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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:

EU GSK Clinical Trials Call Center +44 (0) 20 89904466
GSKClinicalSupportHD@gsk.com


US GSK Clinical Trials Call Center 877-379-3718
GSKClinicalSupportHD@gsk.com


Study Location:

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Be Part of Research - Trial Details - Belantamab Mafodotin Plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib Plus Pd in Relapsed/Refractory Multiple Myeloma

Belantamab Mafodotin Plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib Plus Pd in Relapsed/Refractory Multiple Myeloma

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Multiple Myeloma
Neoplasms, Plasma Cell


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 will evaluate the efficacy and safety of belantamab mafodotin in combination with pomalidomide and dexamethasone (Arm A) compared with that of combination of pomalidomide, bortezomib and dexamethasone (Arm B) in participants with relapsed/refractory multiple myeloma (RRMM).

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 2020 Jan 2024

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Humanized anti-B-cell maturation antigen (BCMA) antibody/drug conjugate will be administered.

Intervention Arm Group : Arm A: Belantamab mafodotin plus Pomalidomide and Dexamethasone;

Intervention Type : DRUG
Intervention Description : Immunomodulatory drug (IMiD) will be administered.

Intervention Arm Group : Arm A: Belantamab mafodotin plus Pomalidomide and Dexamethasone;Arm B: Bortezomib plus Pomalidomide and Dexamethasone;

Intervention Type : DRUG
Intervention Description : Synthetic glucocorticoid with anti-tumor activity will be administered.

Intervention Arm Group : Arm A: Belantamab mafodotin plus Pomalidomide and Dexamethasone;Arm B: Bortezomib plus Pomalidomide and Dexamethasone;

Intervention Type : DRUG
Intervention Description : Proteasome Inhibitor will be administered.

Intervention Arm Group : Arm B: Bortezomib plus Pomalidomide and Dexamethasone;



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.

  • GSK Investigational Site
    Sutton
    Surrey
    SM2 5PT
  • GSK Investigational Site
    London
    W12 0HS
  • GSK Investigational Site
    Southampton
    Hampshire
    SO16 6YD
  • GSK Investigational Site
    Stoke-on-Trent
    Staffordshire
    ST4 6QG
  • GSK Investigational Site
    Plymouth
    PL6 8D8

US GSK Clinical Trials Call Center 877-379-3718
GSKClinicalSupportHD@gsk.com


EU GSK Clinical Trials Call Center +44 (0) 20 89904466
GSKClinicalSupportHD@gsk.com



The study is sponsored by GlaxoSmithKline




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Read full details for Trial ID: NCT04484623
Last updated 24 May 2024

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