�Neurobiological  
Technologies,  Inc.  (NTI(R))  (Nasdaq:  NTII)  announced that enrollment 
into its deuce Phase  3 pivotal studies evaluating Viprinex(TM)  (ancrod) for 
the discussion of acute ischemic stroke has reached the layer of patients            
necessary to conduct a planned interim analysis crosswise the two studies. NTI  
is presently studying whether Viprinex  is safe and effective for treating 
acute ischemic stroke when given within six-spot hours of stroke onset.
    
"We  ar very pleased to experience reached the enrollment criteria to lead         
the aforethought interim analysis," stated Paul  E.  Freiman,  president and chief 
executive officer of NTI.  "Our  independent Data  Safety  Monitoring  Board          
(DSMB)  will meet to limited review the efficaciousness data on an unblinded basis for the 
first time. In  addition, the DSMB  volition evaluate the safety of Viprinex,  as 
they've been doing since the startle of the studies."
    
Results  of the interim analysis are expected in January  2009. The         
interim analysis will be based on the first 500 tempered patients in the               
stream trials wHO have completed their 90 day judgment. If  the treatment 
effect observed for the ancrod patients is not bettor than that observed 
for the placebo patients, then the trials will be halted for futility,              
indicating that they are unlikely to attest the benefit required for 
approval. If  the trials are allowed to continue, NTI  testament not experience access 
to any unblinded patient information until the trials ar completed. The  primary 
termination of the trials is the modified Rankin  Score,  a quantity of 
disablement.
    
"We  believe that data from five hundred patients is sufficient for the DSMB  to  
comport a thorough assessment of futility, and have consequently moved up 
the meantime analysis from earlier plans to conduct it at 650 patients," 
stated Warren  W.  Wasiewski,  M.D.,  vice president and chief medical officer. 
"This  is a significant milestone for the program and we are all look 
forward to learning the outcome of this review."
About  Ischemic  Stroke
     
Ischemic  accident is caused by obstruction of a blood vessel in the brain 
referable to a clot. The  lack of blood flow, or ischemia, leads to cell death. 
According  to the American  Heart  Association,  87% of the 700,000 yearly 
strokes in the United  States  are ischemic. Stroke  is the third preeminent 
cause of death in the United  States,  behind heart disease and cancer, and 
the leading cause of handicap. The  only FDA-approved  do drugs for the 
treatment of acute ischemic stroke is Activase(R)  (alteplase), which 
presently must be given within three hours of stroke onset.
About  Neurobiological  Technologies,  Inc.
     
Neurobiological  Technologies,  Inc.,  (Nasdaq:  NTII)  is a 
biopharmaceutical company focussed on developing novel, first-in-class 
agents for central nervous system atmospheric condition and former serious unmet 
medical necessarily. The  Company's  most advanced product campaigner, Viprinex(TM)  
(ancrod), is in Phase  3 clinical testing as a novel investigational drug 
for the treatment of acute ischemic cerebrovascular accident. Viprinex  has multiple 
mechanisms of action and is specifically designed to double the time period 
that patients can buoy be treated after the onset of a stroke. Acute  ischaemic 
stroke is one of the about prevalent, debilitating and pricy diseases in 
the humans for which there are few satisfactory treatment options. NTI  too 
has early-stage development programs for Alzheimer's  and Huntington's  
diseases and rights to receive payments on an approved dose for Alzheimer's  
disease and an investigational drug in Phase  3 trials for brain swelling.
Forward  Looking  Statements
     
Except  for the historical information contained herein, the matters 
discussed in this press release are modern statements that involve 
risks and uncertainties, including uncertainties regarding the outcome of 
the interim analysis, obtaining approval for Viprinex,  levels of future 
expenditures and capital resources needed to fund trading operations, as well as 
other risks elaborated from sentence to time in our filings with the Securities  
and Exchange  Commission,  including our Annual  Report  on Form  10-K  as  
updated periodically in Quarterly  Reports  on Form  10-Q  and Current  Reports  
on Form  8-K.  Actual  results whitethorn differ materially from those projected. 
These  forward-looking statements represent our judgment as of the date of 
the release and we undertake no obligation to update these forward-looking 
statements.
 
Neurobiological  Technologies,  Inc.
http://www.ntii.com
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