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NCT05064358 · ClinicalTrials.gov registry record · Phase 2

Study to Investigate Alternative Dosing Regimens of Belantamab Mafodotin in Participants With Relapsed or Refractory Multiple Myeloma

A Phase 2 study of Multiple Myeloma, sponsored by GlaxoSmithKline.

Active
Registry status
Phase 2
Development phase
177
Enrollment target
20
Study locations

NCT05064358: Active Phase 2 study of Multiple Myeloma, sponsored by GlaxoSmithKline.

NCT05064358 is a Phase 2 study of Multiple Myeloma that is active but no longer recruiting, run by GlaxoSmithKline. The registered enrollment target is 177 participants, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (68% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05064358, a Phase 2 study of Multiple Myeloma, is active but no longer recruiting, sponsored by GlaxoSmithKline.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
177 participants
Enrollment target
20
Study locations

Study Summary

This study aims to evaluate alternative dosing regimens of single-agent belantamab mafodotin in participants with relapsed or refractory multiple myeloma (RRMM) to determine if an improved overall benefit/risk profile can be achieved by modifying the belantamab mafodotin dose, schedule, or both.

Primary Outcome

The KVA scale is based on the evaluation of corneal changes using slit lamp examination. This scale provides a standardized approach for evaluating the relationship between corneal health and visual acuity. KVA scale is defined as Grade 0: No keratopathy, normal visual acuity with no corneal abnormalities; Grade 1: Mild changes to the cornea with no significant loss in visual acuity; Grade 2: Moderate corneal changes with noticeable visual acuity reduction; Grade 3: Severe corneal changes with s

Conditions Studied

Interventions

  • DRUG Belantamab mafodotin

Study Locations (20)

Other

  • GSK Investigational Site - Buenos Aires
  • GSK Investigational Site - Capital Federal
  • GSK Investigational Site - Ciudad Autonoma de Buenos Aire
  • GSK Investigational Site - Pilar
  • GSK Investigational Site - Rosario
  • GSK Investigational Site - Joinville
  • GSK Investigational Site - Porto Alegre
  • GSK Investigational Site - Rio de Janeiro
  • GSK Investigational Site - Salvador
  • GSK Investigational Site - São Paulo

Tennessee

  • GSK Investigational Site - Chattanooga
  • GSK Investigational Site - Nashville

New South Wales

  • GSK Investigational Site - Liverpool
  • GSK Investigational Site - Newcastle

Florida

  • GSK Investigational Site - West Palm Beach

Missouri

  • GSK Investigational Site - Kansas City

New York

  • GSK Investigational Site - New York

Texas

  • GSK Investigational Site - Houston

South Australia

  • GSK Investigational Site - Woodville

Trial Details

FieldValue
Enrollment Target 177 participants
Start Date 2022-03-03
Est. Completion 2026-01-30
Phase Phase 2
GlaxoSmithKline

1,345 total trials

What the registry record for NCT05064358 still lists

NCT05064358 is an interventional study that assigns participants to a tested intervention. The registered 177 participants enrollment target is mid-sized for trials with a published cap, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (68% lower).

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

NCT05064358 names 20 study sites across 9 states, led by Other, Tennessee, New South Wales.

Frequently Asked Questions

What is clinical trial NCT05064358 about?

NCT05064358 is a clinical study titled "Study to Investigate Alternative Dosing Regimens of Belantamab Mafodotin in Participants With Relapsed or Refractory Multiple Myeloma". This study aims to evaluate alternative dosing regimens of single-agent belantamab mafodotin in participants with relapsed or refractory multiple myeloma (RRMM) to determine if an improved overall benefit/risk profile can be achieved by modifying the belantamab mafodotin dose, schedule, or both.

What is the current status of trial NCT05064358?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 177 participants. The study started on 2022-03-03. Estimated completion is 2026-01-30.

What conditions does trial NCT05064358 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT05064358?

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

Who is sponsoring clinical trial NCT05064358?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05064358 being conducted?

This trial has 20 study locations across Florida, Missouri, New York, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Multiple Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05064358's enrollment target sits among peer trials

177 122nd of 438 higher than 316 of 438 other Multiple Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Multiple Myeloma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05064358, the US trial registry maintained by the National Library of Medicine. NCT05064358 (mid enrollment · wide site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.