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Written Question
Clinical Trials
Thursday 23rd April 2026

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what assessment they have made of progress toward the target set in the Life Sciences Sector Plan, published on 16 July 2025, to reduce clinical trial set-up time to 150 days by March 2026.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The Government is committed to cutting the current time it takes to get a clinical trial set up, to under 150 days by March 2026, with the aim of making the United Kingdom a world leader in clinical trials.

Data published on 15 April 2026 on GOV.UK as part of the UK Clinical Research Delivery Programme’s key performance indicators report show that average set-up times for commercial interventional clinical trials have reduced from 169 days to 122 days, when comparing the same period this year to last. This is significant progress toward the Government’s target to cut clinical trials set-up times to within 150 days.

The target set in the Life Sciences Sector Plan is that by March 2026, 95% of commercial interventional trials in England deliver set up within 150 days. Data published on 15 April 2026 on GOV.UK as part of the UK Clinical Research Delivery key performance indicators report shows that 78% of commercial interventional studies starting set-up in September 2025 met the 150-day target.

Performance data against the target will be published monthly with the final view of all studies that commenced set-up by March 2026 published in October 2026.


Written Question
Advanced Therapy Medicinal Products: Clinical Trials
Thursday 23rd April 2026

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what steps they are taking to ensure that the United Kingdom remains internationally competitive in attracting cell and gene therapy trials, including CAR-T; and to ensure that patients can access innovative treatments without delay.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The Department is committed to turbocharging clinical research and delivering better patient care, to make the United Kingdom a world-leading destination for clinical research including cell and gene therapies such as CAR-T. We are working to fast-track clinical trials to drive global investment into life sciences, improve health outcomes, and accelerate the development of medicines and therapies of the future, including gene therapy treatments.

The Department funded National Institute for Health and Care Research (NIHR) funds research and research infrastructure, which supports patients and the public to participate in high-quality research, across the development pathway.

The NIHR Industry Hub, launched in October 2025, provides a single front door for companies in England, coordinating research infrastructure into one coherent, streamlined offer.

NIHR infrastructure offers innovators access to world-leading expertise, facilities, and support for the delivery of clinical trials, strengthening the UK’s position as a partner of choice for cell and gene therapy studies. The NIHR’s Biomedical Research Centres and Experimental Cancer Medicine Centres support early translational and experimental medicine studies, offering world-leading scientific expertise and clinical capability for complex, early phase, and first-in-human trials, including CAR-T. This helps de-risk development and attract cutting-edge studies to the UK.

NIHR’s Clinical Research Facilities provide specialist environments and the skilled workforce required to deliver these complex therapies safely and efficiently. To improve delivery at scale, the NIHR’s Research Delivery Network and Commercial Research Delivery Centres are established to support rapid and efficient delivery of clinical trials and provide dedicated capacity and capability across the country. This will further enhance the UKs competitiveness by improving the speed and reliability of study setup and delivery.

In addition, the NIHR supported Advanced Therapy Treatment Centres (ATTCs) play a key role in the development of advanced therapy medicinal products clinical trials. By developing national infrastructure, standardising delivery pathways, and supporting centres across a range of geographies, ATTCs help ensure that advanced therapies can be delivered beyond a small number of highly specialised sites.


Written Question
Blood Cancer: Immunotherapy
Friday 19th December 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government how many clinical trials offering CAR-T therapy for low-grade lymphoma have closed in the last three years, and what the reasons were in each case.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

Answering this question would require Medicines and Healthcare products Regulatory Agency staff to go through a vast volume of protocol documents manually. This is because the information is not held in such a way to be able to filter electronically by the requested category.

The Guide to Parliamentary Work sets out that there is an advisory cost limit known as the disproportionate cost threshold which is the level above which departments can decide not to answer a written question. The current disproportionate cost threshold is £850.

The Guide to Parliamentary Work is published online and is available on the GOV.UK website.


Written Question
Blood Cancer: Immunotherapy
Thursday 4th December 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government which specific CAR-T treatments are available for individuals with low grade lymphomas.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England funds the use of licensed medicines that have been recommended by the National Institute for Health and Care Excellence (NICE), or the off-label use of licensed indications that have been approved via the NHS England clinical policy process.

NICE has evaluated and recommended several CAR-T therapies for both high-grade and low-grade lymphomas, some of which are recommended for a period of managed access, for instance:

  • Brexucabtagene autoleucel, for relapsed or refractory mantle cell lymphoma (MA rec) and/or relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 26 years old and over (managed access);
  • Tisagenlecleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 25 years old and under;
  • Brexucabtagene autoleucel for relapsed or refractory mantle cell lymphoma (managed access) and/or relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 26 years old and over (managed access);
  • Tisagenlecleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 25 years old and under;
  • Axicabtagene ciloleucel for diffuse large B-cell lymphoma and primary mediastinal large B-cell lymphoma after two or more systemic therapies and/or relapsed or refractory diffuse large B-cell lymphoma after first-line chemoimmunotherapy;
  • Lisocabtagene maraleucel for relapsed or refractory large B-cell lymphoma after first-line chemoimmunotherapy when a stem cell transplant is suitable; and
  • Obecabtagene autoleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia and/or relapsed or refractory B-cell acute lymphoblastic leukaemia

To support implementation of NICE recommendations, NHS England sets clinical treatment criteria to ensure that treatments are made available to those intended by the NICE Guidance. Clinical input helps set the clinical and patient treatment criteria based on the NICE committee deliberations, how the treatment will be used within the treatment pathway, and the evidence base considered by NICE and the Medicines and Healthcare Products Regulatory Agency.


