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NCT04443829Active, not recruitingPhase 1

Immunotherapy Using CAR T-cells to Target CD19 for Relapsed/Refractory CD19+ Primary CNS Lymphoma

Immunotherapy Using CAR T-cells to Target CD19 for Relapsed/Refractory CD19+ Primary Central Nervous System (CNS) Lymphoma

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

The CAROUSEL Trial is a single-centre, non-randomised, open label Phase I clinical trial of an Advanced Therapy Investigational Medicinal Product (ATIMP) in adults (age ≥16) with relapsed/refractory Primary CNS Lymphoma. The study will evaluate the feasibility of generating the ATIMP, the safety of administering CD19CAR T-cell therapy and how effectively CD19CAR T-cells engraft, expand and persist following administration in patients with relapsed/refractory primary CNS lymphoma.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
12 (estimated)
First submitted
18 Jun 2020
Start date
23 Mar 2021
Primary completion date
30 Dec 2024
Lead sponsor
University College, London
NCT number
NCT04443829

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 12
  • From 23 Mar 2021 to the primary completion date, 30 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior allogeneic haematopoietic stem cell transplant
  • Any contraindications to PD-1 antibody Pembrolizumab
  • Evidence of active pneumonitis on chest computed tomography (CT) or positron emission tomography (PET)-CT scan at screening or history of drug-induced pneumonitis, idiopathic pulmonary fibrosis, organising pneumonia (e.g. bronchiolitis obliterans), or idiopathic pneumonitis. Prior radiation pneumonitis in the radiation field (fibrosis) is allowed (if \>24 weeks since the event)
  • Theme 2 only:
    • presence of grade 3 or 4 ICANS casually related to the ATIMP following infusion of Dose 1
    • grade 1-2 neurotoxicity (if occurred) following Theme 1 dosing (Dose 1/i.v CD19CAR Tcell dose) that has not fully resolved prior to proposed administration of 2nd CD19CAR T-cell infusion (Dose /intraventricular) for theme 2
    • grade 3-4 CRS following infusion of Dose 1
    • persisting grade 2 CRS following Theme 1 dosing (Dose 1/i.v CD19CAR T-cell dose) that has not resolved to ≤ grade 1 CRS prior to proposed administration of 2nd CD19CAR Tcell infusion (Dose 2/intraventricular) for theme 2
    • pregnancy

Other illness

  • CD19 negative disease
  • Active hepatitis B, C or HIV infection
  • Pre-existing neurological disorders (other than CNS involvement of underlying haematological malignancy)
  • History of autoimmune disease (e.g. Crohn's, rheumatoid arthritis, systemic lupus) resulting in end organ injury or requiring systemic immunosuppression/systemic disease modifying agents within the last 24 months
  • Severe intercurrent infection at the time of scheduled CD19CAR T-cell infusion

Lab values

  • Bilirubin \>2 x upper limit of normal
  • Glomerular Filtration Rate (GFR) \<50ml/min
  • Known allergy to albumin or Dimethyl sulfoxide (DMSO)
  • Arrhythmias or significant cardiac disease and left ventricular ejection fraction \<40%

Other

  • Evidence of secondary CNS lymphoma
  • Oxygen saturation ≤90% on air
  • Women who are pregnant or breast feeding
  • Inability to tolerate leucapheresis
  • ECOG 3-4
  • Life expectancy \<3months
  • Requirement for supplementary oxygen or active pulmonary infiltrates at the time of scheduled CD19CAR T-cell infusion

Who the study is looking for

  • Age ≥16
  • Patients with a histologically confirmed Diffuse Large B-Cell Lymphoma (DLBCL) confined to the CNS (Primary CNS Lymphoma (PCNSL))
  • Relapsed\* or refractory CD19+ PCNSL, defined as disease progression following CR/CRu/PR, or failure to achieve PR, after one or more lines of a high-dose methotrexate-containing protocol \*Histological confirmation by re-biopsy at relapse is recommended if feasible. However, patients will be eligible without re-biopsy provided the initial diagnostic material is available and current MRI imaging features are consistent with PCNSL by neuroradiology review.
  • Measurable disease on contrast-enhanced MRI
  • Unsuitable for alternative salvage therapies as determined by their treating physician
  • Agreement to have a pregnancy test, use highly effective contraception (if applicable)
  • Written informed consent\*\* \*\* Some patients with PCNSL may be incapable of providing their own consent due to the neurological effects of their disease. In these cases a legal representative may be sought to provide consent'.

Age in the registry: 16 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University College London Hospital
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.