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Multiple MyelomaPhase 3PrE1005NCT07285239

Belantamab Mafodotin or Daratumumab With Bortezomib, Lenalidomide and Dexamethasone for Newly Diagnosed Multiple Myeloma

A Phase 3 study testing Arm A: Belantamab Mafodotin, Arm B: Daratumumab Hyaluronidase and Bortezomib in people with Multiple Myeloma, run by PrECOG, LLC. at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Eligible participants with newly diagnosed myeloma who are not considered eligible or refuse bone marrow transplant will be enrolled. Participants will be randomized to either belantamab mafodotin or daratumumab given in combination with bortezomib, lenalidomide and dexamethasone. Read more about this study

Who is it for?
Ages 18 to 79 years
Conditions the study is for
Multiple Myeloma
What is being tested?
Arm A: Belantamab Mafodotin, Arm B: Daratumumab Hyaluronidase and Bortezomib
Could I receive a placebo?
No, everyone receives an active treatment
How many people
500 participants
Where
1 siteUnited States
Study dates
Dec 2026to Jun 2034
Phase
Phase 3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 79 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Eligibility Criteria:

  • Patient must have suspected or confirmed newly diagnosed multiple myeloma (MM) by International Myeloma Working Group (IMWG) criteria and must not have received more than one cycle of any myeloma treatment.
  • Patient must be considered ineligible for autologous stem cell transplantation by the treating physician because of their age (≥ 70 years) or aged 18 - 70 years with the presence of underlying medical conditions likely to have a negative impact on tolerability of high-dose chemotherapy with stem-cell transplantation, making them transplant ineligible, OR transplant-eligible and refusing stem-cell transplantation until first relapse or later.
  • Patient must have measurable or evaluable disease as defined by having one or more of the following, obtained within 28 days prior to randomization.
  • ≥ 1g/dL monoclonal protein (M-protein) on serum protein electrophoresis
  • Involved free light chain ≥ 10 mg/dL or ≥ 100 mg/L AND abnormal serum immunoglobulin kappa to lambda free light chain ratio (<0.26 or >1.65)
  • ≥ 200 mg/24 hours of monoclonal protein on a 24-hour urine protein electrophoresis
  • Monoclonal bone marrow plasmacytosis ≥ 30% (evaluable disease)
  • Patient must be ≥ 18 years and <80 years of age.
  • Patient must have an Eastern Cooperative Group (ECOG) Performance Status (PS) of 0-2 (PS 3 allowed if secondary to pain).
  • Patient must have IMWG Frailty Score <2.
  • Patient must have the ability to understand and willingness to sign a written informed consent document.
  • Patient must be willing to provide bone marrow (aspirate and/or biopsy) and blood samples for determination of International Myeloma Society (IMS) risk status and for research. Indeterminate patients with missing or unevaluable samples will be excluded.
  • Patient must have received no more than one cycle (28 days or less) of prior chemotherapy and no more than 160 mg of prior dexamethasone (or equivalent dose of prednisone) for treatment of symptomatic myeloma. Prior radiation therapy to symptomatic lesions is allowed provided there is no residual toxicity related to radiation and blood counts meet the study requirements. NOTE: Patients who have received prior treatment for smoldering multiple myeloma (SMM) are eligible.
  • Patient must have a Serum Protein Electrophoresis (SPEP), Urine Protein Electrophoresis (UPEP), and serum Free Light Chain (FLC) assay performed within 28 days prior to registration. In addition, a bone marrow biopsy and/or aspirate is required within 28 days prior to registration if measurable disease is only present in bone marrow. Otherwise, a bone marrow examination must have been performed within 90 days prior to registration.
  • Patient must have adequate organ function and marrow function as defined below, obtained ≤ 2 weeks prior to registration.
  • Absolute Neutrophil Count (ANC) ≥ 1000/microliter (mcL)
  • Platelets ˃75,000/mcL
  • Creatinine clearance (CrCl) ≥ 30 mL/min
  • Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤ 3x upper limit of normal (ULN)
  • Total Bilirubin ≤ 1.5x ULN or ≤ 3x ULN for patients with documented Gilbert's disease
  • Patient must agree to register to the mandatory lenalidomide (Revlimid) Risk Evaluation and Mitigation Strategy (REMS) program and be willing and able to comply with the requirements of the REMS program.
  • Patient must not be pregnant or breast-feeding due to the potential harm and teratogenic effects to an unborn fetus and possible risk for adverse events in nursing infants with the treatment regimens being used.
  • Patient must not expect to conceive or father children by using an accepted and effective method(s) of contraception or by abstaining from sexual intercourse for the duration of their participation in the study, and for 3 months after the last dose of protocol treatment.
  • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months of registration are eligible for this trial.
  • For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
  • Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
  • Patient with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, must have a clinical risk assessment of cardiac function using the New York Heart Association (NYHA) Functional Classification. To be eligible for this trial, patient must be class 2 or better.
  • Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
  • Patients must not have peripheral neuropathy ≥ Grade 2 on clinical examination or Grade 1 with pain at time of registration.
  • Patients must not have any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment according to this protocol.
  • Patient may have a history of current or previous deep vein thrombosis (DVT) or pulmonary embolism (PE) but must be willing to take some form of anti-coagulation as prophylaxis if they are not currently on full-dose anticoagulation.
  • Patients must not have any known allergies, hypersensitivity, or intolerance to corticosteroids, monoclonal antibodies or human proteins, or their excipients, or known sensitivity to mammalian-derived products.
  • Patients must not have current corneal epithelial disease except mild punctuate keratopathy.
  • Contact lenses must be avoided for participants while they are receiving belantamab mafodotin treatment unless cleared by an eye-care specialist. If cleared for use, bandaged contact lenses are specifically recommended. Contact lens use may be restarted after discontinuation of belantamab mafodotin treatment, provided the eye-care specialist confirms there are no other contraindications.
  • Patients must not have symptomatic amyloidosis or active POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma-proliferative disorder, skin changes) at the time of screening.
  • Patients must not receive any other concurrent chemotherapy, or any ancillary therapy considered investigational while on this protocol.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Michael Wright, MS contact

