Last updated: 03/11/2025 09:51:40
Belantamab Mafodotin plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib plus Pd in Relapsed/Refractory Multiple MyelomaDREAMM 8
EudraCT ID
EU CT Number
Not applicable
Trial status
Recruitment complete
Recruitment complete
Trial overview
Official title: A Phase III, Multicenter, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination with Pomalidomide and Dexamethasone (B-Pd) versus Pomalidomide plus Bortezomib and Dexamethasone (PVd) in Participants with Relapsed/Refractory Multiple Myeloma (DREAMM 8)
Trial description: This study will evaluate the efficacy and safety of belantamab mafodotin in combination with pomalidomide and dexamethasone (Arm A) compared with that of combination of pomalidomide, bortezomib and dexamethasone (Arm B) in participants with relapsed/refractory multiple myeloma (RRMM).
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:
Progression-Free Survival (PFS)
Timeframe: Up to approximately 174 weeks
Secondary outcomes:
Overall Survival (OS)
Timeframe: Up to approximately 473 weeks
Duration of Response (DoR)
Timeframe: Up to approximately 473 weeks
Minimal Residual Disease (MRD) negativity rate
Timeframe: Up to approximately 473 weeks
Overall Response Rate (ORR)
Timeframe: Up to approximately 473 weeks
Complete Response Rate (CRR)
Timeframe: Up to approximately 473 weeks
Percentage of participants with a confirmed Very Good Partial Response (VGPR) or better
Timeframe: Up to approximately 473 weeks
Time to Best Response (TTBR)
Timeframe: Up to approximately 473 weeks
Time to Response (TTR)
Timeframe: Up to approximately 473 weeks
Time to Progression (TTP)
Timeframe: Up to approximately 473 weeks
Progression-Free Survival 2 (PFS2)
Timeframe: Up to approximately 473 weeks
Number of participants with adverse events (AEs)
Timeframe: Up to approximately 473 weeks
Number of Participants with Clinically Significant Changes in Hematology parameters
Timeframe: Up to approximately 473 weeks
Number of Participants with Clinically Significant Changes in clinical chemistry parameters
Timeframe: Up to approximately 473 weeks
Number of participants with abnormal ocular findings on ophthalmic examination
Timeframe: Up to approximately 473 weeks
Plasma concentrations of belantamab mafodotin (ADC) at indicated time points
Timeframe: Up to approximately 473 weeks
Plasma concentrations of monomethyl auristatin-F with a cysteine linker (cys-mcMMAF) at indicated time points
Timeframe: Up to approximately 473 weeks
Area Under Plasma Concentration-time Curve (AUC) From Time 0 to the time of the last quantifiable concentration (C(tlast)) [AUC (0-last)] for Pomalidomide
Timeframe: Up to approximately 473 weeks
Area Under Plasma Concentration-time Curve (AUC) From Time 0 to End of the Dosing Interval [AUC (0-tau)] for Pomalidomide
Timeframe: Up to approximately 473 weeks
Maximum Concentration (Cmax) for Pomalidomide
Timeframe: Up to approximately 473 weeks
Time of Cmax (Tmax) for Pomalidomide
Timeframe: Up to approximately 473 weeks
Trough Concentration Prior to the Next Dose for Each Cycle (Ctrough) for Pomalidomide
Timeframe: Up to approximately 473 weeks
Last Time Point Where the Concentration is Above the Limit of Quantification (Tlast) for Pomalidomide
Timeframe: Up to approximately 473 weeks
Number of participants with positive anti-drug antibodies (ADAs) against belantamab mafodotin
Timeframe: Up to approximately 473 weeks
Titers of ADAs against belantamab mafodotin
Timeframe: Up to approximately 473 weeks
Number of Participants with Maximum post-baseline change from baseline in individual items of Patient-Reported Outcome Version of the Common Term Criteria for Adverse Events (PRO-CTCAE)
Timeframe: Up to approximately 473 weeks
Change from Baseline in health related quality of life (HRQoL) as measured by EuropeanOrganization for Research and Treatment of Cancer Quality of life Questionnaire 30-item core module (EORTC QLQ-C30)
Timeframe: Up to approximately 473 weeks
Change from Baseline in Quality of Life Questionnaire 20-item Multiple Myeloma module (QLQMY20)
Timeframe: Up to approximately 473 weeks
Change from Baseline in HRQoL as measured by EORTC IL52
Timeframe: Up to approximately 473 weeks
Interventions:
Enrollment:
302
Primary completion date:
2024-29-01
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Multiple Myeloma
Product
Not applicable
Collaborators
Not applicable
Study date(s)
October 2020 to October 2029
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
- Capable of giving signed informed consent.
- Male or female, 18 years or older.
- Active plasma cell leukemia, symptomatic amyloidosis or active polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma proliferative disorder, and skin changes (POEMS) syndrome at the time of screening.
- Prior allogeneic SCT.
Inclusion and exclusion criteria
Inclusion criteria:
- Capable of giving signed informed consent.
- Male or female, 18 years or older.
- Have a confirmed diagnosis of multiple myeloma (MM) as defined by the International Myeloma Working Group (IMWG) criteria.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
- Have been previously treated with at least 1 prior line of MM therapy including a lenalidomide-containing regimen and must have documented disease progression during or after their most recent therapy. (Participants treated with lenalidomide ≥10 mg daily for at least 2 consecutive cycles are eligible).
