The Mail on Sunday

New pill treats MS ...without agony of stomach troubles

By

- Ethan Ennals

MULTIPLE sclerosis patients forced to quit vital medication due to the intolerabl­e stomach trouble it causes are to be offered a new breed of pills designed to reduce severe reactions.

The medication, taken twice a day, works just as well as previous drugs that have revolution­ised treatment of the autoimmune condition – known collective­ly as disease-modifying therapies – but without the uncomforta­ble side effects that many suffer.

Now, following authorisat­ion from Britain’s medicines watchdog, doctors hope the pill, diroximel fumarate – brand name Vumerity – could provide more sufferers the opportunit­y to control their condition.

Dr Martin Duddy, a consultant neurologis­t who treats MS patients at the Royal Victoria Hospital in Newcastle, says: ‘Disease-modifying therapies can really improve quality of life, but they often come with the trade off of some really uncomforta­ble stomach issues.

‘For many patients it can just be too much. Any new options which would allow them to continue on the therapies would be welcomed.’

More than 130,000 people in the UK suffer from multiple sclerosis, an incurable disease which develops when the immune system goes haywire, attacking the myelin sheath, the protective coating on brain and spinal-cord nerves.

This leads to symptoms such as poor mobility and numbness in the limbs, as well as mental health problems. About 85 per cent of patients have relapsing-remitting MS and can go months without symptoms, but suddenly fall ill. During relapses, the symptoms can be so severe they find it near-impossible to carry out everyday tasks.

In the past 20 years, drugs have become available that can reduce the number of relapses. These disease-modifying therapies, such as one called Tecfidera, routinely used on the NHS, can cut relapses by about 50 per cent, according to studies. However, side effects are common, with many patients experienci­ng stomach cramps, diarrhoea and nausea.

Dr Duddy said: ‘If patients come off Tecfidera or other diseasemod­ifying therapies, they will usually have to go on to less effective drugs, meaning more relapses, or stronger medication which carries a larger risk of complicati­ons.’

Vumerity contains the same active ingredient as Tecfidera to reduce inflammati­on and protect the nerve cells from the damage that causes MS symptoms. But the new drug has a different chemical structure, which means it’s better tolerated by patients.

US studies have found that patients on Vumerity see a similar reduction in relapses to those on Tecfidera, but develop significan­tly fewer stomach problems.

Dr Duddy said: ‘It appears that patients on Vumerity typically live more comfortabl­e lives. They’re obviously not completely sideeffect free – no drug is – but it appears that the stomach issues it causes are much easier to tolerate.

‘That’s not to say everyone should come off Tecfidera, but it would be a valuable option for MS patients being treated on the NHS.’

Vumerity received authorisat­ion for use in the UK by the Medicines and Healthcare Products Regulatory Agency last month. A decision on its use from NHS watchdog the National Institute for Health and Care Excellence is pending.

ONE patient who could benefit from the treatment is Harriet Betts, 33, from Southampto­n who was diagnosed with relapsing-remitting MS four years ago after she suffered partial vision loss.

Harriet, who works in a sun-bed shop, was put on Tecfidera, which led to a number of severe side effects, including painful, sun-burnlike skin flushing and constipati­on.

The mother-of-four was moved on to another disease-modifying therapy, but now has to go into hospital every six months for an infusion and is then required to rest in bed for several days to avoid any complicati­ons.

She says a new treatment that could reduce side effects caused by disease-modifying therapies would help her and others.

She adds: ‘All these drugs have horrid side effects.

‘It’s something you learn to live with because you’re hoping it’ll help your MS.

‘The thought that patients like myself could get something that doesn’t make you feel sick all the time is really positive.’

 ?? ?? HOPEFUL: Harriet Betts was diagnosed four years ago
HOPEFUL: Harriet Betts was diagnosed four years ago

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