http://www.theherald.co.uk/news/archive/29-10-19101-0-57-27.html
Oct 29th, 2001
THE first treatment for the most
devastating form of multiple sclerosis may be provided by a drug which
is undergoing three-year trials involving almost 1000 patients.
There is no treatment available for
those with primary progressive MS, who make up about 15% of all people
with the illness.
Unlike the relapsing form of MS,
characterised by episodes of illness interspersed by periods of recovery,
it causes continuous and increasingly more crippling disability.
Scotland has one of the world's worst
records for the percentage of people crippled by MS and access to treatment
of the condition has been described in the past as resembling a lottery.
Earlier this year, JK Rowling, the
author of the Harry Potter books, was reported to be outraged at the shortage
of MS nurses north of the border.
Her mother, Anne, died from the disease
in 1990, 10 years after being diagnosed with it. Rowling is now patron
of the MS Society Scotland, one of whose volunteer members said yesterday
that any advance in the treatment of any aspect of the illness was to be
welcomed.
Jan Malesa, from Kirkwall in Orkney,
whose wife, Wendy, has suffered MS for 20 years, said: "Anything that can
promote the well-being of people with MS must be looked upon positively."
The drug now being tested for primary
progressive MS is Copaxone (glatiramer acetate). It has already proved
highly effective in treating relapsing MS.
It was introduced in the UK last
December as an alternative to beta interferon drugs used to reduce the
number of relapses suffered by patients and improve their quality of life.
Nothing yet exists which can cure
any form of MS and although beta interferons can help relapsing patients
they have no effect against the primary progressive disease.
However, Copaxone has been shown
in studies on mice to slow down the rate of deterioration in progressive
MS.
The drug, which is based on three
natural amino acids, is now being given to 900 primary progressive patients
in the UK, US and France.
Three UK centres are involved in
the trial at the Institute of Neurology in London, Queen's Medical Centre
in Nottingham and the Royal Victoria Hospital in Belfast.
Dr Phil Wood, medical director at
Teva Pharmaceuticals, the makers of Copaxone, who is helping to co-ordinate
the trials, said: "In studies on mouse models, Copaxone has been shown
to be effective.
"Of course, mice are not people but
if this drug works in the way we hope, it will be extremely significant.
"It would be the only treatment shown
to bring any benefit in this very unpleasant type of MS and to offer hope
to people who now have no access to any treatment. That would be very important.
"This disease devastates lives. People
with MS deserve treatment and I think living in the UK, the fourth or fifth
most wealthy country, we surely should be able to treat them."
RAYMOND DUNCAN