[引用][C] Minimising risk in first-in-man trials
J Hemelaar - The Lancet, 2007 - thelancet.com
Comment www. thelancet. com Vol 369 May 5, 2007 1497 infusions would clearly have
been beneficial. The regimen was explained to volunteers as:“For practical reasons, the time …
been beneficial. The regimen was explained to volunteers as:“For practical reasons, the time …
Systematic reviews of animal experiments
P Sandercock, I Roberts - The Lancet, 2002 - thelancet.com
The axiom “before testing a new treatment in man, test it first in animals if possible” has been
part of drug development for the past 50 years or so. Testing in animal models is believed to …
part of drug development for the past 50 years or so. Testing in animal models is believed to …
Trial re-investment to build better research for better impact
TA Fox, GA Horne, C Craddock, G Cook, S O'Brien… - The Lancet, 2019 - thelancet.com
We thank the correspondents for their responses to our Comment. 1 Although randomised
controlled trials (RCTs) that are rigorously designed, conducted, and analysed provide …
controlled trials (RCTs) that are rigorously designed, conducted, and analysed provide …
[HTML][HTML] The importance of randomised vs non-randomised trials–Authors' reply
HC Gerstein, J McMurray, RR Holman - The Lancet, 2019 - thelancet.com
Although randomised controlled trials (RCTs) that are rigorously designed, conducted, and
analysed provide reliable and comprehensive information on the risks and benefits of …
analysed provide reliable and comprehensive information on the risks and benefits of …
Reporting drug safety in clinical trials: getting the emphasis right
JC Mucklow - The Lancet, 2001 - thelancet.com
The requirements for data collection during clinical trials of new drugs are rigorous.
Unexpected outcomes are as important as expected ones, and all adverse events should be …
Unexpected outcomes are as important as expected ones, and all adverse events should be …
10 years of the UK's National Institute for Health Research
J Bell - The Lancet, 2016 - thelancet.com
The revolution in molecular medicine and cell biology that occurred in the late 20th century
was a magnet for research funding and continues to advance understanding of disease. By …
was a magnet for research funding and continues to advance understanding of disease. By …
The death of academic clinical trials
AH Morice - The Lancet, 2003 - thelancet.com
The Medicines Control Agency (MCA) consultation letter MLX287 (www. mca. gov. uk),
concerning the implementation of European Union directive 2001/20/EC on good clinical …
concerning the implementation of European Union directive 2001/20/EC on good clinical …
[引用][C] The EU clinical trials directive: 3 years on
R Hoey - The Lancet, 2007 - thelancet.com
World Report clinical trials, insists that the estimate was if anything a conservative one.”
There's little doubt this has been a very salutary lesson. It is amazing how few people took …
There's little doubt this has been a very salutary lesson. It is amazing how few people took …
Drug development and clinical research in the UK
WF Crowley - The Lancet, 2007 - thelancet.com
The problem is clear: for every new drug that is approved, US $1 billion in research is spent,
10 years of development are required, and nine of every ten drugs fail. 1 With health-care …
10 years of development are required, and nine of every ten drugs fail. 1 With health-care …
Independent clinical research in Europe
G Remuzzi, A Schieppati, JP Boissel, S Garattini… - The Lancet, 2004 - thelancet.com
The selection of comparators is another crucial point in assessing the value of new drugs.
Too often, placebo is still selected as the comparator, raising doubts about the clinical …
Too often, placebo is still selected as the comparator, raising doubts about the clinical …