Wednesday, September 29, 2010

Lipid bubble vaccine delivery method patented

A new vaccine delivery method, which delivers vaccinations by small lipid bubbles has been patented. Vaccine News Daily reports that the vaccines is delivered in a lypozome, which inside contains a double layer of lipids.

This DNA molecule, Dow told PhysOrg.com, is fused to an immunogen, which is a protein fragment that the immune system mounts a specific attack against. The researchers said that the protein fragment could be part of an infectious organism or some other type of health hazard, like a cancer tumor.



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Tuesday, September 28, 2010

Global effort needed to reach an HIV Vaccine

The Guardian recently spoke with Mitchell Warren, executive director of the Aids Vaccine Advocacy Coalition, about the future of the HIV Vaccine. Progress was made earlier this year when Thailand conducted the first human clinical trial for a possible HIV vaccine.

When asked what the biggest setback was to developing the HIV vaccine, Warren stated science and funding. The human immune system is still somewhat of a mystery to scientists and funding is always a problem throughout development and the clinical trials.

Do you think an HIV vaccine will happen in the future? Warren states that scientists are going to have to globally unite in order to develop an effective vaccine. Is this possible?


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Wednesday, September 22, 2010

Who can you meet at Cell Based Assays & Bioanalytical Method Development 2010?

Over the past 5 years, the Cell Based Assays and Bioanalytical Method Development Conference has been the only place to learn from the scientists at the forefront of new approaches and solutions to the assay development obstacles you face everyday.

This year, hear the latest regulatory requirements, white paper authors and most recent case studies on new approaches to troubleshooting bioassay and bioanalytical challenges.

These companies will be there, will yours?

AAI Pharma Inc. * Alder BioPharmaceuticals * Allergan Inc. * Amgen Inc. * Biogen Idec * Bristol Myers Squibb * CBER FDA * Center for Molecular Medicine & Immunology * Cephalon Australia Pty Ltd * Charles River Laboratories * Facet Biotech * Food & Drug Administration * Genentech Inc. * Gregory Maschek * Human Genome Sciences Inc. * ImClone Systems * Immunogen Inc. * IRX Therapeutics * KaloBios * Laboratory of Cellular & Gene Therapy * Macrogenics Inc. * MedImmune Inc. * Pfizer * PPD Inc. * Process Confidence * Promega Corporation * Roche Diagnostics GmbH * SafeBridge Consultants Inc. * Sanofi Pasteur * Shire Human Genetic Therapies * TOLERX * Trion Pharma GmbH * University of Louisville James Graham Brown Cancer * US Pharmacopeia * Willem Oosterveen * Wyeth Pharmaceuticals



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Monday, September 20, 2010

Novartis breaks through on meningitis vaccine

Novartis UK has made a breakthrough that could result in a vaccination for Meningitis B according to the UK Gazette. The recent clinical trial proved to be successful. Meningitis B is the most common form of the disease, and 6%, approximately 1,200 cases in the UK, result in death. The vaccine should be effective against three different strains of the disease.

Mr. Steve Dayman, chief executive of Meningitis UK, "The latest results from this study are very encouraging and we hope these promising developments will ultimately lead to a meningitis B vaccine that will be given to children in this country. This is obviously an exciting development, and one which our supporters across the country will welcome. While we sense that we’re getting closer to finding an elusive vaccine for meningitis B, there is still more work to be done."

This blog is co-posted with The Drug Delivery Blog.


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Friday, September 17, 2010

Biosimilars market expcted to expand with health care reform

According to Pharma Live, by 2017, the biosimilars sector will reach $10 billion dollars. While healthcare reform is expected to hit the biotech sector in one way, the reform will allow them access to more patients in the United States, as well as rewarding biotechs for innovating and focusing on biosimilars.

Next week, we are hosting the Business of Biosimilars conference in Boston, MA. The event will delivers effective strategies to navigate scientific, regulatory, economic, and legal challenges you face to remain competitive in commercializing your biosimilar portfolio in the United States and abroad. We hope to see you in Boston!



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Thursday, September 16, 2010

As personalized treatment grows, patient access to biorepositories is shaky

The Richmond Times-Dispatch recently wrote an article looking at the growing importance of biostorage in the fight for personalized cancer treatment. As cancer moves away from the all-in-one chemotherapy treatments, it's moving towards using tissue samples to personalize the treatments for the patients. The storage of tumor tissue, both before and after treatment, is key to personalizing medicine. If patients want to have access to their tissue in order to participate in clinical trials, should the be allowed to transfer the tissue?

Another key part of the article is the ownership of the tissues that are stored. Should patients have access to and ownership of their tissues that are stored in biorepositories?



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Wednesday, September 15, 2010

Who can you meet next week at Business of Biosimilars?

