Published 20 October 2008, doi:10.1136/bmj.a2162
Cite this as: BMJ 2008;337:a2162

Letters

What happened to the polypill?

Why is there more heat than light concerning the polypill?

The first 150 words of the full text of this article appear below.

Watts’s question—why are there still so few polypill trials?—is reasonable.1

In 2001 epidemiologist Richard Peto facilitated a meeting between the World Health Organization and the Wellcome Trust to discuss development of fixed dose combination products in secondary prevention of cardiovascular disease.2 Yusuf noted the potential for a combination treatment to reduce cardiovascular risk by three quarters in the Lancet in 2002.3 Wald and Law summarised the evidence and proposed the polypill concept, including widespread use for primary prevention, in the widely cited BMJ papers in 2003.4 Yet late in 2008 there are few trials, all in early stages. How could this be?

The big issue is not the finer points of the initial target population, the pill components, or professional opinion on the right balance between the perfect and the possible. The big issue is the huge gap in funding for research and development of affordable "applied innovations." Formulation, manufacture, . . . [Full text of this article]

Anthony Rodgers, professor1, Anushka Patel, director2

1 School of Population Health, University of Auckland, PB92019, Auckland, New Zealand, 2 Cardiovascular Division, George Institute for International Health, University of Sydney, Sydney, NSW 2000, Australia

a.rodgers@auckland.ac.nz


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Relevant Article

A strategy to reduce cardiovascular disease by more than 80%
N J Wald and M R Law
BMJ 2003 326: 1419. [Abstract] [Full Text] [PDF]




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