- Must have at least 1 aspect of measurable disease defined as one of the following; 1. Urine M-protein excretion greater than or equal to (≥)200 milligrams (mg) per 24-hour, or 2. Serum M-protein concentration ≥0.5 grams/deciliters (g/dL) (≥5.0 g/liter [L]), or 3. Serum free light chain (FLC) assay: involved FLC level ≥10 mg/dL (≥100 mg/L) and an abnormal serum free light chain ratio (less than [<]0.26 or greater than [>]1.65) only if participant has no measurable urine or serum M spike.
- Have undergone autologous stem cell transplant (ASCT) or are considered transplant ineligible. Participants with a history of ASCT are eligible for study participation provided the following eligibility criteria are met: a. ASCT was >100 days prior to the first dose of study medication. b. No active bacterial, viral, or fungal infection(s) present
- All prior treatment-related toxicities (defined by National Cancer Institute Common Terminology Criteria for Adverse Events [NCI-CTCAE] version 5.0) must be less than or equal to (≤)Grade 1 at the time of enrolment, except for alopecia.
- Adequate organ system functions as mentioned in the protocol.
- Male and female participants agree to abide by protocol-defined contraceptive requirements.
Exclusion criteria:
- Active plasma cell leukemia, symptomatic amyloidosis or active polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma proliferative disorder, and skin changes (POEMS) syndrome at the time of screening.
- Prior allogeneic SCT.
- Systemic anti-myeloma therapy (including chemotherapy and systemic steroids) within 14 days or five half-lives (whichever is shorter) preceding the first dose of study drug; prior treatment with a monoclonal antibody drug within 30 days of receiving the first dose of study drugs.
- Plasmapheresis within 7 days prior to the first dose of study drug.
- Received prior treatment with or intolerant to pomalidomide.
- Received prior Beta cell maturation antigen (BCMA) targeted therapy.
- Intolerant to bortezomib or refractory to bortezomib (for example; participant experienced progressive disease during treatment, or within 60 days of completing treatment, with a bortezomib-containing regimen of 1.3 mg/meter square [m^2] twice weekly).
- Evidence of cardiovascular risk including any of the following; 1. Evidence of current clinically significant untreated arrhythmias, including clinically significant electrocardiogram abnormalities including second degree (Mobitz type II) or third degree atrioventricular (AV) block. 2. Recent history within (3 months of screening) of myocardial infarction, acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting or bypass grafting . 3. Class III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system 4. Uncontrolled hypertension.
- Any major surgery within the last 4 weeks.
- Previous or concurrent invasive malignancy other than multiple myeloma, except: 1. The disease must be considered medically stable for at least 2 years; or 2. The participant must not be receiving active therapy, other than hormonal therapy for this disease.
- Known immediate or delayed hypersensitivity reaction or idiosyncratic reaction to belantamab mafodotin or drugs chemically related to belantamab mafodotin, or any of the components of the study treatment.
- Evidence of active mucosal or internal bleeding.
- Cirrhosis or current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice.
- Active infection requiring treatment.
- Known or active human immunodeficiency virus (HIV) infection, hepatitis B or hepatitis C will be excluded unless the protocol-defined criteria are met.
- Presence of active renal conditions (such as infection, severe renal impairment requiring dialysis or any other condition that could affect participant’s safety).
- Ongoing Grade 2 peripheral neuropathy with pain within 14 days prior to randomization or ≥Grade 3 peripheral neuropathy.
- Active or history of venous and arterial thromboembolism within the past 3 months.
- Contraindications to or unwilling to undergo protocol-required anti-thrombotic prophylaxis.
- Current corneal disease except for mild punctate keratopathy.
- Any serious and/or unstable pre-existing medical, psychiatric disorder or other conditions (including laboratory abnormalities) that could interfere with participant’s safety, obtaining informed consent or compliance to the study procedures.
- Pregnant or lactating female.
Trial location(s)
Location
GSK Investigational Site
Ft Myers, FL, United States, 33901
Status
Recruitment Complete
Location
GSK Investigational Site
Hradec Kralove, Czech Republic, 50333
Status
Recruitment Complete
Location
GSK Investigational Site
Gosford NSW, NSW, Australia, 2250
Status
Recruitment Complete
Location
GSK Investigational Site
Tucson, AZ, United States, 85712
Status
Recruitment Complete
Location
GSK Investigational Site
Pozuelo de AlarcOn Madr, Spain, 28223
Status
Recruitment Complete
Location
GSK Investigational Site
Saint Petersburg, Russia, 197341
Status
Recruitment Complete
Location
GSK Investigational Site
Boston, MA, United States, 02215
Status
Recruitment Complete
Location
GSK Investigational Site
Southampton, United Kingdom, SO16 6YD
Status
Recruitment Complete
Location
GSK Investigational Site
Takapuna Auckland, New Zealand, 622
Status
Recruitment Complete
Location
GSK Investigational Site
L'Hospitalet de Llobrega, Spain, 08908
Status
Study Complete
Location
GSK Investigational Site
Plymouth, United Kingdom, PL6 8D8
Status
Recruitment Complete
Location
GSK Investigational Site
Stoke on Trent, United Kingdom, ST4 6QG
Status
Recruitment Complete
Study documents
Protocol
Available language(s): English
Statistical analysis plan
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Recruitment complete
Actual primary completion date
2024-29-01
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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