The Business of Biosimilars event is taking place next week! It's not too late to register and join these industry leaders:

AARP * Abbott Laboratories * Alston & Bird * American Enterprise Institute * Amgen Inc * BD Medical Pharmaceutical Systems * BioProcess Technology Consultants * BNA * Boston Healthcare Associates Incorporated * Camargo Pharmaceutical Services * Celltrion Inc * Center for Medicine in the Public Interest * Charles River Laboratories * Covance Laboratories * Cureline * Dr Reddys Laboratories Inc * Ellen Bowe * EMEA * Engel & Novitt * ENTRA Pharmaceuticals Inc * Federal Trade Commission * Gedeon Richter USA Inc * Global Health Consulting * Goodwin Procter LLP * Greenstone Ltd * HartmannWillner LLC * Health Canada * Hospira Australia * Hospira Inc * Industry Standard Research * Ion Pharmaceuticals * IRS * Johnson & Johnson * LifeCell International Private Limited * Makovsky & Co Inc * Massachesetts Life Sciences Center * McDonnell Boehnen Hulbert Berghoff * Merck & Company Inc * Mergermarket Financial Times Group Pearson PLC * Montclair Bioequivalence Services LLC * North American Thrombosis Forum * Novartis * Organon NV * PAREXEL International LLC * Pfizer * Phillip Morris Intl R&D * Potomac Group * PPD Inc * Quintiles * Sandoz International GmbH * Sanford Bernstein * Sanofi Aventis * Smithers Group * STC Biologics Inc * Synthon Pharmaceuticals Inc * Takeda * The Center for Evaluation of Value and Risk in Health (CEVR) * The Dunn Group Inc * Trident Group LLC * Werthenstein BioPharma GmbH * Wolters Kluwer

To view all the presentations and speakers at our event, visit the Business of Biosimilars Agenda.



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Tuesday, September 14, 2010

Infectious diseases focus of research for vaccines

Infectious diseases are still a large cause of death around the world even though scientists have made major advancements in treating these diseases since the 1920s. Fierce Biotech states that there are currently 395 currently in the late stage of development, which means they are being reviewed by the FDA. Doctors are currently seeing that many of the diseases which currently have vaccines and medications are mutating and "Super Bugs" are forming. These drug-resistant viruses are increasing. In addition to working on those medicines and vaccines, scientists are taking a particular interest in diseases affecting third world countries including developing world, such as the Ebola virus, dengue fever, yellow fever, typhoid and cholera.



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Monday, September 13, 2010

Call for global approach to developing biosimilars

The European Generics Industry is calling for a world wide standard to develop biosimilars. Leaders believe standards need to be set for the industry world wide in order to create a consistent, scientific global approach in order to fully reach the potential that biosimilars can have world wide.

Greg Perry, director general of the European Generic Medicines Association (EGA), stated, "If healthcare systems are to continue to function long-term, we must address the importance of biosimilar monoclonal antibodies (MAbs) next. Science for MAbs is already here today and our industry is expecting a workable guideline."

Do you think a global, united front on biosimilars will aid the development of them? What could be the benefits of the scientists of the world having the same standards for developing biosimilars?



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Friday, September 10, 2010

Who Will You Meet at BIOREPOSITORIES 2010?

The nation's leading biobanking experts gather annually at The Biorepositories Event to cultivate a strategic perspective for sample management and exchange biorepository best practices throughout the sample lifecycle.

Bring your business cards and be ready to network with industry colleagues including:
AFRIMS * Alberta Health Services * Amgen Inc. * Arkansas Childrens Hospital Research Institute * Bahnson Environmental Specialists * BD Diagnostics * BD Medical Pharmaceutical Systems * Biobusiness Consulting LLC * BioRepository Resources LLC * BioStorage Technologies * bluechip * Boston VA Medical Center * Brady Corporation * California Cryobank * Carle Foundation Hospital * Celgene Corporation * Centers for Disease Control and Prevention * Childrens Healthcare of Atlanta * Cincinnati Childrens Hospital Medical Center * College of American Pathologists * Covance * Covidien * Crescendo Bioscience * Cryo Bio System * Cryoxtract Instruments LLC * Cureline Inc. * Defence Research & Development Canada Suffield * Department of Veterans Affairs * Dow Agro Sciences * Draper Laboratory * Duke University Medical Center * Eli Lilly & Company * ELPRO Services * Environmental Specialties * Fisher BioServices * Genentech * Gentris Clinical Genetics Inc. * Gilead Sciences Inc. * Goodwyn IRB * GSK * Hamilton-Storage Technologies Inc. * Henry M Jackson Foundation (CNRM) * Immune Tolerance Network * Indiana University * Indivumed Georgetown University * Indivumed Inc. * LifeNet Health * Matrical Bioscience * Mayo Clinic * Medtox Laboratories Inc. * Merck & Company Inc. * Millennium Pharmaceuticals Inc. * National Cancer Institute * National Marrow Donor Program * Novartis * Ohio State University* Pfizer Inc. * PPD * Regeneron Pharmaceuticals Inc. * Rutgers Environmental Health Sciences * Sensitech Inc. * Sofio Bio * STARLIMS * Stirling UltraCold * Takeda Global Research & Development Center * Vertex Pharmaceuticals Inc. * Wheaton Science Products

