Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government what discussions they have had with the National Institute for Health and Care Excellence regarding the licensing of Amivantamab for the treatment of NHS cancer patients; and when they expect a licence to be granted.
Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)
Department officials have regular discussions with colleagues in the National Institute for Health and Care Excellence (NICE) about a range of issues, including access to new treatments for a range of diseases and conditions.
Amivantamab was granted a conditional marketing authorisation by the Medicines and Healthcare products Regulatory Agency for the treatment of adults with advanced non-small-cell lung cancer with activating EGFR exon 20 insertion mutations, after failure of platinum-based therapy, in November 2021.
The NICE makes evidence-based recommendations for the National Health Service on whether new, licensed medicines should be routinely funded by the NHS, based on an assessment of their costs and benefits. The NICE was unable to recommend amivantamab as a clinically and cost-effective use of NHS resources for treating EGFR exon 20 insertion mutation-positive advanced non-small-cell lung cancer after platinum-based chemotherapy in final guidance published in December 2022.
The NICE is planning to appraise amivantamab with lazertinib for untreated EGFR mutation-positive advanced non-small-cell lung cancer and amivantamab with carboplatin and pemetrexed for untreated EGFR exon 20 insertion mutation-positive advanced non-small-cell lung cancer, subject to a licence being granted for these indications. The NICE is expected to publish final guidance on both next year.
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government whether the Secretary of State for Health and Social Care intends to respond to the letter from Lord Rogan dated 13 October 2023 enclosing correspondence on behalf of the board of trustees of EGFR Positive UK, and if so, when.
Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)
The Department has received the noble lord’s letter of 13 October 2023 and will reply as soon as possible.
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government what discussions they have had, or are intending to have, with (1) Takeda Pharmaceuticals, and (2) EGFR Positive UK, following the withdrawal of the drug Mobocertinib from the UK market.
Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)
The Medicines and Healthcare products Regulatory Agency (MHRA) is engaging with Takeda Pharmaceuticals. This is to ensure that where appropriate, patients can have continued access to Mobocertinib following its withdrawal from the United Kingdom market.
The MHRA has not had discussions with EGFR Positive UK, but if approached would answer any questions they may have regarding the withdrawal of Mobocertinib from the UK market.
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government, further to the Written Answers by Lord Markham on 19 July (HL9282, HL9283 and HL9284), what steps they are taking to protect community pharmacies in Northern Ireland from closure in the continuing absence of a Northern Ireland Executive.
Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)
Community pharmacy is a devolved matter. A fully functioning devolved government is essential to the delivery of necessary healthcare reforms, including effective policies to protect community pharmacies. As an interim support, the Secretary of State has introduced appropriate measures to protect the delivery of all public services and has set a budget that protects spending to address the critical health pressures in Northern Ireland. This budget allocation gives the Northern Ireland Department of Health a total allocation of £7.3 billion, an increase of £20 million above 2022-23.
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government how many prescriptions were issued and filled by the NHS in each of the past five years; and what estimate they have made of the average gross profit margin for the pharmacist on each prescription.
Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)
The table below shows the total number of items dispensed in the community in England in each of the last five financial years broken down by English dispenser account type.
Dispenser Account Type | 2017/2018 | 2018/2019 | 2019/2020 | 2020/2021 | 2021/2022 |
English Appliance Contractor | 8,627,910 | 9,043,637 | 9,787,035 | 10,020,141 | 10,908,020 |
English Dispensing Doctor | 69,672,685 | 70,368,215 | 72,024,656 | 70,530,057 | 72,082,457 |
English Personal Administration | 14,829,104 | 14,606,249 | 14,468,189 | 13,180,273 | 13,231,305 |
English Pharmacy Contractor | 1,013,292,403 | 1,015,065,205 | 1,035,763,855 | 1,016,856,763 | 1,043,054,789 |
Total | 1,106,422,102 | 1,109,083,306 | 1,132,043,735 | 1,110,587,234 | 1,139,276,571 |
Source: NHS Business Services Authority
The table below shows the average medicine margin retained per item for English pharmacy contractors for the five financial years (2017/18 – 2021/22). Medicine margin being the difference between what the pharmacy pays for a medicine and what they are reimbursed by the National Health Service. These figures do not include any fees for service provision by the pharmacy paid by the NHS. Where it was measured that pharmacy contractors retained margin above or below the contractually agreed level, an adjustment would have been made through changes to Category M (part VIII of the Drug Tariff) reimbursement prices.
England only |
|
|
| Average margin per item (£) | Prescription items (m) |
2017/18 | £0.79 | 1013 |
2018/19 | £0.62 | 1015 |
2019/20 | £0.72 | 1036 |
2020/21 | £0.96 | 1017 |
2021/22 | £0.89 | 1043 |
Source: Department of Health and Social Care
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask His Majesty's Government what progress they have made towards releasing the £50 million they pledged in November 2021 to fund Motor Neurone Disease; and what are the reasons for the delay.
Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)
Funding for Motor Neurone Disease research has always been available via open competition. In 2021/22, NIHR spent £3.8 million on MND research, and UK Research and Innovation (UKRI), through the Medical Research Council (MRC), spent around £10.8 million. On 12 December 2022 the Government announced how at least £50 million of committed funds for Motor Neurone Disease (MND) research would be allocated over the next five years:
£8 million to early phase clinical research for MND via the National Institute for Health and Social Care Research (NIHR) Biomedical Research Centres.
£2 million to the MND Collaborative Partnership, for the research community to coordinate efforts, adding £1 million already contributed by government.
£12.5 million to MND research in the UK Dementia Research Institute (UKDRI), where seven of its fifty research programmes are focused on MND.
£6 million connect the UK DRI to the Francis Crick Institute Laboratory of Molecular Biology, the MND collaborative partnership, and the UK Dementias Platform.
The remainder (at least £21.5 million) is available via an NIHR and the Medical Research Council (MRC) rolling call for MND research supported by a joint Highlight Notice.
Asked by: Lord Rogan (Ulster Unionist Party - Life peer)
Question to the Department of Health and Social Care:
To ask Her Majesty's Government what discussions they are having with (1) the devolved administrations, and (2) travel companies, to ensure that the costs of COVID-19 test kits are not a prohibitive factor to families on limited incomes having a summer holiday.
Answered by Lord Bethell
Government officials attend regular meetings with their counterparts from the devolved administrations to share updates and coordinate and align on testing efforts where possible. The Government also recognises that the devolved administrations have their own testing systems and individual discussions with the travel industry on international travel.
Since requirements were introduced for international travel testing, the costs of testing have fallen significantly. The Government is committed to working with the travel industry and private testing providers to reduce the cost of travel testing whilst also ensuring travel is as safe as possible.