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Medicine alumnus and is currently professor and chairman of Psychiatry & Behavioral Sciences at the Medical University of South Carolina MUSC ; and a clinical professor of Psychiatry and Behavioral Sciences at Emory University School of Medicine. At MUSC he oversees an active psychiatry department consistently ranked among the top departments in the United States for research support. He is also executive director of the Institute of Psychiatry at MUSC, which includes a 90-bed inpatient hospital. The Institute was recently named one of the best hospitals in the nation for treatment of psychiatric disorders by U.S. News & World Report, and for the last two years has been named Hospital of the Year by the National Alliance for the Mentally Ill NAMI ; of South Carolina. "Dr. Oldham brings to Menninger a wealth of clinical expertise and experience working with complex medical and psychiatric systems, " said Ian Aitken, president and CEO of The Menninger Clinic. "His inter national reputation as a leader in psychiatric medicine and specialization in personality disorders is a tremendous asset to The Clinic and our affiliations with Baylor College of Medicine and The Methodist Hospital. We are pleased he is joining our team at this exciting time in our history." In his new role, Dr. Oldham's goals include continuing Menninger's shared vision with its partners to build a new international behavioral health campus located near the Texas Medical Center and working closely with Baylor College of Medicine to continue developing leading mental health patient care, research and education. After receiving a master's degree in neuroendocrinology from Baylor College of Medicine in 1966 and a medical degree from Baylor College of Medicine in 1967, Dr. Oldham completed his psychiatric training at Columbia University College of Physicians and Surgeons and the New York State Psychiatric Institute, and his psychoanalytic training at the Columbia Psychoanalytic Center. He holds board certification in psychiatry, psychoanalysis and forensic psychiatry and is considered an expert in the area of personality disorders, about which he has written and lectured extensively. Where Q3 is relevant and there is a need to determine the concentrations of individual hydrocarbons, pentane is used as the main extraction solvent, but re-distilled dichloromethane is used as part of the sample clean-up procedure. Samples are then analysed by high resolution capillary Gas Chromatography with a flame ionisation detector. The range of the application is 0-20 microgram litre. Reference: SCA. Determination of very low concentrations of hydrocarbons and halogenated hydrocarbons in water. 1985 HMSO. ISBN 0 11 752004 7. Other solvents that have been used to extract organic compounds from sediments and water are: CFC-113 for polyaromatic hydrocarbons 1991 ; , ethyl acetate; dichloromethane for benzo a ; pyrene, nitrophenols and nitroaniline USEPA CLP method 1990 n-hexane for organochlorine pesticides and lamotrigine.

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Dyax Corp. DYAX ; , Cambridge, Mass. Genzyme Corp. GENZ ; , Cambridge, Mass. Product: DX-88 Business: Cardiovascular Molecular target: Kallikrein Description: Yeast-derived recombinant kallikrein inhibitor protein Indication: Treat hereditary angioedema HAE ; Endpoint: NA Status: Interim Phase II data Milestone: Start Phase III 1H05 file BLA 2006 ; Interim data from an open-label, dose-ranging Phase II EDEMA2 trial based on 61 HAE attacks in 34 patients showed that DX-88 was well tolerated and could elicit rapid clinical responses. The clinical response in this trial is defined as relief of HAE symptoms within 4 hours of treatment. The median time to clinical response was 35 minutes. DX88 has Orphan Drug designation to treat HAE in the U.S. and Europe and Fast Track designation in the U.S. Data will be presented at the American Academy of Allergy Asthma and Immunology meeting in March in San Antonio. Elite Pharmaceuticals Inc. ELI ; , Northvale, N.J. Product: Naltrexone Business: Neurology Molecular target: NA Description: Naltrexone formulated with abuse resistant technology for narcotic analgesics Indication: Treat chronic pain Endpoint: Blood levels Status: NA Milestone: NA In an open-label, U.S. study in 12 subjects, food intake did not affect the performance of the formulation and no quantifiable levels of naltrexone were observed at a limit of quantification LOQ ; of 7.5 pg ml. The study was designed to evaluate the effect of food on absorption of naltrexone. Indication: Treat chronic pain Endpoint: Blood levels Status: NA Milestone: NA Data from an open-label study in 6 subjects showed that no quantifiable blood levels of naltrexone were observed at a limit of quantification LOQ ; of 7.5 pg ml. The study was designed to observe blood levels of naltrexone for 7 days following dosing under fed conditions. Indication: Treat chronic pain Endpoint: Blood levels Status: NA Milestone: NA Data from an open-label, U.S. study in 12 patients comparing naltrexone formulations showed that no quantifiable blood levels of naltrexone were released at a limit of quantification LOQ ; of 7.5 pg ml, when naltrexone was in its unaltered form. Data from the physically altered crushed formulation showed that significant amounts of naltrexone were released and absorbed with a Cmax of 3, 330 pg ml at the 30 minute time point. Erasmus University Medical Center, Rotterdam, the Netherlands Product: Pegylated interferon alpha Business: Infectious Molecular target: NA See next page.

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