Belantamab Mafodotin + Pd vs Bortezomib + Pd for Multiple Myeloma
(DREAMM 8 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests two different treatment combinations for people with multiple myeloma that has returned or resisted previous treatments. One group will receive belantamab mafodotin (an antibody-drug conjugate) with pomalidomide and dexamethasone, while the other will receive bortezomib with pomalidomide and dexamethasone. The trial aims to determine which combination is more effective and safer for managing this type of cancer. People previously treated for multiple myeloma, especially with lenalidomide, whose cancer has returned or not responded, might be suitable candidates for this trial. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.
Will I have to stop taking my current medications?
The trial requires that you stop taking any systemic anti-myeloma therapy, including chemotherapy and systemic steroids, within 14 days before starting the study drug. If you have been treated with a monoclonal antibody drug, you must wait 30 days before starting the study drugs.
Will I have to stop taking my current medications?
The trial requires that you stop any systemic anti-myeloma therapy, including chemotherapy and systemic steroids, at least 14 days before starting the study drug. If you have been treated with a monoclonal antibody drug, you must wait 30 days before starting the study drugs.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that the combination of belantamab mafodotin, pomalidomide, and dexamethasone has been studied for treating multiple myeloma and is generally well-tolerated. Some patients have reported common side effects like vision changes and low blood counts, but these can often be managed.
Bortezomib, another treatment in the trial, has already received FDA approval for multiple myeloma and has a known safety record. It is usually well-tolerated, though some patients may experience side effects like nausea, tiredness, and nerve pain.
Both treatments have undergone thorough research, indicating a reasonable level of safety. Participants in this trial will receive close monitoring to manage and address any side effects.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments for multiple myeloma because they bring new approaches to tackling the disease. Belantamab mafodotin is unique because it is an antibody-drug conjugate that targets the BCMA protein on myeloma cells, delivering a potent chemotherapy directly to the cancer cells. This targeted approach could lead to more effective treatment with fewer side effects compared to standard therapies like Lenalidomide. On the other hand, Bortezomib, combined with Pomalidomide and Dexamethasone, is a well-established regimen that works by inhibiting proteasomes, which are crucial for cancer cell survival. Together, these approaches offer promising options that could improve outcomes for patients with multiple myeloma.
What evidence suggests that this trial's treatments could be effective for relapsed/refractory multiple myeloma?
This trial will compare two treatment combinations for relapsed or refractory multiple myeloma. Participants in one arm will receive belantamab mafodotin with pomalidomide and dexamethasone. Studies have shown that this combination can be effective, helping nearly half of the patients by reducing cancer signs and allowing them to live for about 3.8 months without disease progression. Participants in the other arm will receive bortezomib with pomalidomide and dexamethasone, a well-known treatment combination effective in managing multiple myeloma symptoms. Both combinations aim to control the disease and improve patients' quality of life.678910
Who Is on the Research Team?
GSK Clinical Trials
Principal Investigator
GlaxoSmithKline
Are You a Good Fit for This Trial?
Adults with relapsed/refractory multiple myeloma who've had at least one prior therapy including lenalidomide, and have measurable disease. They must be in relatively good health (ECOG 0-2), possibly post-autologous stem cell transplant, and not have severe ongoing side effects from previous treatments. Excluded are those with certain infections, unstable liver or kidney conditions, recent heart issues or thromboembolism, active bleeding disorders, other cancers unless stable for 2 years, hypersensitivity to trial drugs or their components.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either belantamab mafodotin in combination with pomalidomide and dexamethasone or pomalidomide, bortezomib, and dexamethasone
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Belantamab mafodotin
- Bortezomib
- Dexamethasone
- Pomalidomide
Belantamab mafodotin is already approved in United States, European Union for the following indications:
- Relapsed or refractory multiple myeloma (approval withdrawn)
- Relapsed or refractory multiple myeloma
Find a Clinic Near You
Who Is Running the Clinical Trial?
GlaxoSmithKline
Lead Sponsor
Dame Emma Walmsley
GlaxoSmithKline
Chief Executive Officer since 2017
MA in Classics and Modern Languages from Oxford University
Dr. Hal Barron
GlaxoSmithKline
Chief Medical Officer since 2018
MD from Harvard Medical School