[Ip-health] MSF op-ed in the Times of India: Don't swallow this pill

thiru at keionline.org thiru at keionline.org
Wed Jan 19 03:56:19 PST 2011


http://timesofindia.indiatimes.com/home/opinion/edit-page/Dont-swallow-this-pill/articleshow/7312903.cms

Don't swallow this pill
Unni Karunakara, Jan 19, 2011, 12.00am IST

Are the European Union and its multinational pharmaceutical companies now
pressuring the Indian prime minister's office? In recent months, as
negotiators from India and Europe have been thrashing out the details of a
free trade agreement to be signed within months, people living with HIV
have been hitting the streets. From New Delhi to Nairobi and Brussels to
Bangkok, they have been protesting against the very real threat posed to
India's ability to supply life-saving generic medicines to people across
the developing world.

Publicly, both sides have assured that the trade deal will not harm access
to the affordable generic medicines, and have reiterated, as if by rote,
the primacy of people's health over economic interests. But the Indian
press now reports that the PMO, under pressure to conclude the deal, has
asked the concerned government department to reconsider intellectual
property (IP) provisions it had earlier rejected.

What is at stake? India became the 'pharmacy of the developing world'
because its generic manufacturers are able to produce medicines that are
patented elsewhere. This has made it a safe haven for affordable medicines.
Medecins Sans Frontieres now purchases more than 80% of the medicines it
uses to treat 1,60,000 people living with HIV/AIDS around the world from
producers in India. But this safe haven has been under constant attack.

Six years ago, the first attack came when India was obliged under
international trade rules to introduce patents on medicines. Already,
patents have been granted on cancer, AIDS and hepatitis medicines. But
crucially, India's parliamentarians sought to balance patents with public
health, and designed a strict patent law that would stand up to trade rules
and protect access to affordable generic medicines.

One core provision of the law stops pharmaceutical companies from abusing
the patents system. Section 3d says no patent shall be granted for a minor
change to an existing medicine, if it shows no significant therapeutic
efficacy over one which already exists. This prevents "evergreening", when
companies seek monopolies to block out generic competition for as long as
possible, simply by making minor changes to a drug.

This has irked multinational pharmaceutical companies, which launched a
second attack on the pharmacy of the developing world. As patent
applications for several big-ticket drugs - oseltamivir for avian and swine
flu, imatinib for leukaemia and, very recently, lopinavir/ritonavir and
atazanavir for AIDS - failed to pass the patentability test in India,
companies sought to overturn the law, or empty it of any substance.
Novartis notoriously took the government of India to court in 2006, but
lost. Other companies like Bayer have taken a stab, but have yet to
succeed.

Enter the free trade agreement negotiations, as the European trade agenda
becomes the latest mouthpiece for the multinational pharmaceutical
companies. Until now, much of the debate on generic production in India has
focussed on patents. Now, the EU has changed track and is pushing hard for
India to sign up to another means of blocking off generic production: data
exclusivity.

With data exclusivity, India would be agreeing to grant a period of
exclusivity over the clinical trial data submitted by a pharmaceutical
company. This in turn would prevent the Drugs Controller General of India -
the body responsible for approving medicines for market - from registering
a generic medicine until that time was over. The multinational
pharmaceutical industry has asked for that time to be 10 years.

Data exclusivity is a backdoor to monopoly protection. It also sweeps away
the attempts by India's parliamentarians to balance health and profits. It
makes a mockery of India's patent offices' work to apply rigorous standards
and ensure only innovative medicines are granted a monopoly. Now, a
pharmaceutical company would merely have to submit clinical trial data to
obtain several years of monopoly, whether the drug was patented or not,
whether it was old or new, whether it showed inventive step or not, or gave
added therapeutic benefits or not.

The effect on access to affordable medicines is clear. India can learn from
the countries that have preceded it down this path. Jordan brought in data
exclusivity as part of a trade deal with the US. A study by Oxfam found
that of 103 medicines registered and launched since 2001 that had no patent
protection in Jordan, at least 79% had no competition from a generic
equivalent as a consequence of data exclusivity. The study also found that
prices of these medicines under data exclusivity were up to 800% higher
than in neighbouring Egypt.

India should not repeat others' mistakes, or the effect would be felt far
beyond India's borders. The country is the source of the vast majority of
drugs used to treat AIDS in developing countries. Affordable medicines
produced in India have played a major part in reaching the more than five
million people receiving HIV/AIDS treatment across the developing world
today.

In 2000, treating one HIV positive person for a year cost more than Rs
4,00,000. Thanks to competition among generics from India, this same
treatment today costs Rs 3,000. Any measure in the free trade agreement
that would have the effect of blocking competition would effectively be
turning the clock back on access to medicines. India needs to stand strong
and resist European demands.

The writer is international president, Medecins Sans Frontieres





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