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 | News: Aimspro Successful in Optic Neuritis Trials |
Certainly, good news is a pleasant change. Just a short while after mysteriously cancelling a parallel ongoing trial, Daval International has announced successful results of their Aimspro trial specifically for Optical Neuritis.
Patients with chronic optic neuritis (inflammation of the optic nerve leading to vision disruption), were given 3 subcutaneous injections over 2 weeks. Apparently the results were positive, with minimal side effects:
" The trial participants demonstrated improvement in objectively measured visual field scores over a two week course of treatment, under double blind conditions...Within one hour of injection there was a significant improvement in colour vision, and comparison of pre-treatment and follow-up data also showed significant benefit.”
However, it later qualifies the results as "tertiary outcome measures"-- which leaves one curious as to what became of the primary and secondary outcome measures? This may be a simple misinterpretation and/or oversight on our part, but it is worth exploring in the coming weeks.
Probably more interesting still is the method of action of Aimspro. They claim that the results come very quickly ("one hour"!)-- which, given experience with traditional slow-acting immuno-modulating CRABs, must point to a different action for Aimspro.
Daval's theory is that the therapy is actually two-pronged: it immediately impacts nerve conduction, which leads to the quick results, and in the longer term has an anti-inflammatory action akin to traditional modes of action. A very relevant question is whether Aimspro actually slows/halts/reverses MS damage or "merely" works around it by improving nerve conduction. The statement mentions that the patients showed significant benefit in follow-up data, but does not quantify it. Happily, there is a promise of a significant additional findings (outside of this particular trial) that are "about to be published" regarding Aimspro's application in MS.
From Daval: “These trial results are hugely significant and have wider implications for the treatment of MS. Although this was a small trial, the Oxford Neurologists have shown that a brief course of three well tolerated sub-cutaneous injections of Aimspro, can demonstrably improve the condition of MS patients. And they echo other clinical observations which show this drug is able to improve mobility, bladder control and energy levels among MS patients.”
“Aimspro has a powerful and often rapid effect, producing dramatic improvement. We believe it to be restoring conduction in nerve and muscle fibres damaged by MS and other central and peripheral nervous system disorders, probably by an effect on biological structures within nerve and muscle known as voltage gated sodium channels.There is also clinical evidence to suggest that there may also be a repair process taking place in the longer term, which may reflect the medication’s powerful anti-inflammatory properties”.
This seems quite positive and hopeful that a relatively novel approach has been seen to benefit MSers-- we are, like all of you, anxious to learn more about Aimspro and will cover the developments with diligence.
Click "read more" for the full press release...
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Full Press Release Text
SUCCESS OF OXFORD OPTIC NEURITIS TRIAL OFFERS FRESH HOPE FOR MS SUFFERERS
- Aimspro produces ‘dramatic improvement’ in eyesight of MS patients
Britain’s 80,000 Multiple Sclerosis sufferers have been given fresh hope following the success of an independent clinical trial of Aimspro.
MS patients with the condition Optic Neuritis – an inflammation of the optic nerve and one of the most common features of multiple sclerosis - were treated with Aimspro in a recent clinical trial at Oxford University and the John Radcliffe Hospital.
Patients’ vision improved significantly following treatment with Aimspro. The trial participants demonstrated improvement in objectively measured visual field scores over a two week course of treatment, under double blind conditions - and they experienced no side effects as a result of the treatment.
These highly significant improvements in the patients sight were observed after only three sub-cutaneous injections – and the possibility of a placebo effect was excluded.
This is the first time that any treatment has been shown conclusively to reduce an aspect of disability in the chronic phases of MS to this degree.
The Aimspro trial at the John Radcliffe was a randomised, double blind, placebo controlled, crossover trial, independently designed and analysed by two of Britain’s leading MS experts, Prof. Paul Matthews and Dr. Jackie Palace, and their research fellow Dr. Georgina Burke. Patients and researchers were ‘blinded’ as to whether participants were receiving Aimspro or placebo. The crossover design meant that each patient received two weeks (three injections) of medication, and two weeks of placebo, each phase separated by a ‘washout’ period.
In tertiary outcome measures, there was a significant treatment effect on visual fields in both of the assessed measures (p=0.02 for manual points score, p=0.03 for Mean Deviation score). The report also mentions that the treatment was 'well tolerated' (i.e. there were no significant side effects).
Optic neuritis is a complication of MS where discomfort behind the eye is followed by a loss of central vision (particularly colour vision) as demonstrated using visual field testing. Generally patients’ vision recovers fully or partially as an attack of MS on the optic nerve ceases, but some have their sight permanently affected. The patients in the Oxford trial had entered a chronic phase of visual loss, with little chance of significant improvement. All the trial patients have requested to remain on the therapy.
