Calendar An icon of a desk calendar. Cancel An icon of a circle with a diagonal line across. Caret An icon of a block arrow pointing to the right. Email An icon of a paper envelope. Facebook An icon of the Facebook "f" mark. Google An icon of the Google "G" mark. Linked In An icon of the Linked In "in" mark. Logout An icon representing logout. Profile An icon that resembles human head and shoulders. Telephone An icon of a traditional telephone receiver. Tick An icon of a tick mark. Is Public An icon of a human eye and eyelashes. Is Not Public An icon of a human eye and eyelashes with a diagonal line through it. Pause Icon A two-lined pause icon for stopping interactions. Quote Mark A opening quote mark. Quote Mark A closing quote mark. Arrow An icon of an arrow. Folder An icon of a paper folder. Breaking An icon of an exclamation mark on a circular background. Camera An icon of a digital camera. Caret An icon of a caret arrow. Clock An icon of a clock face. Close An icon of the an X shape. Close Icon An icon used to represent where to interact to collapse or dismiss a component Comment An icon of a speech bubble. Comments An icon of a speech bubble, denoting user comments. Comments An icon of a speech bubble, denoting user comments. Ellipsis An icon of 3 horizontal dots. Envelope An icon of a paper envelope. Facebook An icon of a facebook f logo. Camera An icon of a digital camera. Home An icon of a house. Instagram An icon of the Instagram logo. LinkedIn An icon of the LinkedIn logo. Magnifying Glass An icon of a magnifying glass. Search Icon A magnifying glass icon that is used to represent the function of searching. Menu An icon of 3 horizontal lines. Hamburger Menu Icon An icon used to represent a collapsed menu. Next An icon of an arrow pointing to the right. Notice An explanation mark centred inside a circle. Previous An icon of an arrow pointing to the left. Rating An icon of a star. Tag An icon of a tag. Twitter An icon of the Twitter logo. Video Camera An icon of a video camera shape. Speech Bubble Icon A icon displaying a speech bubble WhatsApp An icon of the WhatsApp logo. Information An icon of an information logo. Plus A mathematical 'plus' symbol. Duration An icon indicating Time. Success Tick An icon of a green tick. Success Tick Timeout An icon of a greyed out success tick. Loading Spinner An icon of a loading spinner. Facebook Messenger An icon of the facebook messenger app logo. Facebook An icon of a facebook f logo. Facebook Messenger An icon of the Twitter app logo. LinkedIn An icon of the LinkedIn logo. WhatsApp Messenger An icon of the Whatsapp messenger app logo. Email An icon of an mail envelope. Copy link A decentered black square over a white square.

Six new medicines approved including first treatment for rare heart condition

A first treatment for a rare and potentially life-threatening heart condition has been approved by the Scottish Medicine Consortium (Julien Behal/PA)
A first treatment for a rare and potentially life-threatening heart condition has been approved by the Scottish Medicine Consortium (Julien Behal/PA)

Six new medicines have been approved for use in Scotland, including the first treatment for a rare “potentially life-threatening” heart condition.

The Scottish Medicines Consortium (SMC) has approved Tafamidis for the treatment of a rare heart condition called amyloidosis cardiomyopathy (ATTR-CM).

It is the first treatment to be licensed to treat wild-type or hereditary amyloidosis cardiomyopathy and Scotland is the first in the UK to make this medicine routinely available on the NHS, pharmaceutical company Pfizer said.

ATTR-CM is a rare condition where abnormal proteins called amyloid build-up in tissues around the heart.

Dr Caroline Coats, consultant cardiologist at NHS Greater Glasgow and Clyde, said: “Transthyretin amyloid cardiomyopathy is a rare, under-diagnosed and potentially life-threatening condition, for which there is a significant unmet medical need.

“This decision is a welcome step to help expand treatment options for patients.”

Joel Rose, chief executive of Cardiomyopathy UK, said: “Amyloidosis cardiomyopathy significantly impacts everyday life for an individual and progressively worsens over time.

“Therefore, we’re pleased there is now an approved treatment option for eligible patients living in Scotland which could help improve their care.”

Owen Marks, head of rare diseases, Pfizer UK, said: “This decision is an important milestone for eligible patients in Scotland, who until now have not had a specific treatment option for amyloidosis cardiomyopathy.

“We’ll continue to work to help improve the care and diagnosis of ATTR-CM in Scotland and in the rest of the UK.”

The SMC has also approved the use of selpercatinib on an interim basis to treat a rare type of non-small cell lung cancer.

It will be available to patients while further research is undertaken.

The SMC will review the evidence and make a decision on routine availability in NHS Scotland.

Durvalumab was approved for use to treat adults with advanced biliary tract cancer which is cancer of the bile ducts which carry bile from the liver and the gallbladder to the intestines, which is newly diagnosed.

Avacopan was accepted for the treatment of adults with rare conditions that can cause blood vessels to become inflamed which can restrict blood flow and cause damage to vital organs called with severe active granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA).

Bimekizumab was accepted for the treatment of adults with psoriatic arthritis, an inflammatory arthritis associated with the skin condition psoriasis.

Risankizumab was accepted for treating Crohn’s disease in patients aged 16 or older.

However, some medicines were not accepted for use.

The committee was unable to accept efgartigimod alfa for the treatment of adult patients with the muscle weakness condition generalised Myasthenia Gravis (gMG).

It was also unable to accept pegunigalsidase alfa for the treatment of Fabry Disease, a rare inherited condition that can lead to kidney failure and heart problems.

Mercaptamine was also not accepted for use in patients with nephropathic cystinosis, a rare inherited condition that can affect the kidneys.

Tom Keith-Roach, president of AstraZeneca UK, said: “I am proud that we have been able to work with our partners in Scotland to ensure that people with this rare form of cancer have access to this new treatment.

“We look forward to further collaborating with the SMC and NHS Scotland to ensure that more patients with harder to treat cancers can benefit from our innovations.”

David Brocklehurst, head of oncology at AstraZeneca UK, said: “Until now, people with advanced biliary tract cancer have had very limited treatment options.

“Durvalumab is AstraZeneca’s first treatment for patients with GI cancers, adding to our growing portfolio of medicines that aim to revolutionise cancer care in the UK.

“Durvalumab in combination with chemotherapy has shown a clinically meaningful overall survival benefit for these patients and we will now work with the Scottish NHS and clinicians to ensure that as many patients can benefit as possible.”

SMC chairman Dr Scott Muir said: “We are very pleased to be able to accept six new medicines for use by NHS Scotland for a range of serious and disabling conditions.

“The early data for selpercatinib in a form of lung cancer is very promising. There will be a further review of updated evidence to ensure that this treatment offers what is expected in terms of clinical outcomes and good value for patients in NHS Scotland.

“Tafamidis is the first treatment to be licensed for transthyretin amyloidosis cardiomyopathy. The company presented data that suggested there would be improvements in mortality and fewer hospitalisations for patients with this terrible condition.

“From the evidence given by patients and clinicians, we know that advanced biliary tract cancer has a very poor prognosis. Adding durvalumab to current treatment may increase survival for some patients, so we know this decision will be welcomed.

“The evidence for the medicines we were unable to accept was not strong enough to satisfy the committee. We would welcome resubmissions for them once the companies have had an opportunity to address the key clinical and cost-effectiveness uncertainties highlighted.”