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Recruiting Phase 2 Interventional

A Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Standard of Care in Participants With Relapsed-Refractory Multiple Myeloma (RRMM)

ClinicalTrials.gov ID: NCT07227311

Public ClinicalTrials.gov record NCT07227311. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 11, 2026, 3:59 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Open Label, Non-randomized Study to Evaluate the Efficacy and Safety of Extended Dosing of Belantamab Mafodotin in Different Combinations With Standard of Care Regimens in Participants With Relapsed-refractory Multiple Myeloma (DREAMM-15)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is for adults with multiple myeloma (a type of blood cancer) that has come back after being treated earlier or isn't responding to the current treatment. The main goal is to find out if the study drug, belantamab mafodotin, given less often (on an extended schedule) with other cancer medicines, can still treat the cancer effectively while causing fewer side effects, especially those affecting the eyes. The study will also look at how well the treatment works overall and how safe it is when administered to the participants.

Study identification

NCT ID
NCT07227311
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 14, 2026
Primary completion
Aug 29, 2030
Completion
Aug 29, 2030
Last update posted
Aug 24, 2026

2026 – 2030

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Los Alamitos California 90720 Recruiting
GSK Investigational Site Torrance California 90505 Recruiting
GSK Investigational Site Whittier California 90602 Recruiting
GSK Investigational Site Norwich Connecticut 06360 Recruiting
GSK Investigational Site Fort Myers Florida 33912 Recruiting
GSK Investigational Site Macon Georgia 31210 Recruiting
GSK Investigational Site Baton Rouge Louisiana 70809 Recruiting
GSK Investigational Site Bethesda Maryland 20817 Recruiting
GSK Investigational Site Bridgeton Missouri 63044 Recruiting
GSK Investigational Site Springfield Missouri 65807 Recruiting
GSK Investigational Site Farmington New Mexico 87401 Recruiting
GSK Investigational Site Nashville Tennessee 37203 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07227311, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 24, 2026 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07227311 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →