Tag Archives: flare ups

Tocizilumab

A drug launched today could ease the agony of hundreds of children suffering from severe arthritis.

At least two thirds of children taking tocizilumab have been able to return to a normal life, after many were bedridden or forced into wheelchairs by the disease.

Doctors claim the drug has transformed the outlook for victims of systemic juvenile arthritis, a severe inflammatory disease that can affect children as young as 18 months.

Around 2,500 children in Britain are currently living with the disease, which can persist into adulthood and cause significant disability.

Until now, commonly used treatments have been anti-inflammatory drugs such as corticosteroids which may cause severe side effects and often do not slow progression of the disease.

But trial results of 112 children show after just three months of treatment with tocizilumab nearly three-quarters had a 70 per cent improvement in their condition, compared with eight per cent taking a placebo, or dummy drug.

After a year two-thirds of children had a 90 per cent improvement in their symptoms.

Dr Eileen Baildam, consultant paediatric rheumatologist and triallist at Alder Hey Children’s Hospital, Liverpool, has treated 12 children with the drug and seen them all make a remarkable recovery.

She said ‘These are very sick children, the disease affects every single joint in their bodies as well as heart and lungs. They can die from heart failure and other conditions if they don’t get treated. It’s much worse than rheumatoid arthritis in adults.

Arthritis

Arthritis

‘To control flare ups we’ve had to use huge doses of steroids which have bad side effects or another drug called methotrexate, and they tend to wear off.’

Dr Baildam said the new drug, already prescribed for adults with rheumatoid arthritis where it is not controlled by other medication, is given by intravenous infusion once a month.

‘The trial results show two-thirds get a 90 per cent response, which is almost complete recovery and with few side effects.

‘But in practice every single one of my patients has gone back to a normal life, even if they have had the disease for some time. They have been able to get out of their wheelchairs, it’s fantastic’ she said.

The new drug is a laboratory-manufactured antibody that blocks the activity of interleukin 6 (IL-6), an important immune system signalling molecule that underpins many inflammatory processes.

It may be given either on its own or in combination with standard disease modifying anti-rheumatic drugs.

The treatment made by Roche is being licensed from today for use in children aged two and older.


The £9,000 annual cost of tocilizumab, also known as RoActemra, is the same as other advanced ‘biologic’ drugs already used for arthritis, but the NHS rationing body will have to decide whether it offers value for money in children.

Dr Baildam said ‘I hope and expect it will be approved and I think it should be given to children as soon as they are diagnosed to limit the disability caused by this dreadful disease.’

Professor Patricia Woo, professor of paediatric rheumatology at London’s Great Ormond Street Hospital, which also took part in the trial, said ‘Systemic juvenile arthritis can be a devastating disease.

‘It strikes often very young children, causing chronic illness, pain and disability. It is hugely encouraging to have an effective medicine now available to alleviate symptoms, control disease activity and potentially hold back the worst long-term consequences of the disease.’

Ailsa Bosworth, chief executive of the National Rheumatoid Arthritis Society (NRAS) said the treatment offered ‘a future with hope’ to affected children and their families.

‘It causes immense distress and tocilizumab provides both families and clinicians with a new and effective treatment option which is greatly welcomed.’

New Cystic Fibrosis drug

An international team co-led by scientists at Queen’s University, Belfast, has developed a new drug for Cystic Fibrosis sufferers.

The drug specifically targets the so-called Celtic gene which is common in Ireland.

But the researchers believe the breakthrough will have significant implications for all CF sufferers.

The drug should be available to patients next year. Patients take two tablets a day.

Less than a year ago, scientists were awarded £1.7m to research and develop the drug. Specialists from Europe, America and Australia were involved in the project.

They found significant improvement in lung function, quality of life and a reduction in disease flare ups for those receiving the new treatment.

Stuart Elborn from Queen’s University, Belfast, co-led the team.

Cystic Fibrosis

Cystic Fibrosis

“The development of this drug is significant because it is the first to show that treating the underlying cause of Cystic Fibrosis may have profound effects on the disease, even among people who have been living with it for decades.

“The remarkable reductions in sweat chloride observed in this study support the idea that VX-770 improves protein function thereby addressing the fundamental defect that leads to CF.”

Dr Judy Bradley, from the University of Ulster said: “This is a ground breaking treatment because it treats the basic defect caused by the gene mutation in patients.

“Correcting the cells with this mutation shows that treatments aimed at the basic mutation can work leading to improvements in lung function and symptoms.”


Dr Damien Downey, from the Belfast Health and Social Care Trust said: “The success of this study illustrates the benefits that come from collaborative work here in Northern Ireland.

“Not only will this breakthrough help patients in Ireland and the UK but it has the potential to change the lives for those with Cystic Fibrosis around the world.”

As a result of the recent work researchers from Queen’s University, University of Ulster and clinicians from Belfast Health and Social Care Trust have been selected to join the European Cystic Fibrosis Society Clinical Trials Network.

This means Cystic Fibrosis researchers in Northern Ireland will be collaborating with their European counterparts to work toward improved treatments for Cystic Fibrosis on a global level. ”

The new drug will be submitted for licensing in the Autumn of this year and is expected to be available to patients by as early as next year.