Cannabis-based drug is cleared for use by multiple sclerosis sufferers
Your support helps us to tell the story
From reproductive rights to climate change to Big Tech, The Independent is on the ground when the story is developing. Whether it's investigating the financials of Elon Musk's pro-Trump PAC or producing our latest documentary, 'The A Word', which shines a light on the American women fighting for reproductive rights, we know how important it is to parse out the facts from the messaging.
At such a critical moment in US history, we need reporters on the ground. Your donation allows us to keep sending journalists to speak to both sides of the story.
The Independent is trusted by Americans across the entire political spectrum. And unlike many other quality news outlets, we choose not to lock Americans out of our reporting and analysis with paywalls. We believe quality journalism should be available to everyone, paid for by those who can afford it.
Your support makes all the difference.People with multiple sclerosis can be prescribed a new cannabis-based med-icine even though it is yet to be licensed in the UK.
The Home Office has agreed to requests from doctors and patients to allow Sativex to be imported from Canada, where it has been on sale since late June.
The decision by Paul Goggins, the Home Office minister with responsibility for drugs, was made in spite of the refusal of regulators last year to award Sativex a full licence in the UK until more clinical data was available.
A statement from the drug's manufacturer, GW Pharmaceuticals, said there was scope within the Medicines Act for a drug to be prescribed and supplied in response to a specific request from a GP even if it had not yet been licensed. "The basis on which Sativex may be imported, therefore, is the clinical judgement of doctors in relation to specific, nominated patients," GW said.
Doctors will need a special Home Office licence to prescribe Sativex - an oral spray designed to relieve spasticity, or involuntary muscle contractions, in MS sufferers. Because it will remain a controlled drug, GW said that talks would take place with the Home Office during the coming weeks over how a licensing regime can be put in place.
After the Home Office agreement was made known yesterday, shares in GW rose by 20 per cent. The company also confirmed that it still intended to seek full regulatory approval for Sativex in the UK.
The company is conducting further trials and is planning to submit a fresh marketing application to the Medicines and Healthcare Products Regulatory Agency (MHRA) in 2006. Only after such an approval is granted can the product be promoted in the UK.
A spokeswoman for the Department of Health said: "Last year the MHRA refused a licence for Sativex for the treatment of patients with MS. Sativex is therefore not licensed in the UK but a clinician may prescribe the drug for unlicensed use for named patients in exceptional cases. A clinician who wishes to prescribe Sativex on the NHS will need to get the decision ratified by the appropriate NHS trust and/or primary care trust."
Join our commenting forum
Join thought-provoking conversations, follow other Independent readers and see their replies
Comments