Dáil Éireann Debate, Tuesday - 10 October 2017
284. Deputy Gerry Adams asked the Minister for Health the status for funding in respect of a drug (details supplied) used in the treatment of phenylketonuria; and if he will make a statement on the matter. [42487/17]
Amharc ar fhreagra295. Deputy Thomas Pringle asked the Minister for Health the reason Kuvan, the only drug available to those diagnosed with PKU, was refused by the HSE in view of the fact that it radically improves the quality of life for those with the condition; if he has given consideration to providing funding in order that the drug can be offered to persons here; and if he will make a statement on the matter. [42510/17]
Amharc ar fhreagra322. Deputy Seán Barrett asked the Minister for Health if the drug Kuvan will be made available for sufferers of the genetic disorder phenylketonuria (details supplied); and if he will make a statement on the matter. [42620/17]
Amharc ar fhreagraI propose to take Questions Nos. 284, 295 and 322 together.
The HSE has statutory responsibility for decisions on pricing and reimbursement of medicines under the community drug schemes, in accordance with the Health (Pricing and Supply of Medical Goods) Act 2013.
In reaching its decision, the HSE examines all the evidence which may be relevant in its view for the decision and will take into account such expert opinions and recommendations which may have been sought by the HSE, including, for example, advice from the National Centre for Pharmacoeconomics, NCPE.
Sapropterin (Kuvan) was previously considered under the national pricing and reimbursement processes in 2009. At that time, insufficient evidence was available to support the pricing and reimbursement application submitted by Merck Serono for Kuvan.
In December 2015, Merck Serono advised the HSE that the market authorisation for Kuvan was transferring to Biomarin in 2016. The HSE met with the new market authorisation holder Biomarin in May 2016 and was advised that it would be submitting a health technology assessment dossier in relation to Kuvan.
The NCPE assessment of the Biomarin dossier was completed on 15 September 2017, and the NCPE did not recommend Kuvan for reimbursement as it was not deemed cost-effective.
The HSE assessment process is ongoing, and the HSE will take into account any relevant expert advice when making its decision, in line with the Health (Pricing and Supply of Medical Goods) Act 2013.
