Friday, May 17, 2013

Taiwan, Israel urged to work together in medical device sector

 CNA May 1, 2013, 12:04 am TWNTAIPEI--Taiwan and Israel should step up cooperation in developing medical devices as both sides enjoy advanced technology and well-trained professionals, experts said yesterday at a seminar aimed at promoting such cooperation. Taiwan and Israel both have a medical device market worth over US$800 million, with their global market shares ranked at 27 and 26, respectively, said Chang Hsin-yi, a researcher at Taiwan's Industrial Technology Research Institute.The similar market scopes between the two countries have made it easier to forge a partnership, Chang explained at a seminar in Taipei held to encourage industry insiders to attend the 2nd Medical Devices & Health Information Technology Conference & Exhibition from June 10-13 in Tel Aviv, Israel. Both sides could establish more frequent information exchanges in medical services and medical equipment developments, added Chen Tzen wen, a seminar speaker and superintendent of Taipei Medical University Hospital."I'd suggest that Taiwan and Israel cooperate more on clinical trials because they help identify the patients' needs and accelerate innovative developments," said Chen.Moris Topaz, another seminar speaker and head of the Plastic Surgery Unit at the Haifa-based Hillel Yaffe Medical Center, said he hopes to interact more with Taiwanese talents to explore the forefront of medical developments. Currently taking charge of a specialty medical project in wound-healing — ranging from wounds caused by accidents to diabetes — Topaz said both sides could work toward developing surgical and rehabilitation programs in related fields. Israel has advanced medical device technologies and is one of the world's major exporters of medical devices, according to the Israel Economic and Cultural Office in Taipei, which organized the seminar.

 

Willemsen: 台灣GSK 6年花10億與台灣學研合作


NRPB Director Yang Pan-chyr (second left) and Glaxo Taiwan General Manager Thomas Willemsen display the memorandum May 7 in Taipei City. (CNA) Publication Date05/07/2013 Source Taiwan Today ByMeg Chang Taiwan's National Research Program for Biopharmaceuticals inked a memorandum of understanding on clinical vaccination trials with U.K.-based GlaxoSmithKline PLC May 7, further boosting local capabilities in this key biotech research area.Signed by NRPB Director Yang Pan-chyr and Glaxo Taiwan General Manager Thomas Willemsen in Taipei City, the pact calls for both organizations to collaborate on trialing vaccinations for diseases such as influenza type A and B, as well as tuberculosis and recurring lung cancer. Yang said the landmark agreement is Taiwan's largest clinical trial collaboration to date, and will focus on preventing some of the most common diseases around the world while benefiting millions of patients."We hope this memorandum will further cement our partnership with Glaxo and expect it to be the start of more joint projects with pharmaceutical firms worldwide," he said. "It should also help establish Taiwan as a front-runner in clinical trial research." According to Willemsen, Taiwan has always been an important Glaxo research partner in the Asia-Pacific region, with more than 20 experiments taking place in the country representing 13 percent of the firm's projects worldwide."Taiwan possesses distinctive advantages in clinical trial research, including the ability to fast-track results, high reliability of data, and a plethora of medical professionals with international experience," Willemsen said.Glaxo has spent over NT$1 billion (US$33.89 million) on joint R&D activities with local medical institutions since 2007, and remains committed to partnering with Taiwan going forward, he said. "We hope GSK can play a key role in helping Taiwan become a biotech research hub in Asia."With an annual budget of NT$2.5 billion, the NRPB aims to promote objective-oriented research for new pharmaceuticals and medical devices, as well as bridging the gap between academia and industry. It is supported by the Atomic Energy Council, Department of Health, Ministry of Economic Affairs and National Science Council.As part of government efforts to develop Taiwan's biomedical sector, the Council for Economic Planning and Development approved a proposal May 6 to build a hospital in northern Taiwan's Hsinchu Biomedical Science Park.The NT$5.5 billion facility has a planned capacity of 728 beds and will be operated by National Taiwan University Hospital under the auspices of the Department of Health.Construction of the hospital will begin next year, the CEPD said, adding that the first patients are expected to be admitted in 2018. (JSM)

 

