242 Des Chenaux Ch., Vaudreuil-Dorion, QC J7V 9E5, Canada
Email ng629370@westpost.net; T 450 510-9546; F 450 510-0172; C 514 796-9546 ________________________________________ PROFILE Pharmaceutical and Biotechnology preclinical research manager with over 25 years experience, primarily in anti-infectives. Developed and implemented drug discov ery strategies, including NIH grant applications; initiated and led research pro jects; provided input to INDs; led collaborations with corporate partners; mento red colleagues and subordinates. Played key role in the discovery and development of the monocyclic *-lactam aztr eonam (Azactam(R)) and the cephalosporin-quinolone conjugate Ro 23-9424. Co-disc overed and patented: a new class of *-lactamase inhibitors. Also, a fungal-speci fic histone deacetylase (Hos2) and a Hos2 inhibitor (MG3290) which potentiates a ntifungal azoles and is currently in clinical development as MGCD290. Expertise and experience in (bio)chemistry, enzymology, cell biology, molecular biology. Deep, multi-disciplinary understanding of the drug discovery and develo pment process. Effective and consistently productive team leader; creative, ener getic, flexible, results-oriented. Excellent interpersonal and communication ski lls (over 30 invited talks). Strong publication record (close to 200 research pa pers, abstracts and reviews; two books). Dual citizenship (US, GR/EU). ________________________________________ PROFESSIONAL EXPERIENCE Preclinical Research Consultant, Anti-infectives (2008-present) Corporate clients: Novexel Pharmaceuticals (Romainville, France), Janssen Pharma ceutica (Beerse, Belgium). TEMPLE UNIVERSITY SCHOOL OF MEDICINE, Dept. of Microbiology & Immunology (Phil adelphia, PA, USA) Adjunct Professor (1999-present) DRUG RESISTANCE UPDATES (http://www.elsevier.com/wps/find/journaldescription. cws_home/623026/description) Bimonthly review journal published by Elsevier Science, UK (2008 Impact Factor 9 .4, 5-year Impact Factor 7.5) Founder and Editor-in-Chief (1997-2009) NOVABAY PHARMACEUTICALS (Emeryville. California, USA) Vice President, Research (2007-2008) Led preclinical research (Medicinal Chemistry and Biology). Developed and imp lemented strategy, recruited scientists, introduced a new anti-infective discove ry project. Led collaboration on topical anti-infective N-chloroamines with Alcon. Collab oration included development of a lead N-chloroamine, NVC-422. Worked closely with Business Development towards in-licensing antibacterial ta rgets and compounds. Provided insights and competitive intelligence on anti-inf ectives. Prepared presentations for scientific conferences and corporate meetings with potential investors and corporate partners. METHYLGENE INC. (Montreal, Canada) Vice President, Infectious Diseases (2003-2006) Initiated antifungal project based on company's histone deacetylase (HDAC) inh ibitor platform. Co-discovered a new fungal HDAC target whose deletion sensitiz es fungi to antifungal azoles and a fungal-specific HDAC inhibitor which potenti ates antifungal azoles in vitro and in vivo. Led two collaborations: with Merck (class C *-lactamase inhibitors that potent iate *-lactam antibacterials) and with Taiho (mammalian HDAC inhibitors with ant i-oncotic activity). Taiho collaboration included clinical development of a lea d compound, MGCD0103 (MG5837). Provided scientific leadership, insights and competitive intelligence in other research programs (multitarget kinases, non-oncology HDAC inhibitors). Prepare d presentations for scientific conferences and corporate meetings with potential investors and corporate partners. Formulated strategy for transitioning antifungal project from preclinical to c linical research. Drafted brochures for out-licensing, IND. NEWBIOTICS INC. (San Diego, CA, USA) Senior Director, Life Sciences (2001-2003) Led three research groups: oncology, enzymology/biochemistry, infectious disea ses. Integrated biology with chemistry in the design and preclinical development of antimicrobial and anticancer agents based on company's Enzyme-Catalyzed Therape utic Activation (ECTA) platform. DUPONT PHARMACEUTICALS (Wilmington, DE, USA) Principal Scientist (1997-2001) Recruited scientists and initiated antifungal research projects (inositol phos phoceramide synthase, N-myristoyltransferase, ergosterol synthesis) that include d access to natural products through outside collaborations. Directed developme nt of assays suitable for high throughput screening, transfer to Lead Discovery group, lead follow-up and