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Discount wins final NICE OK for Tasigna

UK News | January 17, 2012
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Lynne Taylor

Discount wins final NICE OK for Tasigna

In final guidance, the National Institute for Health and Clinical Excellence (NICE) says that, following the offer of a discount, it is able to recommend the use of Novartis' Tasigna (nilotinib) for the treatment of chronic myeloid leukaemia (CML).

Specifically, the final guidance says that NICE recommends Tasigna for the chronic and accelerated phases of CML that is resistant or intolerant to standard-dose imatinib (Novartis' Glivec), and that it does not recommend Bristol-Myers Squibb's Sprycel (dasatinib) or high-dose Glivec for this use.

"CML is a chronic condition, meaning the drugs will be used for a long period of time and, at over £30,000 per patient per year, nilotinib is expensive. However, the manufacturer has agreed to provide it to the NHS at a discounted price. This reduction in cost enabled the independent committee to approve nilotinib for use," said Professor Carole Longson, director of the health technology evaluation centre at NICE.

Novartis, which has requested that the size of the discount should remain confidential, welcomed NICE's final backing for Tasigna, and it was described as "excellent news" by Richard Clark, professor of haematology at the Royal Liverpool University Hospital.

"This ends a period of uncertainty about whether the NHS would support [Tasgna's] costs," said Prof Clark. "This means that all patients in England and Wales who require nilotinib as a second-line treatment can receive this on the NHS. Nilotinib is already available in Scotland for such patients," he added.

Novartis Oncology says it has worked closely with the Department of Health (DH) to establish a Patient Access Scheme (PAS) for Tasigna. "Our priority is to ensure that as many patients as possible can benefit from innovative therapies, like nilotinib, which we have developed to address unmet meets in difficult-to-treat diseases," said Panos Alexakos, oncology general manager at Novartis UK & Ireland. 

"By working in partnership with the DH, we have succeeded in ensuring that patients and health services benefit from the most cost-effective option available for first- and second-line Philadelphia chromosome-positive CML," he said.

- Earlier this month, Health Secretary Andrew Lansley told Parliament that the government will establish "an effective compliance regime" to ensure that Primary Care Trusts (PCTs) make available all drugs which are recommended by NICE.

This had not been the case under the previous Labour government, but, through the compliance regime and "a new NICE collaboration imperative….we will make certain that where NICE gives a positive appraisal for medicine that it is automatically included," Mr Lansley told MPs.


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Comments 3

  1. A concerned Carer 17 Jan

    So let me see if I understand this correctly, The only CML drugs currently accessible to patients here in the UK are those supplied by Novartis.  So, whether a patient has mutations that are not addressed by either of the Novartis drugs, too bad, they cannot access them.  Whether a patient has a current heart condition which would preclude them from being on Tasigna, too bad, the patient cannot access Sprycel. (Tasigna carries a black box warning on the label in the US).



    We have learned that there is no one drug fits all, that is the reason why there are so many different drugs available- from different manufacturers.



    The price of Tasigna is obviously the same price as Imatinib 400mg once daily, otherwise the higher dose Imatinib would have also been approved.  So, this decision was based on cost alone.



    The government wins this round as you have successfully set the TKI market value to be that which is represented by the price of 400mgs of Imatinib, nothing more, but of course you would consider less.  Fair enough to say that Pharma probably does overcharge for many of these drugs.  



    However, this is a deadly war that you have started.  The only real losers will be the patients and their families.  Once they go into accelerated and blast phase there really is no hope of recovering their life.  Interestingly enough in other more forward thinking countries in the world we are starting to see patients being rescued with the newer drugs, which includes Sprycel and being able to stop the drugs all together, effectively cured.  Yet if these very same patients where here in the UK, their lives would be in grave danger.



    If you truly want to get it right for your patients, their families and the doctors who treat them, you must invite Bristol Myers Squibb back to the negotiation table.



    Novartis shouldn't climb up on their white horse so quickly.  The stead they rode in on is made up of the coffins of many patients they just consigned to their deaths.  Novartis are you really a patient centric company when you have clearly made such a strong attempt to deny doctors and patients to any other drugs than your own?  Take off the disguise, you haven't earned it.
  2. The Realist 20 Jan

    Welcome to the NHS concerned carer! Look on the bright side, at least Tasigna can finally be accessed on the NHS (about 4 years after it was first approved for use in the EU).



    Unfortunately the UK government has a finite budget and Sprycel is just too expensive. By approving Sprycel for CML patients, many other patients would miss out somewhere else.



    The reference pricing system, that would force the price down in other countries if BMS lowered it in the UK, means BMS have sacrificed the UK market (and UK patients) to keep a high price and maintain profits. Unfortunately, as always, it is the patients that suffer - but what can you do?
  3. Been There 16 Apr

    I agree with concerned carer. Hopefully a patient that has a mutation that Tasigna doesnot address but Sprycel does will be able to obtain the Sprycel . I guess you get what you pay for. Unfortunately for the Tasigna patients this is a lifetime commitment of twice a day with 6 hours of fasting. Sadly, many patients on chronic therapy get into trouble not taking their therapy due to poor adherence. I just have had two on gleevec with such an experience after over 7 yrs of once a day. Patients that fail and go to accelerated or acute.....hmm...wonder
    how much that will cost......Sometimes we fail to see the forest through the trees.

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