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Real-World Analysis of Belantamab Mafodotin Care Patterns in Patients With Relapsed and/or Refractory Multiple Myeloma

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Duke University

Status

Completed

Conditions

Multiple Myeloma

Treatments

Drug: Blenrep

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT05986682
218855 (Other Grant/Funding Number)
Pro00110976

Details and patient eligibility

About

The purpose of this study is to describe the real-world use of Belantamab Mafodotin - blmf (BLENREP) and associated patterns of care, including dosing and dose modification, eye care specialist visits, associated healthcare utilization, and clinical outcomes in patients with relapsed and/or refractory multiple myeloma (RRMM) seen in the Duke Cancer Institute (DCI) clinics.

Enrollment

30 patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years of age as of start of treatment with BLENREP
  • Patients with a corresponding diagnosis code consistent with multiple myeloma seen at Duke.
  • Patients with a record of starting treatment with BLENREP for RRMM between August 5, 2020 and November 22, 2022.
  • Patients having healthcare encounters at Duke Cancer Institute (DCI) for at least 1-month after start of Blenrep treatment.

Exclusion criteria

  • Patients who were included in any clinical trial for BLENREP including expanded access clinical trials
  • Age > 89 years of age as of start of index therapy

Trial design

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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