PRIVATE PATENTS AND PUBLIC HEALTH
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• For more information, see Chapter 3, “The practical application of<br />
the Doha Declaration”<br />
Some companies also engaged in voluntary licensing of ARV patents,<br />
sometimes in response to non-voluntary measures by governments.<br />
Licences, whether voluntary or compulsory, allow for the manufacture<br />
and supply of generic medicines, even where a patent is otherwise in<br />
force.<br />
In 2010, UNITAID established the Medicines Patent Pool (MPP) for<br />
HIV medicines to ensure licences related to patents needed to produce<br />
WHO-recommended ARVs were available to generic producers. This<br />
created a predictable system of licences with terms and conditions<br />
formulated to serve public health.<br />
• For more on the MPP, see Chapter 3, “Medicines Patent Pool”<br />
While the fight against HIV is not yet over, huge strides have been<br />
made and continue to be made in scaling up access to life-saving ARVs.<br />
The critical question now is whether the HIV story is one that will repeat<br />
for other disease areas. Highly-priced medicines for hepatitis C and some<br />
cancers have sparked debates reminiscent of those around HIV in the late<br />
1990s. But the policy space that allowed the original HIV treatment<br />
scale-up is increasingly closing. At the same time, new issues in patents<br />
and access to medicines are emerging.<br />
INTRODUCTION<br />
• For more information, see Chapter 4, “Trade agreements closing in<br />
on TRIPS flexibilities” and Chapter 5, “Pharmaceutical innovation<br />
and access”<br />
But first, we will take a look at the details of that policy space, starting<br />
with the agreement that began it all, TRIPS.<br />
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