To find out more about the Biorepositories 2010, visit our webpage: http://bit.ly/9fpYBv
Download the 2010 Biorepositories Brochure: http://bit.ly/aXhfhk


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Thursday, September 9, 2010

The Changing Landscape of Biosimilars

The most recent issue of Pharmaceutical Technology Europe, they profile the landscape of biosimilars. In this issue they cover The Biosimilars Market of Today and Tomorrow, A SWOT analysis of the biosimilars market, Latest EU Guidelines, Launching and Commercializing Biosimilars and more. To discuss any of these articles in depth, join our Business of Biosimilars LinkedIn group where over 300 professionals around the world discussing the latest news and information in biosimilars.



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Wednesday, September 8, 2010

Cell Based Assays: An Interveiw with Xu-Rong Jiang, MedImmune

Speaker and Cell Based Assays Track Chair Xu-Rong Jiang, PhD, MD, Associate Director, Analytical Biochemistry, MedImmune, recently commented on the case study he'll be presenting at this year's conference taking place October 4-6, 2010, in San Francisco, California.

Download the MP3 here. Download the transcript here.
Visit the Cell Based Assays & Bioanalyitical Method Development agenda here.

First of all, can you tell us a little bit about your background?
Xu-Rong: I started cell based assay development back to 1998 at Geron for the early drug discovery. I have further developed cell based potency assays at Amgen since 2002. I was leading a group of scientists responsible for the development, qualification, validation of potency assays used for clinical and commercial biologic development. During the past 3 years, I have increasing responsibilities leading a large bioassay group responsible for development of cell based assays for low release biological characterization of biologics at MedImmune, a Biologic Subdivision of AstraZeneca. It has been my great pleasure working with Anne Reel, your program director, to present and co-chair at the Cell Based Assay Development conferences during the past 4 years. It is a very enriching experience for me.

Can you give us a preview of the case study you’ll be presenting this year? Xu-Rong: I have observed an increased level of interests and attendants of the conference during the past few years. Attendance of this conference really covers a great deal from the biopharmaceutical industry, especially for scientists the industrial leaders such as Genentech, Amgen, Biogen Idec, as well as for scientists from new emerging companies who wish to learn more from the industrial leaders and discuss their concerns. The case study I will present at this conference focuses more on a platform technology approach that will facilitate the development of homogeneous, fast and robust bioassays more effectively and efficiently. Specifically, this case study concerning the utilization of engineered cells for the development of cell based assays that could assess both Fab and Fc functionalities in a development- and QC-friendly manner.

What are you looking forward to at this year’s event?
Xu-Rong:
I think this year there are a couple of aspects that really have advanced from the past few years. Firstly, this year’s Cell Based Assays will be combined with Bioanalytical Method Development. So they are going to cover a broader range of topics, from cell based assays for potency, Fc effector function assessment, Nabs assays for immunogenicity, and assays utilized for PK/PD purpose.
Secondly, while I am serving on the advisory panel for the meeting organizers that we realized it would be great to attract regulators to present at the conference. This year,
2 Cell Based Assays & Bioanalytical Method Development Podcast: Xu-Rong Jiang, PhD
the conference has indeed attracted broader attendance, especially speakers from the FDA.
Last but not least, this year will held a Fc effector function session and a strategy white paper for the assessment of effector functions of therapeutic antibodies will be presented by An Song, PhD, Senior Scientist, Associate Director, BioAnalytical R&D, GENENTECH. I worked closely with her to co-author the manuscript that was submitted one month ago. All these aspects I believe will make this combined conference very unique.



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Tuesday, September 7, 2010

Business of Biosimilars Speaker Profile: James D. Chambers, Tufts Medical Center

James D. Chambers, Project Director
Center for the Evaluation of Value and Risk in Health
Tufts Medical Center

James will be participating in the panel discussion Meet Payer Needs – Formulary Placement and Pricing and Reimbursement Strategies.

James is a Project Director with the Center for the Evaluation of Value and Risk in Health at Tufts Medical Center. His research interests include what factors influence Medicare coverage decisions and the use of cost-effectiveness in the US health care system.

James graduated from Queens University in Belfast a degree in pharmacy and from the University of York with a masters degree in Health Economics. Currently he is studying towards his PhD in Health Economics from Brunel University in London.



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Wednesday, September 1, 2010

Biorepositories: An Interview with Tracie DeHart, Dow Agrosciences

Tracie DeHart, Dow Agrosciences, a speaker at this year's 2010 Biorepositories Conference, recently sat down with Courtney Leonard, the Biorepositories Conference Director to discuss some of the current trends in the biosciences industry..

They discussed:
-Tracie’s background in sample management
-Operating a biorepository in the biopharma industry versus the agrobio industry
-Setting up an in house biorepository
-And more!

Click here to download the transcript, and visit the Biorepositories 2010 webpage to download the podcast.



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