. Both of these evoked 
potential abnormalities in schizophrenia have been shown to be reversed by 
treatment.
 
    
About MEM 3454
    
MEM 3454 is a partial agonist of the nicotinic alpha-7 receptor, a 
highly specialized receptor found in the central nervous system. Compounds 
acting on this receptor could be beneficial in the treatment of Alzheimer's 
disease and schizophrenia, as well as other psychiatric and neurological 
disorders. MEM 3454 is being developed by Memory Pharmaceuticals under its 
Strategic Alliance Agreement with Roche for the development of nicotinic 
alpha-7 receptor agonists and is the Company's lead drug candidate from its 
nicotinic alpha-7 agonist program.
 
    
About the Company
    
Memory Pharmaceuticals Corp., a biopharmaceutical company, is focused 
on developing innovative drugs for the treatment of debilitating CNS 
disorders such as Alzheimer's disease, schizophrenia and depression. For 
additional information, please visit our website at 
http://www.memorypharma.com.
 
    
Safe Harbor Statement
    
This press release contains forward-looking statements within the  
meaning of the Private Securities Litigation Reform Act of 1995 that are 
subject to risks and uncertainties. All statements, other than statements 
of historical facts, regarding management's expectations, beliefs, goals, 
plans or Memory Pharmaceuticals' prospects, future financial position, 
future revenues and projected costs should be considered forward-looking. 
Readers are cautioned that actual results may differ materially from 
projections or estimates due to a variety of important factors, including 
the risks and uncertainties associated with: obtaining additional financing 
to support Memory Pharmaceuticals' R&D and clinical activities and 
operations; the outcome of clinical trials of Memory Pharmaceuticals' drug 
candidates and whether they demonstrate these candidates' safety and 
effectiveness; obtaining regulatory approvals to conduct clinical trials 
and to commercialize Memory Pharmaceuticals' drug candidates; Memory 
Pharmaceuticals' ability to enter into and maintain collaborations with 
third parties for its drug development programs; Memory Pharmaceuticals' 
dependence on its collaborations and its license relationships; achieving 
milestones under Memory Pharmaceuticals' collaborations; Memory 
Pharmaceuticals' dependence on preclinical and clinical investigators, 
preclinical and clinical research organizations, manufacturers and 
consultants; and protecting the intellectual property developed by or 
licensed to Memory Pharmaceuticals. These and other risks are described in 
greater detail in Memory Pharmaceuticals' filings with the Securities and 
Exchange Commission. Memory Pharmaceuticals may not actually achieve the 
goals or plans described in its forward-looking statements, and investors 
should not place undue reliance on these statements. Memory Pharmaceuticals  
disclaims any intent or obligation to update any forward-looking statements 
as a result of developments occurring after the date of this press release.
 
Memory Pharmaceuticals Corp.
http://www.memorypharma.com
		
Memorie de produse farmaceutice Roche & expandare program de dezvoltare pentru 3454 mem în schizofrenie - Memory Pharmaceuticals & Roche Expand Development Program For MEM 3454 In Schizophrenia - articole medicale engleza - startsanatate