Guest guest Posted March 5, 2010 Report Share Posted March 5, 2010 Hi Dave, Good points, that is why only the Government can afford to do a large scale trial – should they wish to go down this route ie £100m (US$150m). Also, this is rapidly becoming a human rights issue so please folks, do sign the European Parliament petition which is focussing on this issue if you haven’t already. Dr Steele MBE is fully supporting the LDNNow campaign – here’s the link to the petition http://www.ipetitions.com/petition/ldnnow/ Today we are supposedly getting a more considerate and proper response from our NIHR in the UK re our application to fund further research into LDN – one mistake they made in their response was that they said ‘we are quite happy with the medications already offered to people suffering from these diseases’. Really? What about those with SPMS or PPMS where there are no options/medications available? And also for Crohns - mesalazine which causes kidney failure. Our Government are happy with that? I think their initial response left a big loophole for us to keep banging their door down – and we at LDNNow will! Just looking forward to our response from our Prime Minister! Thanks for the helpful post. Again folks, please do sign and support our petition to the European Parliament. Jayne Crocker www.LDNNow.com Important! Please sign our LDN petition to the European Parliament by clicking here tel: +44 (0) 7877 492 669 Dr Steele MBE, talking about LDN LDNNow, a patient and friend led organisation (so not a charity) with no funding and no affiliation to any company or organisation, but rather a group of concerned individuals focussed on improving the health of those who suffer from the many diseases and conditions that LDN treats. From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Sent: 05 March 2010 07:54 low dose naltrexone Subject: [low dose naltrexone] Re:PE1296, LDN Now Petition to the ish Parliament Public Petition According to the Health Committee report human trials have limited value in determining the effectiveness of drugs. This is a quote from chapter 4 of that report (The Influence of the Pharmaceutical Industry) 5 Apr 2005. Also as far as MS is concerned LDN is dose critical and therefore another problem when designing a clinical trial. 56. Human trials tend to have limited predictive value due to problems of extrapolation to routine clinical practice. Typically, only a small sample of the prospective population to be exposed to the drug can be studied in clinical trials. Furthermore, those patients who will probably be exposed to the drug if it is marketed may be excluded from clinical trials because they have multiple pathologies or take a number of different medicines. These co-morbidities and the presence of other drugs in the body might affect the drug being investigated and not allow accurate comparison with a placebo or comparator drug. May be something you can draw to the attention of the petition committee? Quote Link to comment Share on other sites More sharing options...
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