Canada not planning H7N9 bird flu vaccine studies; will watch US results

 BY HELEN BRANSWELL, THE CANADIAN PRESS MAY 10, 2013Nurses collect patients' blood samples at a specialized fever clinic inside the Ditan Hospital, where a Chinese girl is being treated for the H7N9 strain of bird flu, in Beijing Sunday, April 14, 2013.(AP Photo/Andy Wong) TORONTO - Canada currently has no plans to ask its pandemic flu vaccine manufacturers to make trial batches of vaccine to protect against the new H7N9 bird flu, senior officials of the Public Health Agency of Canada have revealed.While the U.S. government has said it will ask several of flu vaccine manufacturers to start growing up batches of serum against the new virus this summer, Canada will watch, wait and learn from the work the U.S. does, the officials said in an interview with The Canadian Press."What we need to do in the international research-scientific community, the public health community is to complement each other. If the U.S. is doing something, we don't need to do it necessarily," explained Dr. Frank Plummer, head of the National Microbiology Laboratory in Winnipeg.Dr. John Spika, director general of the public health agency's center for immunization and respiratory infectious diseases, said doing this early work is more crucial for the United States, which will have to make a decision about whether to use an adjuvant with H7N9 vaccine, if the virus causes a pandemic. An adjuvant is a product that boosts the immune response to a vaccine, typically allowing a smaller dose to have a protective effect.The U.S. has not used adjuvants with flu vaccine before, but Canada used adjuvanted vaccine during the 2009 pandemic. And when the federal government signed new pandemic vaccine contracts in 2011, it stipulated it wants adjuvanted vaccine the next time it needs pandemic vaccine."So this step of doing some early clinical trials looking at immunogenicity is really going to be critical for the U.S. go-forward process. Whereas here in Canada, we've already made a decision on what kind of vaccine we're going to use. It's going to be an adjuvanted one," Spika said.Canada's main flu vaccine producer, GlaxoSmithKline, has a proprietary adjuvant, a product called ASO3. Sanofi Pasteur, which is Canada's secondary provider, does not currently have a licensed adjuvant that can be used with its flu vaccine.The new flu virus, which hit the world's radar at the beginning of April, has already caused 131 infections in China and Taiwan — which has reported a single case — and 33 of the infected people have died. H7 flu viruses have not circulated widely in people before and it's believed virtually everyone would be vulnerable to this new bird flu, if it fully adapts to person-to-person spread.The emergence of the virus is causing sleepless nights in pandemic preparedness circles. While it provokes severe disease in people, it causes no discernible illness in birds at this point. So finding where the virus is and how people are getting infected has been an enormous challenge. As well, the virus has some mutations that suggest it is partially adapted to infecting human respiratory tracts; experts say it appears to infect people more easily than other known bird flu viruses.Making matters worse is that fact that if the virus triggers a pandemic and vaccine is needed, there are multiple reasons to believe that producing an effective H7N9 vaccine could be hugely difficult. Those problems were spelled out in a prospective article the Journal of the American Medical Association published online late Thursday.The article, by researchers from the Center for Infectious Diseases Research and Policy at the University of Minnesota, outlined the long lead time for making flu vaccines, the modest protection offered by current seasonal vaccines and the limited but alarming data on vaccines against H7 viruses.Over the past few years the U.S. government has financed several small clinical trials testing vaccines for other H7 viruses, viruses like the H7N7 that infected around 90 people in the Netherlands in 2003 and the H7N3 that infected two people in British Columbia in 2004.The results have been dismal. Flu vaccine experts say H7 viruses appear to be the least immunogenic (immune-response inducing) of the bird flu viruses. In fact, in studies using killed virus vaccine — the type of vaccine used in seasonal flu shots — massive doses of serum failed to produce a protective response in most people.Seasonal flu shots contain 15 micrograms of antigen for each strain they protect against. In the H7 vaccine studies, 12 times that much vaccine (given in two shots) did not raise antibody levels to the degree that is considered protective."The bottom line is that it didn't do very much," flu vaccine expert Dr. John Treanor, chief of infectious diseases at the University of Rochester (N.Y.) Medical Center, said of the previous H7 vaccine trials. "In fact only a handful of people even had a measurable (immune) response."If even 90 micrograms of vaccine are needed to protect a person against the H7N9 virus, "global annual manufacturing capacity will be approximately 757 million doses," said the JAMA paper, the lead author of which is Michael Osterholm, director of the University of Minnesota centre."This is less than 15 per cent of the global need and much of it will not be available until six or more months after manufacturing begins," Osterholm and his colleagues wrote. "Adjuvants may augment vaccine capacity, but development of an adequate global vaccine supply will remain an unprecedented challenge."The U.S. Department of Health and Human Services does a risk assessment whenever a new flu virus emerges; the deliberations involve deciding on whether a trial lots of a vaccine should be made and tested.In this case, the decision has been made to go ahead with H7N9 vaccine clinical trials. The U.S. government has set aside $25 million for the development of vaccine seed strains and small vaccine batches for clinical studies, Gretchen Michaels, director of communications for the office of the assistant secretary for preparedness and response, said in an email. The current plan is that the manufacturers — who are currently still making next winter's seasonal flu vaccine — will start making the H7N9 vaccine in early summer.In Canada, no such work is currently envisaged.And the company which has the lion's share of Canada's pandemic flu vaccine contract, GlaxoSmithKline, said Thursday it has not yet taken possession of a seed strain for H7N9 vaccine. Janet Grdovich, communications manager for GSK Canada, said at this point she cannot say whether the GSK plant at Ste-Foy, Que., will started working with the H7N9 vaccine seed strain."GSK is taking routine preparedness measures and will respond appropriately to the situation, depending on how or if it develops further," she said.Spika acknowledged that the available evidence suggests that an H7N9 vaccine might be poorly immunogenic in people and that figuring out what a protective dose would be — even with an adjuvant — will take study. "And we're going to be able to get that information from the U.S. trials," he said.Spika and Plummer did not, however, rule out the possibility that Canada might do some work on H7N9 vaccines in the future."If it's scientifically required, we will do it," Plummer said."We're obviously monitoring the situation," Spika added. "It may well be, if this strain continues to emerge, and based on the results coming out of the United States, that we may want to move in that direction. But not at this point."Note to readers: This is a corrected story. An earlier version gave the wrong first name for Dr. John Treanor. NRPB, Glaxo ink clinical trial research pact

