Big Pharma....
Cambridgeshire - Centre of the Pharmaceutical Universe?
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Prime Minister Tony Blair has said that he will sign an online petition supporting animal testing to take a stand against "a tiny group of extremists". His intervention came as international financial institutions pledged to stand by the pharmaceuticals group GlaxoSmithKline, 50 of whose shareholders were given an ultimatum by the group Campaign Against Huntingdon Life Sciences to sell their shares within 14 days or have their personal details published on a website. GlaxoSmithKline is a customer of Huntingdon Life Sciences in Cambridgeshire, the animal testing research laboratory which has been the subject of a long campaign by anti-vivisectionists. Animal rights activists target investors in GlaxoSmithKline [The Times - 9 May 2006] In 1998, Glaxo Wellcome (as it was then known before the merger with SmithKline Beecham) severed links with Huntingdon Life Sciences after a television documentary exposed animal cruelty at the laboratory, but reinstated its relationship a year later when new management took over.
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SEE ALSO: Minister defends animal experiments [BBC - 16 April 2002]
Cambridge monkey experiments inquiry [BBC - 24 May 2002]
PM criticised over animal testing [BBC - 14 May 2006]
Cambridge argues for monkey research [BBC - 25 November 2002] By taking a stand against "a tiny group of extremists" Tony Blair is ignoring the protests of peaceful, law-abiding people. How DEMOCRATIC is that? |
TAMIFLU
Also in Cambridgeshire is another pharmaceutical company, California-based Gilead Sciences Inc. which has its clinical development and regulatory operations based at Great Abington in Cambridge.
It was Gilead that developed Tamiflu, the antiviral medication believed to be effective against the deadly H5N1 strain of bird flu. Gilead then licensed Tamiflu to Roche Holdings in 1996 to get help manufacturing and marketing it, but Gilead complained that Roche wasn't aggressive on either front. Gilead, which was receiving royalties equal to about 10% of Tamiflu sales, took the unusual step of terminating its licensing agreement with Roche and going into arbitration to win back exclusive rights to the drug.
In November 2005, Roche Holdings and Gilead Sciences settled their dispute over Tamiflu and decided to work together to boost its supply. Gilead negotiated a bigger cut of Tamiflu revenue, 14% to 22% compared with 10% previously, and Roche paid Gilead $62.5 million in back payments. Roche, Gilead Sciences resolve Tamiflu conflict [Julie Schmit USA TODAY - 16 November 2005]
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The prospect of a bird flu outbreak may be panicking people around the globe, but it's proving to be very good news for US Defense Secretary Donald Rumsfeld and other politically connected investors in Gilead Sciences, the California biotech company that owns the rights to Tamiflu, the influenza remedy that's now the most-sought after drug in the world.
Rumsfeld was on Gilead's board for 12 years and was chairman from 1997 to 2001, when he joined the Bush administration and he still holds a Gilead stake valued at between $5 million and $25 million, according to federal financial disclosures filed by Rumsfeld.
The forms don't reveal the exact number of shares Rumsfeld owns, but in the past six months fears of a pandemic and the ensuing scramble for Tamiflu have sent Gilead's stock from $35 to $47. That's made the Pentagon chief, already one of the wealthiest members of the Bush cabinet, at least $1 million richer.
Rumsfeld isn't the only political heavyweight benefiting from demand for Tamiflu. Former Secretary of State George Shultz, who is on Gilead's board, has sold more than $7 million worth of Gilead since the beginning of 2005. Another board member is the wife of former California Gov. Pete Wilson. Rumsfeld's growing stake in Tamiflu [Nelson D. Schwartz CNN - 31 October 2005]
In July 2005 the Pentagon ordered
$58 million worth of Tamiflu for US troops.
On 15th March 2006 a group protesting against Procter & Gamble's use of animals in toxicity tests for cosmetics, toiletries and household products projected a stark message - 'PROCTER & GAMBLE TEST ON ANIMALS' - in 15ft high letters across the iconic 'Angel Of The North' sculpture on Tyneside. Angel of Mercy!
