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Clinical trialNCT07224672RecruitingPhase 2Interventional

A Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Cyclophosphamide, Bortezomib, and Dexamethasone in Adult Participants With Newly Diagnosed Amyloid Light Chain (AL) Amyloidosis

SponsorGlaxoSmithKlineEnrollment60Amyloidosis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The study aims to evaluate the efficacy and safety of belantamab mafodotin in combination with cyclophosphamide, bortezomib, and dexamethasone in adult participants with newly diagnosed (ND) AL amyloidosis .

Investigators

No overall officials are registered on this study record. Site-level investigators, where published, appear with their sites below. Why? →

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Gsk Investigational Site

    Westmead, New South Wales, Australia

    Fiona Kwok
    Recruiting
  • Gsk Investigational Site

    Woolloongabba, Queensland, Australia

    Nirija Anderson
    Recruiting
  • Gsk Investigational Site

    Box Hill, Victoria, Australia

    Brendan Wisniowski
    Recruiting
  • Gsk Investigational Site

    Frankston, Victoria, Australia

    Patricia Walker
    Recruiting
United States
  • Gsk Investigational Site

    Rochester, Minnesota, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
24 Jun 2026
Primary completion
12 Jan 2033
Completion
12 Jan 2033
Last update posted
17 Jul 2026
Registered enrollment
60
Registry id
NCT07224672

Cross-registrations

EU-CTR / CTIS (EudraCT)2025-522803-60

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.