267-319-3910

PrE1005@precogllc.org

United States1 site, 1 recruiting
  • Gundersen Lutheran

    La Crosse, Wisconsin, 54601

    Savannah Shallue, 608-775-4113, savannah.shallue@emplifyhealth.org

    Tory Borzyskowski, 608-775-8521, tori.borzyskowski@emplifyhealth.org

    Recruiting

Other trials in United States

About this study

Official title: Randomized Phase 3 Trial of Belantamab Mafodotin or Daratumumab in Combination With Bortezomib, Lenalidomide and Dexamethasone for Newly Diagnosed Multiple Myeloma

Eligible participants with newly diagnosed myeloma who are not considered eligible or refuse bone marrow transplant will be enrolled. Participants will be randomized to either belantamab mafodotin or daratumumab given in combination with bortezomib, lenalidomide and dexamethasone. Treatment will continue until disease progression, unacceptable side effects or withdrawal of consent.

Belantamab mafodotin is a targeted cancer treatment that works against multiple myeloma cells. It combines a homing device (an antibody) with a powerful cell-killing drug (a toxin), delivering the toxin directly to cancer cells while largely sparing healthy cells.

Read more

Minimal residual disease (MRD) testing will be done on bone marrow samples obtained standardly during your treatment. MRD shows whether a very small number of cancer cells can still be detected after treatment, even if standard lab tests shows no signs of cancer.

The purpose of this study is to evaluate if belantamab mafodotin, bortezomib, lenalidomide and dexamethasone (BVRd) improves minimal residual disease (MRD) negative status and/or prolongs progression-free survival (PFS) compared with daratumumab, bortezomib, lenalidomide and dexamethasone (DVRd) in participants with newly diagnosed multiple myeloma.

Read the detailed description

This proposed Phase III multicenter, study is a randomized (1:1), open-label trial designed to show belantamab mafodotin in combination with bortezomib, lenalidomide and dexamethasone (VRd) will lead to higher minimal residual disease (MRD) negativity rate compared with daratumumab in combination with VRd newly diagnosed multiple myeloma (TI-NDMM). Patients must be ineligible for autologous stem cell transplantation because of their age (≥ 70 years) or aged 18 - 70 years with the presence of underlying medical conditions likely to have a negative impact on tolerability of high-dose chemotherapy with stem-cell transplantation, making them transplant ineligible OR transplant-eligible and refusing stem-cell transplantation until first relapse or later. In addition, progression-free survival (PFS) will also be longer.

