This is from
www.msrc.co.uk Pharmaceutical giant Sanofi withdraws (campath I think)
existing treatment to boost profits with rebranded Lemtrada.
A pharmaceutical company stands accused of putting profit before patients after withdrawing a drug used in the treatment of a chronic debilitating disease — ahead of relaunching it at a price predicted to be up to 20 times higher.
Three of Britain's leading neurologists have written to the Health Secretary, Jeremy Hunt, to protest at Genzyme, part of the multinational drug company Sanofi, halting supplies of the drug
alemtuzumab for multiple sclerosis.
The drug is currently licensed for the treatment of leukaemia. But it has been known for 20 years also to be effective in MS patients suffering from an aggressive form of the disease.
Neurologists have used the drug in these patients
"off label" — prescribing it on their own initiative even though it was not licensed for multiple sclerosis — following encouraging results from a large placebo-controlled trial published in the
New England Journal of Medicine in 1998. Alemtuzumab, which is given in two courses a year apart, costs markedly less than other drugs for multiple sclerosis to which it is thought to be superior — around ?2,500.
Genzyme has now applied for a licence for the drug in multiple sclerosis to regulators in Europe and the US and is expected to relaunch it under the trade name, Lemtrada, at what could be many times its current price. In the meantime the company has withdrawn the drug from MS patients' off-label treatment, pending the granting of the licence, on the grounds that
"any adverse event outside a clinical trial "026 may complicate the regulatory process".In the neurologists' letter to the Health Secretary, professors Neil Scolding of the University of Bristol, Neil Robertson of the University Hospital of Wales and John Zajicek of the University of Plymouth say that Genzyme's decision has
"serious implications for vulnerable UK patients with MS". They say patients who have already started treatment will
"not be able to get their vital second course", and new patients may
"miss their window of therapeutic opportunity" putting them at risk of "progressive, severe disability".When licensed, they say, the drug's price is expected to be
"15 to 20 times greater", and its withdrawal sets an
"inappropriate precedent". They add:
"It shows little regard for patients whose opportunity to alter the course of their disease is time-limited, and may represent an over-enthusiastic attempt by the parent company to profit from the current situation."Professor Zajicek said he had personally treated about 150 patients with the drug, and 400 to 500 had received it across the UK.
"Many of us think it is the best drug for patients with aggressive MS in the early stages of the disease. It's the greedy behaviour of the drug company that upsets me. They are just trying to rebrand it and put the price up. It is morally corrupt."A spokesperson for Genzyme said:
"Our goal is to ensure that Lemtrada is approved by regulatory authorities and made available to multiple sclerosis patients as quickly as possible. Until approved risk-management programmes are established, the use of Lemtrada for MS should occur only in clinical trials.