Lilly Gives Up on Schizophrenia Drug - Aug. 29, 2012

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Wednesday, August 29, 2012  |   |   |   |  SSCI Inc., A Division of Aptuit, will be offering "Pharmaceutical Solids: Essential Knowledge and Advanced Concepts," a two-day Pharmaceutical Solids Short Course for drug development scientists and related professionals. This event is designed for those who are looking to expand their knowledge of how solid state chemistry supports drug development, helping them to understand the importance of designing stable drug products early in the process. It will also have valuable information for IP attorneys and others concerned with drug development intellectual property. The two-day course will be held on October 18 and 19 at The Gleacher Center of The University of Chicago, and has been scheduled to coincide with the conclusion of the AAPS Annual Meeting for the convenience of attendees who are drawn to both of these industry events. To learn more and register for the Short Course, please go to http://www.ssci-inc.com/Information/ShortCourses/tabid/195/Default.aspx. •  Eli Lilly and Company (LLY) Gives Up on Schizophrenia Drug More... More Discontinuations News More Recalls and Warning News •  FDA Approves Janssen Pharmaceutical K.K.'s NUCYNTA® ER (tapentadol) Extended-Release Oral Tablets for Neuropathic Pain More... •  CardioComm Solutions Inc. (CCG) Receives FDA Approval to Market the HeartCheck™ ECG Monitor as a Prescription Product More... More Drug Approval News •  FDA Backs Approval of Abbott Laboratories (ABT)'s Humira for New Use More... •  Noven Pharmaceuticals Inc. (NOVN) Submits New Drug Application for Investigational Non-Hormonal Therapy for Menopausal Vasomotor Symptoms More... •  Proacta Inc. Announces IND Allowance for PR610 More... More BLA/NDA/ANDA News More IND News More MAA News •  Bayer AG (BAY.F) Says Blood Thinner Cuts Risk of Repeat Heart Attack More... •  ArQule, Inc. (ARQL) Plunges as Japanese Partner Temporarily Suspends Tivantinib Trial; Stock Down -1.3101 (19.55%) @ 1:19 PM EDT More... •  Novartis AG (NVS) Smoker's Cough Treatment Beats GlaxoSmithKline (GSK)'s Advair in Trial More... •  Eaton Scientific Announces Clinical Trial Plans for Tropine 3 - Company to Seek FDA Approval as Novel Prescription Drug for Non-Hormonal Treatment of Hot Flashes in Menopausal Women More... •  Amarin Corporation PLC (AMRN) Announces Additional Publication of MARINE Phase 3 Clinical Trial Results in the Journal of Clinical Lipidology More... More Phase III News More Phase II News More Phase I News More Pre-Clinical News More Post-Approval News Design and Development of Antibodies to Complex Protein Targets for Critical Assay Applications October 3, 2012 Online Webinar: Webinar Begins at 1pm EST. Examination of functional and therapeutic antibody-antigen x-ray crystal structures provides critical insight into B-cell epitope architecture. SDIX Genomic Antibody Technology™ is designed for development of antibodies that recognize conformational epitopes in critical assay formats such as sandwich immunoassays and flow cytometry and, enables targeting of antibodies to specific sites of native proteins. Antigen and antibody design strategies useful for different assay formats and classes of protein targets, including secreted and multipass membrane proteins are discussed. For more information please visit http://www.sdix.com/learn. •  Gene That Predicts Happiness in Women Discovered, University of South Florida Study More... •  Aspirin May Help Men With Prostate Cancer Live Longer, UT Southwestern Medical Center Study More... •  Softer Fast Food Restaurant Lighting and Music Can Cut Calorie Intake 18 Percent, Cornell University Study More... •  Tuning a Piano "Moulds the Mind," University College London and Newcastle University Study More... •  Boehringer Ingelheim Corporation Release: Large Scale Registry Shows Atrial Fibrillation Management is Suboptimal and Unequal Around the World More... More General Clinical Research News • BioCapital (Gaitherburg, Maryland) MedImmune, LLC Associate Clinical Program Manager Supports the Clinical Program Manager (CPM) and Senior Clinical Program Manager (Sr CPM) with supervision from the Line Manager in the planning and management of overall clinical operations execution for assigned clinical