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To: redfrecknj who wrote (42286)9/25/2005 5:42:24 PM
From: Wyätt Gwyön  Respond to of 110194
 

Great Britain has 60.441 million people. The UK coverage level will eventually reach 24.2 %.


that is consistent with what i have read--about 25% coverage for the UK. i think a few of the Scandinavian countries with small populations have enough to cover the majority of their populations.



To: redfrecknj who wrote (42286)9/25/2005 5:43:08 PM
From: Elroy Jetson  Respond to of 110194
 
Few governments have been heeding Roche's advice. The company says it takes about 12 months to produce Tamiflu, which is one of the company's more complex drugs. At present, the company requires 12–18 months to supply new orders. A few countries, including Norway, Ireland, the U.K., and New Zealand, have enough capsules to treat up to 40% of their populations. Fewer than 20 countries, however, have stocked up on Tamiflu, many have not placed orders, and the supply of the drug worldwide is enough to treat only about 40 million people.

Roche Raises Output Of Bird Flu Drug
But firm will not meet demand for its antiviral drug Tamiflu if an avian flu pandemic breaks out

Chemical & Engineering News -- Jean-François Tremblay, C&EN Hong Kong -- August 29, 2005
pubs.acs.org

These days, in Hong Kong, it's still possible to walk into a drugstore, hand over HK$200 (U.S. $25) to a clerk, and walk out with a box of 10 capsules of Tamiflu, the antiviral drug that shows promise in treating humans for the deadly avian flu. Local pharmacists say they face no particular difficulty in stocking Tamiflu (oseltamivir phosphate) and that public demand for it is not particularly strong. F. Hoffmann-La Roche, which makes the drug, says 10 capsules are enough to treat a bout of the flu.

But the drug will become harder to find if the flu strain now spreading in Asian bird populations mutates into a form that can spread rapidly among people and precipitates a bird flu pandemic. In the spring of 2003, when Hong Kong was tensely fighting off SARS (severe acute respiratory syndrome), a teenager posted on a website the fake news that Hong Kong had been declared a diseased harbor, something that would disrupt food shipments to the territory. This caused thousands of people to rush to supermarkets in the middle of the afternoon to stock up on essentials like staple foods and bottled water.

Roche is well aware of the likelihood that demand for Tamiflu would surge during a bird flu pandemic, not just in Hong Kong, but worldwide. The company insists there is no shortage at present. But for the past few years, it has been advising health administrations around the world to stock up on this neuraminidase inhibitor. “We have been very clear that if a pandemic were to start tomorrow, the demand would be so steep that we could not guarantee that a government could get its supply,” David Reddy, head of Roche's pandemic task force, says.

Few governments have been heeding Roche's advice. The company says it takes about 12 months to produce Tamiflu, which is one of the company's more complex drugs. At present, the company requires 12–18 months to supply new orders. A few countries, including Norway, Ireland, the U.K., and New Zealand, have enough capsules to treat up to 40% of their populations. Fewer than 20 countries, however, have stocked up on Tamiflu, many have not placed orders, and the supply of the drug worldwide is enough to treat only about 40 million people.

To help overcome this apparent lack of preparedness, Roche says it will donate 30 million capsules of Tamiflu-enough for 3 million treatments-to the World Health Organization. The capsules would allow WHO to attempt to contain a pandemic in its early stages, regardless of whether the stricken area has its own stock of the drug.

Tamiflu Structure: pubs.acs.org

FLU FIGHTER Tamiflu (ball and stick) fights flu by blocking the active site of neuraminidase, a viral enzyme that cleaves terminal sialic acids from the surface of infected cells in order to enhance the release of newly assembled viruses.

Some health experts believe governments should consider resorting to compulsory licensing-that is, ignoring Roche's ownership of the drug to make up for the Swiss company's inability to cope with demand during a pandemic (C&EN, April 4, page 47). But Yusuf K. Hamied, chairman and managing director of Indian drug company Cipla, warns it would take about three years for his company, or any other firm, to be able to start producing Tamiflu because of the drug's complexity. And he adds that he cannot begin in earnest to plan to produce Tamiflu until he has some official assurance that he will not be accused of breaking the law for doing so.

“This is what I have been warning about,” he says, referring to his opinion that current drug patent laws do not serve the public interest. The leading supplier of drugs to the Indian market, Cipla is famously controversial for launching a generic version of an AIDS treatment consisting of three drugs that still enjoy patent protection in most countries. Until this year, the Indian government did not recognize patents on pharmaceuticals.

It's pointless to look at ways for outsiders to produce Tamiflu, Roche's Reddy says. He notes that Roche can meet demand expectations faster than anyone else because it is familiar with the challenging production process. To meet current orders, Roche has quadrupled production capacity since 2003, and it plans to double capacity again by next summer. Roche produces Tamiflu at three sites in Europe and one in the U.S.

Gilead Sciences, the U.S. company that invented Tamiflu and licensed the drug to Roche in 1996, is unimpressed by the Swiss firm's efforts surrounding the drug. In June, Gilead sent to Roche a request to end the licensing agreement and recover its rights to the drug. Gilead claimed in a press release that “Roche has not adequately demonstrated the requisite commitment to Tamiflu since its launch in the U.S. nearly six years ago, nor has it allocated the necessary resources to realize the potential of the product as a treatment and preventive for influenza.” Reddy says Roche is “disappointed” with Gilead's action and promises that this development will in no way affect Roche's efforts to boost capacity.

