Current Issue: April 1, 2010 Next Issue: September 2010
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Rachel Kiddell-Monroe has seen firsthand the impact of a lack of affordable medicines in the developing world. The Montreal-based physician, with Doctors Without Borders for 16 years, worked in a hospital ward in Rwanda full of AIDS patients, many within days of dying. It was 1994 and there was no AIDS treatment available in Africa. She called pharmaceutical companies to try to get treatment for her patients, and was told the lifelong treatment would cost about $12,000 per patient each year, and that no one was willing to fund it.
Sixteen years later, Canada now has legislation to get affordable medicines, like HIV/AIDS drugs, to people in the developing world. Canada’s Access to Medicines Regime, or CAMR, was passed in 2004, with Kiddell-Monroe playing a key role in championing the legislation. But CAMR is “seriously flawed,” says Richard Elliott, executive director for the Canadian HIV/AIDS Legal Network. The five-year-old legislation has only been used once, with an order of drugs shipped to Rwanda. That’s why New Democrat MP Judy Wasylycia-Leis introduced Bill C-393. The private member’s bill aims to reform CAMR and streamline the process of getting patented pharmaceuticals to developing countries. The bill passed second reading in the House of Commons in December 2009, and is now at the committee stage. Bill C-393: the solution to “flawed” legislation? Jillian Köhler, University of Toronto pharmacy professor and co-author of a 2007 report on CAMR’s policy gaps, says CAMR was “designed to fail from the get go.” “The legislation fails to give commercially-viable incentives for the generic drug industry, " Kohler says. "It was cumbersome for the developing countries to use, and it simply was too complex to get drugs to people quickly.” An example, Köhler says, is the situation with Apotex. The Toronto-based company was the first and only generic drug manufacturer to use CAMR to ship an order of HIV/AIDS drugs to Rwanda in Sept. 2009. Apotex says it faced so many hurdles using the legislation that it wouldn’t likely try it again, according to a Sept. 18, 2009 statement from Jack Kay, the company’s president. “The bottom line is: we need to make [CAMR] easier to use,” says Köhler. Tweaking [CAMR] wouldn’t cost Canadian taxpayers a single cent and could potentially save many, many lives. “It risks becoming a one-hit wonder,” says Elliott. Wasylycia-Leis says C-393 addresses those problems. “It speeds up the process, takes out the bureaucracy and red tape, and becomes much more efficient,” she says. Not everyone supports C-393. It passed second reading in the House of Commons by 143 to 127 votes, with most Conservatives opposing the bill along with a handful of Liberals. CAMR not the only answer One of the opposed is Liberal MP Marc Garneau, the party’s industry, science and technology critic. While Garneau says he supports getting medicines to developing nations, he doesn’t agree with C-393. He says countries in need of medicines are already getting them at a lower cost from other countries, like India and South Africa. He also says there is a lack of infrastructure in place in developing countries to receive, store, transport, and administer medicines. Garneau instead proposes a model where developing countries make their drug needs known to the Canadian International Development Agency. CIDA passes the order on to both big pharmaceutical companies and generic drug companies, who then bid for the order. Also opposed to C-393 is Rx&D, a lobby group representing Canada’s research-based pharmaceutical companies. Russell Williams, the group’s president, said in a March 29 statement that “C-393 would remove a number of critical safeguards that were consciously placed in CAMR by parliament.” Williams also said pharmaceutical companies represented by Rx&D have provided more than $250 million in donated medicine to developing countries since 1990. Opposition arguments don’t “hold water” Wasylycia-Leis says “it makes no sense” for big pharmaceutical companies to oppose C-393. “It’s power politics,” she says. “Anything that leads to generic drug companies playing a greater role is a threat to Big Pharma.”
Elliott believes many of the MPs who opposed C-393 at second reading were “accepting misdirections” from big pharmaceutical companies. He says this has led to a few MPs “caving to corporate pressure.” Kiddell-Monroe, also president of the board of directors for Universities Allied for Essential Medicines, a global private non-profit organization, says none of the arguments against C-393 “hold water.” “Tweaking [CAMR] wouldn’t cost Canadian taxpayers a single cent and could potentially save many, many lives,” she says. Wasylycia-Leis is not opposed to Marc Garneau’s proposed model. “It’s fine to pursue other additional ways of getting drugs to Africa, but that doesn’t negate the need for my bill,” she says. Supporters know there are still many hurdles ahead for C-393 to become law. “This is not smooth sailing by any means,” says Elliott. “There’s definitely going to be an effort from Big Pharma and its allied MPs to vote the bill down, or possibly even kill it.” For now, the bill is waiting for an Industry committee meeting to be scheduled to be considered, which Wasylycia-Leis believes will take place sometime before June. |
Statistics: a dire need for medicine
Source: Canadian HIV/AIDS Legal Network; Policy Gaps in the Canadian Access to Medicines Regime; Liberalsenateforum.ca CAMR's flaws
Out of synch with commercial realities:
Does not meet developing country health needs:
Source: Policy Gaps in the Canadian Access to Medicines Regime: A Submission to Industry Canada and Health Canada; Leslie Dan Faculty of Pharmacy, University of Toronto What does Bill C-393 do?
Under Bill C-393, a single open-ended license for each drug would authorize generic manufacturers to export medicines patented in Canada to any eligible country specified in the legislation, in any quantity. With a “one-license solution … the process doesn’t have to be repeated every time, for every drug, for every country,” says Wasylycia-Leis. The generic drug manufacturer would still pay royalties to the company holding the patent for a drug, just as under CAMR. Bill S-232: What happened?
Liberal Senator Yoine Goldstein tabled Bill S-232, similar to C-393. It was being debated in the Senate but died when Parliament was prorogued. Bill S-232 was "essentially the same" as Bill C-393, says Kiddell-Monroe. Although both bills were passed before Parliament was prorogued, there are different rules for bills in the Senate and the House of Commons. Bill C-393 stayed alive. |
Thanks for this very well put together article and multimedia. This message is so important to so many people in Africa who do not have a voice. Through the many efforts of the Grandmothers to Grandmothers groups and National Advocacy Campaign, as well as through other organizations, awareness has increased but there is a long way to go yet.