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High cost and poor availability of drugs mean that important clinical questions remain unanswered
| The first 150 words of the full text of this article appear below. |
In May 2004, the European Clinical Trials Directive came into force. The directive made it mandatory for all clinical drug trials to follow the good clinical practice guidance, and it fuelled existing concerns that financial and organisational constraints were making it almost impossible to conduct independent trials not funded by the drug industry. In the accompanying paper, Berendt and colleagues show that the decrease in the number of new clinical trials registered each year in Denmark began well before 2004, and the decrease was similar for independent and industry sponsored trials.1 In 2006, two years after the enforcement of the EU directive, the number of independent trials actually increased. Similar results have been reported in Sweden, Norway, and Italy.2 The consistency of these findings, despite differences in registration and classification systems, supports their validity and generalisability.
So can we feel reassured about the future of independent therapeutic research? Certainly, clinical
Paolo Bruzzi, head, director1,2
1 Clinical Epidemiology Unit, National Cancer Research Institute, 16132 Genova, Italy, 2 Department of Epidemiology and Prevention, National Cancer Research Institute
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