evaluation. Worked closely with Product Planning and Acquisition group towards in-licensin g antifungals: sordarins from Glaxo (GSK), aureobasidins from Takara-Shuzo and F K-463 (micafungin) from Fujisawa (Astellas). Acted as a resource within infectious diseases, providing competitive intellig ence to senior management. PRINCETON UNIVERSITY, Dept. of Molecular Biology (Princeton, NJ, USA Visiting Fellow (1995-1997) Upgraded knowledge and skills in molecular biology Investigated ceramide-mediated signal transduction in Saccharomyces cerevisiae . Preclinical Research Consultant, Anti-infectives (1995-1997) Corporate clients: Affymax, Bayer AG, Hoffmann-La Roche Ltd, ISIS Pharmaceutical s, Panlabs Inc., Procter and Gamble Pharmaceuticals, Schering Plough, Versicor I nc. HOFFMANN-LA ROCHE INC., Roche Research Center (Nutley, NJ, USA Distinguished Research Leader (1992-1995) Directed research in the post-translational modification of p21ras proteins, i ncluding assay development and inhibitor design. Proposed molecular targets (eukaryotic topoisomerase II and protein tyrosine k inase) and strategy for anticancer drug design. Research Leader (1988-1992) Directed several projects in antibacterial research: initiation factor 2 (IF- 2), elongation factor Tu (EF-Tu), bacterial transport of quinolones, *-lactams a nd *-lactam-quinolone conjugates, mechanism of action and resistance of *-lacta m-quinolone conjugates. Worked closely with Anti-Infective Chemistry group in the design and evaluatio n of new antibacterials, of which one (Ro 23-9424) entered phase I clinical tria ls. Acted as a resource within infectious disease research. Provided competitive intelligence to senior management. Research Investigator (1985-1988) Developed mode-of-action based screens: replicative DNA, RNA, and protein bios ynthesis assays in permeabilized cells. Established mode of action of (2,3)-*-methylene penams (cyclopropylpenams), qu inolones and quinolone analogs, cephalosporin-quinolone conjugates. Research Group Chief (1984-1985) Examined inhibition of E. coli and S. aureus DNA gyrase by quinolones; correla ted with antibacterial activity. Advised on bacterial cell wall biosynthesis projects: peptidoglycan transpepti dase, DD-carboxypeptidase, penicillin-binding proteins E.R. SQUIBB & SONS INC., Squibb Inst. Medical Research (Princeton, NJ USA) Senior Research Investigator 1980-1984 Developed assays for cholesterol biosynthesis, particularly hydroxy-3-methylgl utaryl coenzyme A reductase, in human fibroblasts. Developed cell-based assays for inhibitors of ergosterol synthesis in S. cerev isiae and Candida albicans. Developed biochemical assays for chitin and glucan biosynthesis in S. cerevisi ae and C.albicans; tested antifungals and rationally designed inhibitors. Developed mode-of-action based screens for bioactive microbial products. Research Investigator (1977-1980) Contributed to the clinical development of aztreonam by providing key preclini cal information that pointed to its advantages and limitations. Established mode of action of monobactams: binding to penicillin-binding prot eins (PBPs), effects on penicillin-sensitive enzymes and on cell morphology. Surveyed bacterial PBPs and correlated binding of *-lactam antibiotics with an tibacterial activity. Examined the active site of Streptomyces R61 DD-carboxypeptidase and its inter action with monobactams. ________________________________________ EDUCATION AND TRAINING HARVARD UNIVERSITY, Biological Laboratories (Cambridge, MA, USA) Research Fellow in Biology (1976-1977); Advisor: Jack L. Strominger, M.D.) Research Project: Interaction of penicillin with Bacillus subtilis DD-carboxy peptidase. YALE UNIVERSITY, Chemistry Dept. (New Haven, CT, USA) Ph.D. Student in Biochemistry (1971-1975); Advisor: A. Ian Scott, Ph.D. Research Projects: Biosynthesis of the aromatic polyketide 6-methylsalicylic a cid. Biosynthesis of the tetrapyrrole ring of vitamin B12. MILLS COLLEGE (Oakland, CA, USA); 1968-1971 B.A. with honors in Chemistry (minor in Biology). ________________________________________ PROFESSIONAL MEMBERSHIPS American Academy of Microbiology (Elected Fellow, 1992) American Association for the Advancement of Science (1977) American Association for Cancer Research (1994) American Chemical Society (1977) American Society for Biochemistry and Molecular Biology (1977) American Society for Microbiology (1977) PROFESSIONAL REFERENCES Available upon request PUBLICATIONS, ABSTRACTS, INVITED TALKS Available upon request ________________________________________