Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Joshua Caddy 023 8120 5537
j.caddy@soton.ac.uk


Nicole Keyworth 023 8120 3785
n.e.keyworth@soton.ac.uk


Study Location:

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Be Part of Research - Trial Details - Acalabrutinib in Combination With R-CHOP for Previously Untreated Diffuse Large B-cell Lymphoma (DLBCL)

Acalabrutinib in Combination With R-CHOP for Previously Untreated Diffuse Large B-cell Lymphoma (DLBCL)

Medical Conditions

Lymphoma
Lymphoma, B-Cell
Lymphoma, Large B-Cell, Diffuse


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


This study evaluates the addition of Acalabrutinib to current standard therapy of Rituximab, Cyclophosphamide, Doxorubicin, Vincristine and Prednisolone (R-CHOP) for patients with previously untreated CD20 positive Diffuse Large B-cell Lymphoma (DLBCL) requiring full course chemoimmunotherapy.

All patients will receive one cycle of R-CHOP. Two thirds of patients (Arm B) will go on to receive a further 5 cycles (every 21 days) of R-CHOP with Acalabrutinib. Acalabrutinib will be taken orally twice daily continuously in 21 day cycles.

One third of patients (Arm A) will continue with 5 cycles of R-CHOP.

Patients will be followed up initially for 24 months and then for disease status and survival until 114 progression events have been observed.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Oct 2021 Jan 2027

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Arm A patients will receive R-CHOP alone.

Intervention Arm Group : Arm A Control;

Intervention Type : DRUG
Intervention Description : Arm B patients will receive R-CHOP in combination with acalabrutinib.

Intervention Arm Group : Arm B Experimental;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Royal Cornwall Hospital
    Truro
  • University College London Hospital
    London
  • Southampton General Hospital
    Southampton
  • Freeman Hospital
    Newcastle
  • Nottingham City Hospital
    Nottingham
  • Addenbrooke's Hospital
    Cambridge
  • Derriford Hospital
    Plymouth
  • Leicester Royal Infirmary
    Leicester
  • Beatson West of Scotland Cancer Centre
    Glasgow
  • St James Hospital
    Leeds
  • Churchill Hospital
    Oxford
  • Queen's Hospital
    Romford
  • Ipswich Hospital
    Ipswich
  • Norfolk and Norwich University Hospital
    Norwich
  • Queen Alexandra Hospital
    Portsmouth
  • Singleton Hospital
    Swansea
  • The Christie Hospital
    Manchester
  • Royal Stoke University Hospital
    Stoke-on-Trent
  • Colchester General Hospital
    Colchester
    Essex
  • Monklands Hospital
    Airdrie
  • Torbay Hospital
    Torquay
  • Royal Derby Hospital
    Derby
  • Milton Keynes University Hospital
    Milton Keynes
  • Royal Devon and Exeter Hospital
    Exeter
  • Maidstone Hospital
    Maidstone
  • Victoria Hospital
    Blackpool
  • Royal Oldham Hospital
    Oldham
  • Queens Hospital
    Burton on Trent
  • Lewisham and Greenwich NHS Trust
    London
  • East Kent Hospitals NHS Foundation Trust
    Canterbury
    Kent
  • University Hospital Dorset NHS Foundation Trust (Bournemouth and Poole Hospitals)
    Bournemouth
  • Chase Farm and Barnet Hospitals
    London
  • Worthing and St Richards Hospitals
    Worthing


The study is sponsored by University Hospital Southampton NHS Foundation Trust and is in collaboration with AstraZeneca.




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Read full details for Trial ID: NCT04546620
Last updated 21 November 2023

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