 

浙江華海藥業攜手Oncobiologics 開發生技學名藥(Humira, Rituxan, Avastin and Herceptin)


China Biotech In Review: Sagent Buys Out China JV Partner For $25 Million May 12 2013, 03:54Sagent Pharmaceuticals (NSDQ: SGNT), a Chicago-area maker of generic injectible drugs, will acquire its partner's 50% interest in a China JV for $25 million (see story). Chengdu Kanghong Pharmaceuticals owned the other half of the JV, which was established in 2006 to build an FDA/GMP compliant manufacturing facility. Sagent apparently expects to use the China facility to manufacture products that supply the China and US markets. ScinoPharm Taiwan (TSE: 1789) and Coland Holdings (TSE: 4144) formed an alliance to bring generic oncology drugs to mainland China. The alliance has selected several of ScinoPharm's APIs for development as injectible treatments. A third party will develop and manufacture the products, which will be co-marketed by Coland and ScinoPharm. Although Coland is listed in Taiwan and headquartered in Hong Kong, its operations, including a sales force, are in China. Zhejiang Huahai Pharma (SHA: 600521) joined with Oncobiologics, a New Jersey biologics startup, to form a partnership that will develop, manufacture and promote biosimilars. Huahai will have exclusive rights to make and market four Oncobiologics-developed biosimilars in China. The two companies will also sign a co-development and commercialization agreement to bring the four products -- generic versions of Humira, Rituxan, Avastin and Herceptin -- to 30 developed countries. Hutchison Chi-Med [AIM: HCM] expects to license global rights to fruqintinib, one of its novel small-cell cancer drugs, before year-end, according to CEO Christian Hogg. The company has been in due diligence discussions with potential partners, he added. Because the drug is a promising treatment for solid tumors, Chi-Med will conduct simultaneous clinical trials against several types of cancer, and the company wants a partner to help shoulder the financial burden.Zhejiang Beta Pharma and Amgen (NSDQ: AMGN) will form a joint venture to commercialize Amgen's Vectibix® (panitumumab) in China (see story). Vectibix is a treatment for colorectal cancer. In addition to being experienced with targeted therapies, Zhejiang Beta also has a well-established China oncology sales network. The JV will be 51% owned by Zhejiang Beta, with Amgen holding the remainder.

 

 

BioTek在台灣建立據點!!


BioTek Responds To Growing AP Market Needs With New Taiwan Office May 13, 2013 BioTek Instruments, Inc., continues their expansion in the Asia Pacific region with the opening of BioTek Taiwan, located in the Neihu District of Taipei. Mr. Jack Lu (Lu Wen-Chung), previously with Tseng Hsiang Life Science, was named General Manager of BioTek Taiwan at its inception in mid-April. The new office will focus on supporting current and potential customers, and increasing BioTek's brand presence in Taiwan."Taiwan's biotechnology and scientific sectors are expanding; supported by the government's focus and investment," noted Dominic Herring, BioTek's Business Development Manager. "Our direct office in Taiwan will allow us to provide local, strong and immediate applications and service support to our expanding customer base, in a market that continues to demonstrate high quality scientific research."

About BioTek Instruments, Inc. BioTek Instruments, Inc., headquartered in Winooski, VT, USA, is a worldwide leader in the design, manufacture, and sale of microplate instrumentation and software. These technologies are used to aid life science research, facilitate drug discovery, provide rapid and cost-effective analysis, and enable sensitive, accurate quantification of molecules across diverse applications. BioTek espouses a "Think Possible" approach that sets the tone for fresh ideas, unsurpassed customer service and original innovations. As such, they are often honored for local accomplishments and technological innovations, including Best Places to Work in Vermont, North American New Product Innovation Award for Workflow Solutions in Life Sciences and Drug Discovery Product of the Year – Scientists' Choice Award.SOURCE: BioTek Instruments, Inc.

 

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