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NCT04680468 · ClinicalTrials.gov registry record · Phase 2

Study of Belantamab Mafodotin as Pre- and Post-autologous Stem Cell Transplant and Maintenance for Multiple Myeloma

A Phase 2 study of Myeloma, sponsored by University of Pennsylvania.

Active
Registry status
Phase 2
Development phase
41
Enrollment target
1
Study location

NCT04680468 is a Phase 2 study of Myeloma that is active but no longer recruiting, run by University of Pennsylvania. The registered enrollment target is 41 participants, below the 98-participant average among 29 other Myeloma trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04680468, a Phase 2 study of Myeloma, is active but no longer recruiting, sponsored by University of Pennsylvania.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
41 participants
Enrollment target
1
Study location

Study Summary

This is a single-institution, single-arm, phase 2 study in which belantamab mafodotin (GSK2857916), an antibody-drug conjugate targeting B-cell maturation antigen (BCMA), will be administered to patients with multiple myeloma prior to and following high-dose melphalan and autologous stem cell transplantation (ASCT), in conjunction with standard lenalidomide maintenance. We hypothesize that administration of belantamab mafodotin as part of autologous stem cell transplant consolidation and maintenance will be safe, well tolerated, and efficacious in comparison to historical data.

Conditions Studied

Interventions

  • DRUG Belantamab mafodotin

Study Locations (1)

Pennsylvania

  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2021-06-02
Est. Completion 2026-07-11
Phase Phase 2

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT04680468

The ClinicalTrials.gov registry entry for NCT04680468 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 98-participant average among 29 other Myeloma trials with a reported enrollment target (58% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myeloma appearing as the primary indexed condition, and to 1 intervention - of which Belantamab mafodotin is the first listed.

NCT04680468 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT04680468 about?

NCT04680468 is a clinical study titled "Study of Belantamab Mafodotin as Pre- and Post-autologous Stem Cell Transplant and Maintenance for Multiple Myeloma". This is a single-institution, single-arm, phase 2 study in which belantamab mafodotin (GSK2857916), an antibody-drug conjugate targeting B-cell maturation antigen (BCMA), will be administered to patients with multiple myeloma prior to and following high-dose melphalan and autologous stem cell transp...

What is the current status of trial NCT04680468?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2021-06-02. Estimated completion is 2026-07-11.

What conditions does trial NCT04680468 study?

This clinical trial studies the following conditions: Myeloma.

What interventions are being tested in trial NCT04680468?

The interventions under investigation include: Belantamab mafodotin (DRUG).

Who is sponsoring clinical trial NCT04680468?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04680468 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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