Dillon, Richard https://orcid.org/0000-0001-9333-5296
Maycock, Shanna
Jackson, Aimee
Fox, Sonia
Freeman, Sylvie
Craddock, Charles
Thomas, Catherine
Homer, Emma
Leahy, Jane
Mamwell, Anna
Potter, Nicola
Russell, Nigel
Wei, Andrew
Ommen, Hans Beier
Hemmaway, Claire
Knapper, Steve
Billingham, Lucinda
Funding for this research was provided by:
Cancer Research UK (C65869/A29806)
AbbVie
Article History
Received: 13 June 2022
Accepted: 24 October 2022
First Online: 14 November 2022
Declarations
:
: The trial will be performed in accordance with the recommendations guiding physicians in biomedical research involving human subjects, adopted by the 18<sup>th</sup> World Medical Association General Assembly, Helsinki, Finland and stated in the respective participating countries laws governing human research, and Good Clinical Practice. The protocol has been approved by the UK (London Bridge Research Ethics Committee on 28-Sep-2020), New Zealand (Northern B Health and Disability Ethics Committee on 07-Oct-2021) and Denmark (National Center for Ethics on 25-Jul-2022). Competent Authority approval was initially granted in the UK by the Medicines and Healthcare Products Regulatory Agency (MHRA) on 06-Oct-2020; the current protocol (v4.0) was approved on 25-Mar-2021, New Zealand Auckland District Health Board (ADHB) approval was granted on 11-Oct-2021, with Danish approval granted by the Danish Medicines Agency on 22-Jun-2022.All patients provide written informed consent to participate.
: Not applicable.
: CC has received research funding from AbbVie. RD received an educational to support this trial by AbbVie, who provide venetoclax free-of-charge for use within the trial. All other authors declare no competing interests.