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In 1997 Rumsfeld became chairman of the Pharma-Biotech company Gilead Sciences Inc. and was on the board of Amylin Pharmaceuticals. It was under Rumsfeld that Searle got FDA approval for the controversial artificial sweetener, aspartame, which it marketed as NutraSweet. Some believe that the approval of aspartame was influenced by conflict of interest and that persons involved in the aspartame approval process were rewarded with high paying jobs or consulting positions. In April 2000, Pharmacia & Upjohn completed a merger with Monsanto and Searle creating Pharmacia. Following the merger, Pharmacia continued Searle's agreement with Pfizer to co-promote the NSAID Celebrex, which was originally co-developed by Searle and Pfizer. 2003 - Pfizer and Pharmacia Merge Monsanto is the manufacturer
of ethoxyquin - a potentially cancer-causing agent used as a preservative
in dry pet foods. Some veterinarians believe that ethoxyquin is a major
cause of disease, skin problems, and infertility in dogs. The use of ethoxyquin
in pet foods has not been thoroughly studied. Due to questionable data in the original study on its safety, Monsanto was required to perform a new, more rigorous study of ethoxyquin. This was completed in 1996. Even though Monsanto found no significant toxicity associated with its own product, in July 1997, the FDAs Centre for Veterinary Medicine requested that manufacturers voluntarily reduce the maximum level for ethoxyquin by half, to 75 parts per million. Monsanto are the company that gave us Agent Orange for military use in Vietnam, pesticides, beef growth hormones, PCBs and Dioxin. Monsanto is the global leader in developing and marketing Genetically Engineered (GE) products. In 2002, over 90 percent of GE hectares worldwide were planted with Monsanto's GE seeds. Monsanto: heading for disaster? [Greenpeace] |
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Many clinical trials are designed to fit desired outcomes... The following is an extract from House of Commons: Select Committee's Fourth Report and Part 8, Influence of the Pharmaceutical Industry on key groups 158. Throughout this inquiry we received much evidence about the influence of the pharmaceutical industry. We were told that it permeates the health service, regulatory and licensing bodies, research institutions, Government and the public perception of medicines. The extent of this influence was pithily expressed by Dr Richard Horton, editor of The Lancet - At almost every level of NHS care provision the pharmaceutical industry shapes the agenda and the practice of medicine. 180. Clinical trials can provide very important data about drugs but they do not always provide the clear information on drug safety and therapeutic effectiveness that is needed. It is claimed that many clinical trials are designed to fit desired outcomes or, worse, primarily for marketing purposes, rather than the advance of health care or scientific understanding. Dr Richard Nicholson, editor of the Bulletin of Medical Ethics, told us: A clinical trial was proposed to my ethics committee some years ago of Vioxx versus naproxen and we wondered to ourselves why on earth Merck want to compare this with naproxen. They did not give us the details initially and then when we asked and asked, we finally found out that they had already carried out major trials against the two major anti-inflammatory drugs and found absolutely no advantage of their drug. They were hoping that by comparing it to naproxen, which had just five per cent of the market, they would be able to show an advantage. |
![]() The Truth about the Drug Companies: How They Deceive Us & What To Do About It [Marcia Angell] Read about the unscrupulous aspects of the pharmaceutical industry & the short-comings of the pharmaceutical companies and the governmental regulatory bodies. |
181. In order for a drug to be licensed it has to show that it is more effective than a placebo, usually in two controlled trials. However, according to Prof Healy, companies can run 10 or more trials in carefully selected samples using instruments designed to pick up any effect and, even if the results show that the drug failed to beat placebo in the majority of trials, the drug may still be licensed. The trials producing negative results are commonly identified as failed trials rather than drug failures.
182. Whether the experimental drug is compared to placebo or a comparator drug will affect the outcome. Common flaws in trial design include the use of inappropriate comparator drugs, such as those associated with a higher risk of side-effects than others in the therapeutic group. Selection of dosage may also be used to skew results. Administration of a comparator drug in unduly low doses may result in reduced levels of efficacy. Administration of the comparator drug at relatively high dosages might make the test drug appear safer than it really is. These and other methods of trial design may show the new drug in a misleadingly positive light.
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All profits from the sale of jewellery items go towards the upkeep of rescued birds |
![]() Big Pharma: Exposing the Global Healthcare Agenda (Jacky Law) |