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 Biologic drugs started as replacement 
                    therapies such as Growth hormone and Erythropoietin broadened 
                    into a big class of therapeutics with the addition of antibodies. 
                    There are a number of blockbuster drugs on the market with 
                    phenomenal therapeutic benefit in diseases such as Oncology, 
                    Rheumatoid arthritis and others. Since biologic therapies 
                    in general have high success rate compared to small molecule 
                    drugs, many big pharma and biotech companies are aggressively 
                    pursuing Biologics now and comprise roughly half of the clinical 
                    pipelines. Significant improvements have been made in the 
                    last decade on generating production of lasting biologic therapies, 
                    fully human monoclonal antibodies as therapies and phage display 
                    technologies. Active efforts in identifying minimal regions 
                    required for therapeutic benefit also identified smaller biologics 
                    such as peptibodies and nanobodies.Narender R. Gavva
 The 2nd ICDDT to be held in Dubai in February 2010 will address 
                    all active areas of research and development in 'Biologics' 
                    as therapeutics. To name a few, there will be presentations 
                    on protein therapeutics (both enzyme replacements and 2nd 
                    generation therapeutics), antibody therapeutics, Biosimilars 
                    and technologies that are used to improve biologics stability, 
                    metabolism and production.
 Amgen Inc
 CA, USA
 
 
 
  
 
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	            | 
 |  | Dr. 
                    Gavva received his PhD in 1992 from The University of Hyderabad 
                    followed by a Postdoctoral Fellowship at Section of Molecular 
                    and Cellular Biology, University of California at Davis, CA. 
                    Narender joined Amgen Inc. in 1999 and advanced through roles 
                    of increasing responsibility. In his current position, he 
                    is leading an in vitro pharmacology group that supports assay 
                    development, focused screens, lead optimization efforts, and 
                    evaluation of new technologies. Narender is experienced in 
                    full drug discovery cycle including validation of targets, 
                    HTS, automation, hit/lead identification, lead optimization, 
                    and clinical candidate selection. Narender is a great team 
                    player and has an excellent ability to plan and complete research 
                    programs.http://www.linkedin.com/pub/narender-r-gavva/3/6b1/36b |  
	
	
	            |  Pharma R&D Achievements: By cross-functional team 
                    leadership, Narender moved forward research programs in both 
                    small and large molecule drug discovery. Narender contributed 
                    significantly to clinical candidates such as AMG 517 and AMG 
                    628. Experienced in ion channels, GPCRs, kinases, transcription 
                    factors, and project management.
 
 Scientific Contributions:  Authored and 
                    published 30+ papers in research areas of drug discovery, 
                    lead optimization, pharmacology, clinical trials, molecular 
                    biology, biochemistry, and gene regulation. Gave invited lectures, 
                    presentations at several scientific conferences (APS, EB, 
                    SBS, Spring Pain Research Conference, IBC ACT, Arrowhead pain 
                    conference, etc). Serves as Editor-in-Chief (The Open Drug 
                    Discovery Journal), EABM (The Open Pain Journal), and as an 
                    ad hoc reviewer for several journals (AJP, JBC, JBS, JCI, 
                    J. Neurosci, JPET & Mol. Pharm).
 
 Recent publications:
 
                    
                      Wong GY, Gavva NR. Therapeutic potential 
                        of vanilloid receptor TRPV1 agonists and antagonists as 
                        analgesics: Recent advances and setbacks. Brain Res Rev. 
                        2009 Apr;60(1):267-77.
                      Gavva NR. Body-temperature maintenance 
                        as the predominant function of the vanilloid receptor 
                        TRPV1. Trends Pharmacol Sci. 2008 Nov;29(11):550-7.
                        
                      S.G. Lehto, R. Tamir, H. Deng, L. Klionsky, 
                        R. Kuang, A. Le, D. Lee, J.-C. Louis, E. Magal, B.H. Manning, 
                        J. Rubino, S. Surapaneni, N. Tamayo, T. Wang, J. Wang, 
                        J. Wang, W. Wang, B. Youngblood, M. Zhang, D. Zhu, M. 
                        H. Norman, and N. R. Gavva. Antihyperalgesic effects of 
                        (R,E)-N-(2-hydroxy-2,3-dihydro-1H-inden-4-yl)-3-(2-(piperidin-1-yl)-4-(trifluoromethyl)phenyl)-acrylamide 
                        (AMG8562), a novel transient receptor potential vanilloid 
                        type 1 modulator that does not cause hyperthermia in rats.J 
                        Pharmacol Exp Ther. 2008 Jul;326(1):218-29.
                       Gavva NR, Treanor JJ, Garami A, Fang 
                        L, Surapaneni S, et al. Pharmacological blockade of the 
                        vanilloid receptor TRPV1 elicits marked and persistent 
                        hyperthermia in humans Pain, 2008 May;136(1-2):202-10. |  |