Michael Healy-Rae (Kerry, Independent)
Link to this: Individually | In context | Oireachtas source

207. To ask the Minister for Health his views on a matter (details supplied) regarding the drug Kalydeco; and if he will make a statement on the matter. [35543/16]

Brendan Griffin (Kerry, Fine Gael)
Link to this: Individually | In context | Oireachtas source

211. To ask the Minister for Health if he will address a matter (details supplied) regarding the drug Kalydeco; and if he will make a statement on the matter. [35559/16]

John Brassil (Kerry, Fianna Fail)
Link to this: Individually | In context | Oireachtas source

213. To ask the Minister for Health if he will allow the drug Kalydeco to be available to a person (details supplied); the reason this drug is not available for children aged two to five years of age at the same agreed price as it is available to the over six age group; and if he will make a statement on the matter. [35573/16]

Simon Harris (Wicklow, Fine Gael)
Link to this: Individually | In context | Oireachtas source

I propose to take Questions Nos. 207, 211 and 213 together.

The HSE has statutory responsibility for decisions on pricing and reimbursement of medicines under the community drugs schemes, in accordance with the Health (Pricing and Supply of Medical Goods) Act 2013.

In line with the 2013 Act, if a Company would like a medicine to be reimbursed by the HSE pursuant to the Community Drug Schemes or as a hospital medicine, the Company must first submit an application to the HSE to have the new medicine added to the Reimbursement List or to be priced as a hospital medicine.

Within 180 days of receiving the application (or such longer period which may arise if further information is sought from the Company), the HSE will decide to either:

- add the medicine to the Reimbursement List/agree to reimburse it as a hospital medicine,

or,

- will refuse to reimburse the medicine.

In reaching its decision, the HSE examines all the evidence which may be relevant in its view for the decision (including the information/dossier submitted by the Company) and will take into account such expert opinions and recommendations which may have been sought by the HSE at its sole discretion (for example, from the National Centre for Pharmacoeconomics).

In considering an application, the HSE will also have regard to Part 1 and Part 3 of Schedule 3 of the 2013 Act. Part 3 requires the HSE to have regard to the following criteria:

1. the health needs of the public;

2. the cost-effectiveness of meeting health needs by supplying the item concerned rather than providing other health services;

3. the availability and suitability of items for supply or reimbursement;

4. the proposed costs, benefits and risks of the item or listed item relative to therapeutically similar items or listed items provided in other health service settings and the level of certainty in relation to the evidence of those costs, benefits and risks;

5. the potential or actual budget impact of the item or listed item;

6. the clinical need for the item or listed item;

7. the appropriate level of clinical supervision required in relation to the item to ensure patient safety;

8. the efficacy (performance in trial), effectiveness (performance in real situations) and added therapeutic benefit against existing standards of treatment (how much better it treats a condition than existing therapies); and

9. the resources available to the HSE.

I am informed that the HSE received a request and economic dossier from the manufacturer of Ivacaftor, brand name Kalydeco, for the treatment of cystic fibrosis patients aged 2 years and older weighing less than 25kg. In March of this year the HSE asked the NCPE to carry out a health technology assessment of the applicant’s economic dossier on the cost effectiveness of this treatment.

The NCPE completed its assessment and made a recommendation in October 2016. The NCPE determined that the manufacturer failed to demonstrate cost-effectiveness of the drug for its intended cohort of patients and did not recommend that it should be reimbursed for this indication at the submitted price.

A summary of the health technology assessment has been published on the NCPE website and is available at: .

The HSE will enter into negotiations with the manufacturer in an effort to secure significant price reductions for Kalydeco.

The HSE will consider the outcome of these engagements, together with the NCPE recommendation, in making a final decision on reimbursement. This decision will be made on objective, scientific and economic grounds by the HSE in line with the 2013 Act.

As you will appreciate, I cannot comment on the case of any individual, or intervene in individual patient cases.