Meanwhile, there are some doubts that Tamiflu will be able to maintain its status as the most effective tool to contain a flu pandemic. For one, it has not been tested conclusively against avian flu. In a paper published this month in Foreign Affairs, Laurie Garrett, senior fellow for global health at the Council on Foreign Relations (a nonpartisan membership organization for foreign policy study), notes that the best way to treat the avian flu virus is as yet unknown. The World Health Organization recommends stockpiling Tamiflu mostly because few other options are available, she writes.

A possible alternative to Tamiflu is Relenza (zanamivir), another neuraminidase inhibitor that GlaxoSmithKline produces under license from Biota, an Australian antiviral drug discovery company. Like Gilead, which licensed Tamiflu to Roche, Biota is not happy with the way the larger company is promoting the drug. Biota has taken the extra step of suing GSK for alleged failure to effectively promote Relenza. Earlier this month, however, the German government placed an order for 1.7 million packs of Relenza, the biggest ever order for the drug. This follows the publication of a study this month in the British medical journal Lancet recommending Relenza as superior to Tamiflu in terms of effectiveness and side effects. Hong Kong, which is likely to be one of the first areas to be hit if there is a flu pandemic, stocks both drugs.

But Hong Kong has little faith in an avian flu vaccine that may become available soon, a spokeswoman for the Department of Health says. France's Sanofi Pasteur has begun testing a new vaccine that promises to immunize patients against bird flu. But even if the vaccine proves effective and Pasteur licenses it to anyone who asks, there may not be enough vaccine production capacity worldwide to inoculate more than a small fraction of the world population initially. Michael T. Osterholm, director of the Center for Infectious Disease Research & Policy at the University of Minnesota, Twin Cities, warned this month in another paper in Foreign Affairs that the world may have to go through one to three years of an avian flu pandemic before a vaccine becomes widely available.

Despite the emergence of these alternatives to Tamiflu, medical authorities worldwide are still betting on the Roche drug as their best weapon in the fight against an avian flu pandemic. If such a pandemic does break out, an event that seems ever more probable, Tamiflu will become a very precious substance if it proves its effectiveness against the new influenza strain.

Chemical & Engineering News
ISSN 0009-2347
Copyright © 2005
.



To: redfrecknj who wrote (42286)9/25/2005 5:58:36 PM
From: Elroy Jetson  Read Replies (1) | Respond to of 110194
 
The primary bottleneck is Shikimic acid, originally derived from a Japanese flower called shikimi-no-ki.

The Shikimic acid pathway is used by plants and bacteria to synthesize some amino acids and other compounds from carbohydrates.

The most common manufacturing process used today is an E.coli bacteria altered to be deficient in Shikimic Kinase, allowing Shikimic acid to slowly build up, yielding 35% product. A single batch, including purification, takes the better part of one year. The "just in time" "no inventory" ethic in America does not fit well with a process based on slow bacterial growth.

Complexity Of Tamiflu Manufacturing May Hamper On Demand Production

Chemical & Engineering News -- Amanda Yarnell -- August 29, 2005
pubs.acs.org

From the sourcing of the raw material to the production of capsules, it takes a full 12 months to make Tamiflu, according to Martin Karpf of Swiss drug giant F. Hoffmann-La Roche’s synthetic and process research group. Manufacture of the oral antiviral, thought to be the most promising weapon against avian influenza currently available, involves time-consuming routes to the starting material and steps that require potentially hazardous azide chemistry.

Process Diagram: pubs.acs.org

The 10-step commercial route uses the natural product (–)-shikimic acid as a starting material. This precursor is converted into a diethyl ketal intermediate, which is reductively opened to give a 1,2-epoxide. This epoxide is then converted into Tamiflu via a five-step reaction sequence involving three potentially toxic and explosive azide intermediates. This optimized route gives Tamiflu in 35% yield.

Initially, research quantities of (–)-shikimic acid cost more than $50 per gram, Karpf notes. This precursor “simply was not available on the world market in large amounts,” he says.

Needing to obtain a cheaper and more reliable supply of the starting material, Roche turned to Michigan State University chemist John W. Frost, whose lab had developed a strain of Eschericia coli that overproduces (–)-shikimic acid when fed glucose. Within a year and a half, Roche had figured out how to grow these bacteria on a commercial scale and determined how to extract and purify the (–)-shikimic acid.

An efficient route to extraction of (–)-shikimic acid from Chinese star anise also has become available, Karpf notes. Roche now relies on both fermentation and extraction to obtain ton quantities of (–)-shikimic acid, he tells C&EN. But with either method, isolation and purification of (–)-shikimic acid remains time-consuming.

The dependence on azide chemistry to convert the epoxide intermediate into a 1,2-diamine also poses a bottleneck to Tamiflu production. Safety and economic reasons have forced Roche to rely on a contract firm that specializes in azide chemistry to perform this sequence, Karpf says.

Roche has explored ways to speed up production (Chimia 2004, 58, 621). It has developed an azide-free allylamine route from the epoxide to Tamiflu. It has also crafted routes that don’t rely on (–)-shikimic acid: a Diels-Alder-based one that uses furan and ethyl acrylate as starting materials and another that relies on catalytic hydrogenation of an isophthalic acid derivative followed by enzymatic desymmetrization. And Frost has begun to develop a microbial synthesis of aminoshikimic acid, which could reduce the need for azide chemistry if used as a starting material (Org. Lett. 2004, 6, 1585). So far, however, none of these alternatives has measured up to the commercial route in terms of cost and efficiency.

Chemical & Engineering News
ISSN 0009-2347
Copyright © 2005
.