SNP Government to Increase Access to Rare Conditions Medication

20 Jun 2018

As the SNP Government prepares to introduce a new definition of 'ultra-orphan medicines' that can treat very rare conditions affecting fewer than 1 in 50,000 people, patients across North Ayrshire and Scotland with very rare diseases should get faster access to new treatments.

 

The new definition allows the Scottish Medicines Consortium (SMC) the ability to treat some medicines for rare orphan diseases as ultra-orphan medicines.

 

If the medicine meets the new definition of an ultra-orphan medicine and the SMC consider it clinically effective, then it will be made available on the NHS for at least three years while information on its effectiveness is gathered. After this, the SMC will then review the evidence and may make a final decision on its routine use in NHS Scotland.

 

In addition, medicines that fall under the new definition and which have been recently reviewed by the SMC but not recommended for routine use, will be admitted to the new pathway.

 

Health Secretary Shona Robison said:

 

“Patients with the rarest of conditions are often children and treatment choice can be limited, so we are acting to make access to specialised medicines easier across the NHS.

 

“Changes introduced this month through the new Peer Approved Clinical System Tier Two already give doctors the right to seek access to licensed treatments not generally available in the NHS in Scotland. 

 

“These new rules for medicines that can treat those with the rarest of diseases will give faster access to new treatments. The process has been designed to be consistent and quick to implement for patients, and it will strengthen Scotland’s reputation as an international life sciences hub.

 

“Given ultra-orphan drugs are often very expensive, it is also vital that pharmaceutical companies play their part and bring a fair price, first time, to the process.”

 

Kenneth Gibson added:

 

“I am delighted that the SNP Government is following the expert recommendations given by Dr Brian Montgomery in his Review of Access to New Medicines by developing an alternative assessment pathway for ultra-orphan medicines.

 

“I look forward to patients benefitting from this increased access to the medication they need, managing rare and often very complex conditions.

 

“We should still do our best to help patients manage rare illnesses and this is a great step forward in helping to achieve that.”

 

The changes will come into effect from 01 October 2018.

 

ENDS

 

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