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Lpath Demonstrates Preclinical Efficacy Of Lpathomab(TM) And Initiates Humanization Process
Lpath, Inc. (OTC Bulletin 
Board: LPTN), the category leader in therapeutic agents against bioactive 
lipids, reported positive results in several murine models of human cancer 
and AMD with Lpathomab(TM), the company's mouse monoclonal antibody against  
LPA (lysophosphatidic acid). These results confirm the expected potent 
anti angiogenic and anti metastatic actions of Lpathomab. Lpathomab was 
created using Lpath's proprietary ImmuneY2(TM) platform technology.
  
Based on this positive outcome, Lpath will collaborate with DataMabs of 
London, England, to humanize Lpathomab to create a lead antibody for pre  
clinical development.
 
    
LPA is a bioactive lipid long recognized as a significant promoter of 
cancer cell growth and metastasis in a broad range of tumor types, as well 
as a significant contributor to neuropathic pain.
 
    
"Humanizing our Lpathomab antibody is a vital next step in moving the 
project into the clinic," said Genevieve Hansen, Ph.D., Lpath's vice 
president of research. "We've had great success in the past working with 
DataMabs and look forward to working with them again on our Lpathomab   
project."
 
    
This achievement with Lpathomab comes on the heels of Lpath's success 
with its Sphingomab(TM) program. Sphingomab is an antibody against another  
bioactive lipid, S1P. Lpath humanized the antibody in 2006 and plans to 
file an IND in November of this year for the use of ASONEP(TM) (the 
systemic formulation of humanized Sphingomab) for the treatment of cancer. 
It also plans to file a second IND early next year for the use of 
iSONEP(TM) (the ocular formulation of humanized Sphingomab) for the 
treatment of AMD. The company plans to submit an IND filing for the use of 
humanized Lpathomab in 2009.
 
    
Dr. Roger Sabbadini, the founder and CSO of Lpath, commented, "These 
exciting results provide further validation of lipidomic-based therapeutics 
as an important new area of drug discovery. Lpath was one of the first 
companies to recognize that bioactive-lipid-signaling molecules, like S1P 
and LPA, could be excellent targets for rational drug design. By pursuing 
these targets and demonstrating compelling efficacy, we've opened up an 
entire class of lipidomic-based therapeutics for the treatment of cancer, 
diabetes, neurodegenerative disorders, immune function, inflammation, pain, 
mental disorders, and cardiovascular disease."
  
    
Scientists now believe that there are over 1,000 members of the 
functional lipidome, each of which is a new potential target for 
therapeutic intervention.
 
    
About Lpath:
    
Lpath, Inc., headquartered in San Diego, California, is the category 
leader in lipidomics-based therapeutics, an emerging field of medical  
science whereby bioactive signaling lipids are targeted for treating 
important human diseases. ASONEP(TM) (the systemic formulation of humanized 
form of Sphingomab(TM)) is an antibody against S1P that holds promise for 
the treatment of cancer and other diseases. A second product candidate, 
iSONEP(TM) (the ocular formulation of humanized Sphingomab), has 
demonstrated superior results in various preclinical AMD and retinopathy 
models. Lpath's third product candidate, Lpathomab(TM), is an antibody 
against LPA, a key bioactive lipid that has been long recognized as a valid 
disease target. The company's unique ability to generate novel antibodies 
against bioactive lipids is based on its ImmuneY2(TM) drug-discovery 
engine, which the company is using to add to its pipeline. For more 
information, visit http://www.Lpath.com
 
    
Forward Looking Statements
    
Except for statements of historical fact, the matters discussed in this 
press release are forward looking and reflect numerous assumptions and 
involve a variety of risks and uncertainties, many of which are beyond our  
control and may cause actual results to differ materially from stated 
expectations. For example, there can be no assurance that required clinical 
trials will be successful, necessary regulatory approvals will be obtained, 
or the proposed treatments will prove to be safe or effective. Actual 
results may also differ substantially from those described in or 
contemplated by this press release due to risks and uncertainties that 
exist in our operations and business environment, including, without 
limitation, our limited experience in the development of therapeutic drugs, 
our dependence upon proprietary technology, our history of operating losses 
and accumulated deficits, our reliance on research grants, current and 
future competition, and other risks described from time to time in our 
filings with the Securities and Exchange Commission. We undertake no 
obligation to release publicly the results of any revisions to these 
forward-looking statements to reflect events or circumstances arising after 
the date hereof.
 
Lpath, Inc.
http://www.lpath.com
		
Lpath preclinice demonstreazã eficacitatea Lpathomab (TM) ºi iniþiazã umanizarea procesului - Lpath Demonstrates Preclinical Efficacy Of Lpathomab(TM) And Initiates Humanization Process - articole medicale engleza - startsanatate