trial(s) including timelines, budgets, resources, investigational sites, vendors and key project deliverables in compliance with SOPs, Regulatory requirements and ICH/GCP guidelines and in alignment with departmental strategies and goals. • Pharm Country (Summit, New Jersey) Celgene Lead Clinical Research Scientist Provide leadership and direction to the assigned Clinical Research Scientists. Review work and project responsibilities within the group and assign task to ensure equitable distribution of responsibilities as well as leadership and development opportunities. • Biotech Beach (Irvine, California) Lab Support, A Division Of On Assignment Clinical Lab Scientist Perform diagnostic laboratory activities on the basis of standard operating procedures. Contribute to writing and adjusting of Standard Operating Procedures (SOP's). Consults with the Senior CLS regarding the daily work flow of the clinical laboratory and troubleshooting. • Genetown (Cambridge, Massachusetts) Vertex Clinical Process Associate Responsible for managing the lifecycle of relevant policies, SOPs, work instructions and business documents by serving as a workflow coordinator for the functions he/she supports. The Associate is also responsible for managing the execution of the development and revision of process documents by training authors on document standards, criteria and adherence to timelines. • BioMidwest (Northbrook, Illinois) Astellas Pharma US Clinical Study Manager Plan, initiate and execute assigned clinical studies with operational excellence. Be accountable for effective management of budgets, timelines and resources for assigned clinical studies and implementation of appropriate standards and processes to ensure clinical study quality. • Get Noticed! Add your resume to the BioSpace Career Center! • See more than 5,000 job postings in the BioSpace Career Center! 2012 Pharm Country Career Fair Job seekers can spend a day with HR representatives and Hiring Managers from top biotech, pharma, medical device and diagnostics companies in the tri-state area. Candidates with a 4-year degree in the life sciences and a minimum of 2-years of industry related experience are invited to attend. (Equivalent work experience may be considered in lieu of a four-year college degree. PhD and Postdoc candidates welcome.) Exhibiting companies are recruiting for positions in areas such as: QA/QC, clinical research, engineering, manufacturing, biostatistics, clinical data management, chemistry, regulatory affairs, and research. Job seekers may register here. • Pharm Country Career Fair, Bridgewater, NJ September 13, 2012 • Biotech Beach Career Fair, San Diego, CA September 20, 2012 • Biotech Bay Career Fair, Burlingame, CA October 3, 2012 • BioCapital Career Fair, Bethesda, MD October 9, 2012 • BioMidwest Career Fair, Lincolnshire, IL October 22, 2012 • Bio NC Career Fair, Durham, NC October 25, 2012 • Genetown Career Fair, Cambridge, MA November 5, 2012 More information about BioSpace's Career Fairs BioSpace White Paper Biotech Career Fairs For Job Seekers 101: Control Your Experience •  AcelRx Pharmaceuticals Receives Fourth and Fifth U.S. Patents for Small-Volume Oral Transmucosal Dosage Forms More... More Patent News •  PrecisionMed Inc. Launches Amyotrophic Lateral Sclerosis (ALS) Cerebrospinal Fluid Registry More... More Drug Product News New Emerging R&D and Clinical Trial Locations • Compare 5 new emerging R&D locations in terms of population, economic activity, healthcare infrastructure, and current R&D activity. • Analyze how clinical trial numbers are changing in China, India, and Eastern Europe. • Develop strategies for geographic outsourcing. Click Here for More Information. Hot Company NITTO DENKO Avecia Inc. 125 Fortune Boulevard Milford, Massachusetts 01757 U.S.A. Phone: 508-532-2500 Fax: 508-532-2503 Avecia, a recognized leader in the development and manufacture of DNA and RNA therapeutics, offers customized solutions and proven expertise that can seamlessly support your oligonucleotide product from small scale modeling to commercial launch. As a part of the Nitto Denko Corporation, Avecia's commitment to the future is driven by innovative ideas and flexible solutions, designed to provide our customers with the best in service, quality, and technology. 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