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BMJ 2006;333:276 (5 August), doi:10.1136/bmj.333.7562.276-a
Zosia Kmietowicz
London
| The first 150 words of the full text of this article appear below. |
Experts have made a raft of recommendations about how early clinical studies of new drugs should be designed, to improve their safety for the people taking part.
An interim report from an expert scientific group chaired by Gordon Duff, professor of molecular medicine at Sheffield University and chairman of the government's Commission on Human Medicines, says that new high risk agents in phase I studiesthe first time drugs are tested in humansshould be given to one person at a time, with an appropriate observation time between doses. The report follows events at Northwick Park Hospital, in London, where six volunteers were left seriously ill in a trial of the drug TGN1412 after all being given the drug at the same time (BMJ 2006;332: 682
In the trial of TGN1412 the men started to develop severe reactions within a few hours of being given the drug
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