Dr Bryan Youl, a consultant in Clinical Neurophysiology at the Royal Free Hospital in London, whose own findings on the medication’s application in MS and other neurological conditions are about to be published in the UK and Australia, is hugely encouraged by the Oxford trial results.
“These trial results are hugely significant and have wider implications for the treatment of MS. Although this was a small trial, the Oxford Neurologists have shown that a brief course of three well tolerated sub-cutaneous injections of Aimspro, can demonstrably improve the condition of MS patients. And they echo other clinical observations which show this drug is able to improve mobility, bladder control and energy levels among MS patients.”
The Oxford trial confirms Dr Youl’s own findings in observational studies carried out last year in London.
He said:
“Within one hour of injection there was a significant improvement in colour vision, and comparison of pre-treatment and follow-up data also showed significant benefit.”
He added:
“Aimspro has a powerful and often rapid effect, producing dramatic improvement. We believe it to be restoring conduction in nerve and muscle fibres damaged by MS and other central and peripheral nervous system disorders, probably by an effect on biological structures within nerve and muscle known as voltage gated sodium channels.There is also clinical evidence to suggest that there may also be a repair process taking place in the longer term, which may reflect the medication’s powerful anti-inflammatory properties”.
Dr Youl is now working with UK and Australian colleagues, on confirming his early observations on the effect of Aimspro in leucodystrophies, inherited and inflammatory peripheral neuropathies, and a range of rheumatological disorders, and muscle disorders.
Dr Bryan Youl has shown that patients with long standing complications of optic neuritis can benefit from the medication, which is given as an injection under the skin, in as little as 25 minutes. Simple neurophysiological tests verified that this phenomenon results from a reversal of ‘conduction block’ in optic nerve fibres. Dr Deidre McIntosh PhD has identified molecules critical to the mechanism of action. Dr Chris Moore FRCP has confirmed neuroscientists’ expectation that modification of sodium channel triggering is critical to the process.
The Oxford/John Radcliffe team intend to publish their analysis of the trial results in a clinical scientific journal later this year.
source:http://www.davalinternational.com/markup/news-pr-mar.cfm
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Re: Aimspro Successful in Optic Neuritis Trials (Score: 1) by DasGimp on Sunday, March 27 @ 17:56:37 EST (User Info | Send a Message) | | Great News Now when can we see it tested MORE in the USA :) .Heck you have alot of us that would love any help we could get to get some semblance of a life again,..... and Dare I Say it work and livelife again ahh some more things to dream about :) |
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Re: Aimspro (Score: 1) by fryerbj on Wednesday, April 20 @ 15:41:31 EDT (User Info | Send a Message) | 18 April ‘05
4 days ago we reported that the MHRA had instructed Daval International to cease production of Aimspro. This was following a re-interpretation of the EU rules on the subject of "specials", otherwise known as the "named patient" basis for the prescription of an unlicensed drug or treatment. Proventus is not proposing or advocating any specific course of action at this stage as we were made aware 3 days ago of a series of meetings that are being held early this week to try and resolve the situation.
We are seeking very urgent clarification of the MHRA's decision and the likely consequences for the Aimspro patients, both present and prospective. We will post any outcome and its likely consequences as soon as we are made aware of one having been made.
We feel it is inappropriate to let these meetings proceed with any attempt on our part to try and influence them; however… we will certainly have no other choice than to react in some form if the outcome is such that the halt to Aimspro production is maintained.
As taken from proventus site 20/04/2005
Regards
Brian |
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Re: Aimspro (Score: 1) by fryerbj on Wednesday, April 20 @ 15:42:13 EDT (User Info | Send a Message) | 18 April ‘05
4 days ago we reported that the MHRA had instructed Daval International to cease production of Aimspro. This was following a re-interpretation of the EU rules on the subject of "specials", otherwise known as the "named patient" basis for the prescription of an unlicensed drug or treatment. Proventus is not proposing or advocating any specific course of action at this stage as we were made aware 3 days ago of a series of meetings that are being held early this week to try and resolve the situation.
We are seeking very urgent clarification of the MHRA's decision and the likely consequences for the Aimspro patients, both present and prospective. We will post any outcome and its likely consequences as soon as we are made aware of one having been made.
We feel it is inappropriate to let these meetings proceed with any attempt on our part to try and influence them; however… we will certainly have no other choice than to react in some form if the outcome is such that the halt to Aimspro production is maintained.
As taken from proventus site 20/04/2005
Regards
Brian |
- Re: Aimspro by fryerbj on Wednesday, April 27 @ 11:35:49 EDT
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