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Speech in Commons Chamber - Thu 24 Nov 2016
Contaminated Blood and Blood Products

"On the need for some vehicle of inquiry into the background, in an intervention I pointed out that, in the Irish Republic, the right to compensation was established in 1995. There was an Act in 1997, but it was following a tribunal of inquiry that the state admitted liability, so …..."
Mark Durkan - View Speech

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Speech in Westminster Hall - Tue 18 Oct 2016
Earlier Cancer Diagnosis: NHS Finances

"Will the hon. Gentleman give way?..."
Mark Durkan - View Speech

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Speech in Westminster Hall - Tue 18 Oct 2016
Earlier Cancer Diagnosis: NHS Finances

"I commend the hon. Member for Basildon and Billericay (Mr Baron) for leading the debate and for the leadership he has provided on one-year survival rates through the APPG. Does the Minister accept the basic premise that value of life and value for money are not in competition? They are …..."
Mark Durkan - View Speech

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Written Question
Vaccination
Monday 27th June 2016

Asked by: Mark Durkan (Social Democratic & Labour Party - Foyle)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health, when the Joint Committee on Vaccination and Immunisation will next report to his Department on the cost-effectiveness framework for vaccinations.

Answered by Jane Ellison

Upon the recommendation of the Joint Committee on Vaccination and Immunisation, the Department commissioned the Cost Effectiveness Methodology for Immunisation Programmes and Procurement (CEMIPP) Review. The Government expects to receive the CEMIPP report later this summer.


Written Question
Lung Cancer: Medical Treatments
Monday 27th June 2016

Asked by: Mark Durkan (Social Democratic & Labour Party - Foyle)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health, what plans he has to make (a) Nivolumab and (b) other immuno-oncology treatments for lung cancer available on the NHS.

Answered by George Freeman

The National Institute for Health and Care Excellence (NICE) is currently carrying out technology appraisals of nivolumab for two lung cancer indications:

(i) previously treated locally advanced or metastatic non-squamous non-small cell lung cancer. The expected publication date for this final guidance is September 2016.

(ii) Previously treated locally advanced or metastatic squamous non-small-cell lung cancer after prior chemotherapy in adults. The publication date for this final guidance is to be confirmed.

The NICE is also appraising pembrolizumab for treating advanced or recurrent PD-L1 positive non-small cell lung cancer after progression with platinum-based chemotherapy [ID840]. The expected publication date for the final guidance on this appraisal is January 2017.

Commissioners are legally required to fund drugs and treatments recommended in the NICE technology appraisal guidance within three months of its final guidance being issued. In the absence of guidance from the NICE, it is for commissioners to make decisions on whether to fund new medicines based on an assessment of the available evidence.


Written Question
Nivolumab
Monday 27th June 2016

Asked by: Mark Durkan (Social Democratic & Labour Party - Foyle)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health, what assessment he has made of the effect of the time taken for NICE appraisal processes for the provision of Nivolumab on the treatment of NHS patients with non-small cell lung cancer; and if he will make a statement.

Answered by George Freeman

No such assessment has been made.

The National Institute for Health and Care Excellence (NICE) is currently carrying out technology appraisals of nivolumab for two lung cancer indications:

(i) Previously treated locally advanced or metastatic non-squamous non-small cell lung cancer. The expected publication date for this final guidance is September 2016.

(ii) Previously treated locally advanced or metastatic squamous non-small-cell lung cancer after prior chemotherapy in adults. The publication date for this final guidance is to be confirmed.

Commissioners are legally required to fund drugs and treatments recommended in NICE technology appraisal guidance within three months of its final guidance being issued. In the absence of guidance from NICE, it is for commissioners to make decisions on whether to fund new medicines based on an assessment of the available evidence.

From July 2016, the new arrangements for the Cancer Drugs Fund will ensure that the most promising and innovative medicines get to patients as quickly as possible. In particular, NICE will issue draft guidance on new cancer drugs or significant new licence indications before they have received marketing approval in the United Kingdom. Any drug that receives a positive draft recommendation would then be funded from the point of licence.


Speech in Commons Chamber - Thu 09 Jun 2016
Carers

"Just as we must not lose our recognition of people, or identify them just by their disability, the fact that they need care or the fact that they are carers, it is important that we recruit carers to contribute to thinking on public policy—and not just when it relates to …..."
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Speech in Westminster Hall - Tue 07 Jun 2016
Support for Life-shortening Conditions

"Further to that point, does the hon. Gentleman agree that, given the sensitivity of the issue, as he has laid out so well, it is terrible that the basic message to those families who have a child with a life-shortening illness is that the reason they cannot get that support …..."
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Speech in Commons Chamber - Thu 19 May 2016
Junior Doctors Contract

"I do not wish to invite the Secretary of State to provoke or pre-empt by presumption, but if the agreement changes the shape of services, it will have implications for other health professionals. Is he prepared to have the further conversations that will need to be had, and the wider …..."
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Speech in Commons Chamber - Tue 10 May 2016
Oral Answers to Questions

"6. What steps he is taking to improve the outcomes of people with rarer cancers...."
Mark Durkan - View Speech

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