Belantamab Mafodotin In Plasmablastic Lymphoma & ALK+ Large B-Cell Lymphoma

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Jacob Soumerai, MD
Study ID
NCT04676360
Phase
PHASE2
Status
Terminated

Conditions

  • Anaplastic Lymphoma Kinase Positive Large B-Cell Lymphoma
  • Refractory Plasmablastic Lymphoma
  • Relapsed Plasmablastic Lymphoma

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Belantamab Mafodotin — DRUG
    Belantamab mafodotin will be administered intravenously at calculated dose on day 1 of each 21-day cycle.

Study Details

In this research study is looking to see how safe and effective belantamab mafodotin is in relapsed or refractory plasmablastic lymphoma or ALK+ large B-cell lymphoma. * This research study involves the study drug belantamab mafodotin. * Belantamab mafodotin is an antibody-drug conjugate (ADC), which is the combination of an antibody (a protein that binds to cells) and a drug. It works by using the antibody portion to enter into the lymphoma cells, and then releasing the drug portion to kill the lymphoma cells.

Key Dates

Start date
Jul 1, 2021
Status verified
Mar 2026
Primary completion
Nov 27, 2023
Completion
Nov 26, 2024

Study Design

Enrollment
10 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: (BELANTAMAB MAFODOTIN
    * Belantamab mafodotin will be administered intravenously on day 1 of a 21-day cycle. * Treatment is intended to be administered on an outpatient basis.

Primary Outcome Measure

Overall Response Rate [ Time Frame: Measured up to 2 years ]

Locations (3)

FacilityCityStateZIPSite coordinators
Massachusetts General HospitalBostonMassachusetts02115-
Memorial Sloan Kettering Cancer CenterNew YorkNew York10065-
MD Anderson Cancer CenterHoustonTexas77030-

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