After enrolling approximately 320 standard-risk patients (anticipated at approximately 400 total patients), the study will limit accrual to patients with high risk NDMM to allow for enrichment of this subgroup of patients.

Belantamab mafodotin is a monoclonal antibody that targets B-cell maturation antigen (BCMA), a protein expressed on the surface of plasma cells, and releases a cytotoxic agent called Monomethyl auristatin F, which destroys the plasma cells.

International Myeloma Working Group (IMWG) criteria will be used for disease response.

MRD samples will be obtained on standard of care bone marrow procedures. MRD testing will be performed on samples at time of screening, suspected complete response (sCR), after confirmed CR at applicable time points from Cycle1, Day 1 at 6, 12, 18 (optional), 24, 30 (optional) and 36 months then annually until progression. MRD testing will not be performed in real-time for this study. Bone marrow samples will also be obtained for future research at screening and time of progression.

Research peripheral blood samples will be obtained to measure levels of belantamab mafodotin in the blood, immune responses or antibodies to belantamab mafodotin for patients receiving belantamab mafodotin. In addition, research blood samples will be obtained on all patients to measure soluble B-cell maturation antigen (sBCMA) to help diagnose, monitor treatment effectiveness, and predict the prognosis of multiple myeloma.

Patient-reported outcomes will also be performed.

Being tested
Arm A: Belantamab Mafodotin, Arm B: Daratumumab Hyaluronidase, Bortezomib, Lenalidomide, Dexamethasone
Keywords
Newly Diagnosed High-Risk Multiple Myeloma, Transplant Ineligible Multiple Myeloma, High-Risk Cytogenetic Multiple Myeloma, Belantamab Mafodotin, Daratumumab-Hyaluronidase, Daratumumab, Bortezomib, Lenalidomide, Decadron, Dexamethasone
Medical subject headings
Multiple Myeloma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Arm A: Belantamab MafodotinDrug

    Also called GSK2857916, Blenrep, Belamaf

    1.9 milligram/kilogram (mg/kg) intravenous (IV) will be administered every 8 weeks for first 24 weeks (Cycles 1-3), then 1.9 mg/kg every 12 weeks (Cycles 4+) until progression, unacceptable toxicity or participant withdrawal

  • Arm B: Daratumumab HyaluronidaseDrug

    Also called DARZALEX FASPRO™

    1800 mg subcutaneous (SC) will be administered weekly from Week 1-8 (Cycles 1 and 2), every 2 weeks from Week 9-24 (Cycles 3-6), and every 4 weeks from Week 25 (Cycles 7+) onwards until progression, unacceptable toxicity or participant withdrawal

  • BortezomibDrug

    Also called Velcade®

    1.3 milligrams per square meter (mg /m²) SC on days 1, 8 and 15 of every 28 day bortezomib treatment cycle for 8 cycles

  • LenalidomideDrug

    Also called Revlimid®

    25 mg orally (PO) Days 1-21 of every 28 day lenalidomide treatment cycle.

  • DexamethasoneDrug

    Also called Decadron

    40 mg PO on Days 1, 8, 15, and 22 of each 28-day cycle (may decrease to 20 mg if >75 years old)

Study groups in NCT07285239
Study groupRoleWhat they receive
Arm A: Belantamab MafodotinExperimentalBelantamab mafodotin in combination with bortezomib, lenalidomide and dexamethasone (VRd) until progression, unacceptable toxicity or participant withdrawal. 1 cycle = 28 days.
Receives: Drug: Arm A: Belantamab Mafodotin; Drug: Bortezomib; Drug: Lenalidomide; Drug: Dexamethasone
Arm B:Active comparatorDaratumumab in combination with bortezomib, lenalidomide and dexamethasone (VRd) until progression, unacceptable toxicity or participant withdrawal. 1 cycle = 28 days.
Receives: Drug: Arm B: Daratumumab Hyaluronidase; Drug: Bortezomib; Drug: Lenalidomide; Drug: Dexamethasone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. MRD Negative Status