Written Question
Immunotherapy: Clinical Trials
Thursday 4th December 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what support they are providing to NHS Trusts to restore or replace paused CAR-T clinical trials, to prevent patients being left without viable treatment pathways.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The Department is committed to turbocharging clinical research and ensuring that all patients, including those with cancer, have access to cutting-edge clinical trials and innovative, lifesaving treatments.

Decisions about whether a specific clinical trial should be paused are the responsibility of the study sponsor and research team, who closely monitor any reported patient safety concerns and other data that could impact a decision for an individual trial to be halted.

To support National Health Service trusts to deliver clinical trials, the Department funds research and research infrastructure across England through the National Institute for Health and Care Research, which supports patients and the public to participate in high-quality research, including on CAR-T therapy.


Written Question
Immunotherapy: Clinical Trials
Thursday 4th December 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government whether they have carried out an impact assessment on the effect of halted CAR-T clinical trials, and whether they will publish that assessment.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The Department is committed to turbocharging clinical research and ensuring that all patients, including those with cancer, have access to cutting-edge clinical trials and innovative, lifesaving treatments.

The Department has not carried out an impact assessment on the effect of halted CAR-T clinical trials. This is because decisions about whether a specific clinical trial should progress or not are the responsibility of the study sponsor and research team involved, who closely monitor any reported patient safety concerns and other data that could impact this decision.


Written Question
Blood Cancer: Immunotherapy
Thursday 4th December 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what the current NHS eligibility criteria are for CAR-T therapy for both high-grade and low-grade lymphomas.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England funds the use of licensed medicines that have been recommended by the National Institute for Health and Care Excellence (NICE), or the off-label use of licensed indications that have been approved via the NHS England clinical policy process.

NICE has evaluated and recommended several CAR-T therapies for both high-grade and low-grade lymphomas, some of which are recommended for a period of managed access, for instance:

  • Brexucabtagene autoleucel, for relapsed or refractory mantle cell lymphoma (MA rec) and/or relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 26 years old and over (managed access);
  • Tisagenlecleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 25 years old and under;
  • Brexucabtagene autoleucel for relapsed or refractory mantle cell lymphoma (managed access) and/or relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 26 years old and over (managed access);
  • Tisagenlecleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia in people aged 25 years old and under;
  • Axicabtagene ciloleucel for diffuse large B-cell lymphoma and primary mediastinal large B-cell lymphoma after two or more systemic therapies and/or relapsed or refractory diffuse large B-cell lymphoma after first-line chemoimmunotherapy;
  • Lisocabtagene maraleucel for relapsed or refractory large B-cell lymphoma after first-line chemoimmunotherapy when a stem cell transplant is suitable; and
  • Obecabtagene autoleucel for relapsed or refractory B-cell acute lymphoblastic leukaemia and/or relapsed or refractory B-cell acute lymphoblastic leukaemia

To support implementation of NICE recommendations, NHS England sets clinical treatment criteria to ensure that treatments are made available to those intended by the NICE Guidance. Clinical input helps set the clinical and patient treatment criteria based on the NICE committee deliberations, how the treatment will be used within the treatment pathway, and the evidence base considered by NICE and the Medicines and Healthcare Products Regulatory Agency.


Written Question
Commission for Countering Extremism
Monday 4th August 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Home Office:

To ask His Majesty's Government whether they plan to continue the Commission for Countering Extremism and the role of the Commissioner after the term of the current post holder ends in July.

Answered by Lord Hanson of Flint - Minister of State (Home Office)

We are currently reviewing the roles and remits of various bodies to ensure our resources are best placed to meet current challenges.

As is usual when public appointments come to an end, Ministers are considering next steps and will update the house in due course.


Written Question
Radicalism
Wednesday 2nd July 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Home Office:

To ask His Majesty's Government what is their formal definition of extremism; and how they share this definition with police, local authorities, schools and others in order to measure the scale of extremism in British society and provide clarity to those bodies about their responsibilities and powers to intervene.

Answered by Lord Hanson of Flint - Minister of State (Home Office)

The current definition of extremism, which was last reviewed by the previous government in March 2024, is openly available on gov.uk. The definition is designed to support and shape policy, not data collection or operational activity.


Written Question
Genocide: Rwanda
Monday 10th February 2025

Asked by: Lord Mendelsohn (Labour - Life peer)

Question to the Home Office:

To ask His Majesty's Government what information they have about the five Rwandan genocide suspects named in an extradition judgment and currently living in the UK.

Answered by Lord Hanson of Flint - Minister of State (Home Office)

I refer Lord Mendelsohn to UIN 249920 and UIN HL787, where similar questions were posed.

The Metropolitan Police Service (MPS) War Crimes Unit is a dedicated specialist unit which investigates and prosecutes people living in the UK suspected of committing war crimes and crimes against humanity in line with universal jurisdiction and the CPS Counter Terrorism Division has the responsibility for prosecuting such crimes. Criminal investigations are an operational matter for law-enforcement agencies, and it would be inappropriate for me to comment any further.

I would invite Lord Mendelsohn to consider referring the second part of the question to the Attorney General and the Metropolitan Police for a response.