The UK MS Society has posted the following on its website:
Further evidence needed after disappointing Aimspro trial results, say neurologists
The results from the recently completed small study of Aimspro (goat serum) in optic neuritis (a common symptom or model for MS) were presented at a scientific meeting last week. They make it clear that the main measures used to evaluate its effect were negative. Tertiary outcomes, while not showing a benefit when compared to placebo, showed some interesting results.
A spokesman for the MS Society said, "We note that this is the first time clinical trial data involving Aimspro has been formally presented to the medical community. In the light of this new information, we want to highlight how important it is that research findings are responsibly disseminated and the need for peer-reviewed, published research information. Reports in the media can sometimes be limited or exaggerated and may lead to disappointment. The Society awaits publication of the results of this clinical trial."
By coincidence, I met someone yesterday who has been given Aimspro for a nerve condition. She said that she had seen no improvement in her condition.
I think we all need to be very wary of the likely effectiveness of this product. How many people have experienced improvements? / how long did they last? / how many saw no improvement? The data to date has been patchy to say the least.
No proper trails have been completed and all we have is claims of dramatic recoveries but with no / little evidence.