    MRD negative status, defined as achieving MRD negativity at 10-5 sensitivity threshold assessed by NGS at least once during the time of confirmed CR or better response per IMWG criteria by Independent Review Committee (IRC); MRD negativity is determined by the Adaptive Biotechnologies clonoSEQ® assay result

    Measured: Up to 86 months

  2. Progression-Free Survival (PFS)

    PFS, defined as the time from the date of randomization to the date of first documented disease progression per IMWG criteria by IRC or death from any cause in the absence of progression, whichever occurs first

    Measured: Up to 86 months

Secondary outcomes (12)
  1. Overall Survival (OS)

    OS, defined as the time from the date of randomization until the date of death due to any cause

    Measured: Up to 86 months

  2. Best Response of Complete Response (CR)

    Defined as confirmed CR or better per IMWG criteria by IRC

    Measured: Up to 86 months

  3. Best Response of Very Good Partial Response (VGPR)

    Defined as confirmed VGPR, CR or better per IMWG criteria by IRC

    Measured: Up to 86 months

  4. Overall Response Rate (ORR)

    Defined as confirmed PR, VGPR, CR or better per IMWG criteria by IRC

    Measured: Up to 86 months

  5. Duration of Response (DoR)

    DoR, defined as the time from first documented evidence of partial response (PR) or better until progression (PD) or death due to PD (among participants who achieve confirmed PR or better) by IRC

    Measured: Up to 86 months

  6. MRD Negative Status at 12-Month

    Defined as achieving MRD negativity at 10-5 sensitivity threshold assessed by NGS in participants achieving confirmed CR or better response per IMWG criteria by Independent Review Committee (IRC) after 12 (+/-3) months; MRD negativity is determined by the Adaptive Biotechnologies clonoSEQ® assay result

    Measured: Up to 86 months

  7. Sustained MRD (sMRD) Negative Status

    sMRD, defined as achieving MRD negative status at 10-5 sensitivity threshold assessed by NGS at least twice, a minimum of 1 year apart and with no MRD positive result in between, during the time of confirmed CR or better response per IMWG criteria by IRC

    Measured: Up to 86 months

  8. Adverse Events (AEs)

    Worst Grade 3 or Higher Treatment-Related Non-Hematologic and Overall Toxicity based on CTCAE v6.0

    Measured: While on study treatment and up to 70 days after the last dose of study medication

  9. AEs Leading to Dose Modifications

    AEs or Grade ≥ 2 Corneal Events Leading to Dose Modifications or Treatment Discontinuation

    Measured: While on study treatment and up to 70 days after the last dose of study medication

  10. Corneal Events

    Incidence of Grade ≥ 3 Corneal Events (Keratopathy Visual Acuity (KVA) scale)

    Measured: While on study treatment and up to 70 days after the last dose of study medication

  11. Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events (PRO-CTCAE)

    Frequency and Score of Selected PRO-CTCAE Attributes

    Measured: Up to 86 months

  12. Health-Related Quality of Life (HRQoL)

    Change from Baseline in HRQoL as Measured by European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30), European Organisation for Research and Treatment of Cancer Quality of Life Multiple Myeloma Questionnaire (EORTC QLQ-MY20), and Functional Assessment of Cancer Therapy - Multiple Myeloma (FACT MM) Subscale

    Measured: Up to 86 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Dec 2025
  2. Study startDec 2026 (estimated)
  3. Primary completionNov 2031 (estimated)
  4. Study completionJun 2034 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Open-label, randomized (1:1) to either belantamab mafodotin or daratumumab given in combination with bortezomib, lenalidomide and dexamethasone (VRd) until progression. Participants will be stratified by IMWG risk criteria (high-risk cytogenetics or standard-risk) and stem cell transplant (deferred or ineligible).
Masking
None (open label)
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07285239
Sponsor's protocol ID
PrE1005
Other IDs
GSK 300057
Acronym
PrE1005
Status last verified
Nov 2026
First submitted
9 Dec 2025
Last updated
6 Nov 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: Data is proprietary

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Arm A: Belantamab Mafodotin, Arm B: Daratumumab Hyaluronidase and Bortezomib in people with Multiple Myeloma, run by PrECOG, LLC. at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Michael Wright, MS (267-319-3910, PrE1005@precogllc.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

MRD Negative Status (time frame: Up to 86 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2026.

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