Phase 3 Myeloma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have relapsed or refractory multiple myeloma (meaning the cancer has come back or stopped responding to treatment) and have received at least 1 but no more than 3 previous lines of treatment, which must have included a drug called lenalidomide and at least one other specific type of treatment (either a proteasome inhibitor or an anti-CD38 antibody)
- People whose ability to carry out daily activities is reasonably well preserved, as measured by a standard scoring system called the ECOG scale (score of 2 or lower means someone can care for themselves but may not be able to do heavy physical work) (confirm with trial site)
- People whose multiple myeloma has been confirmed to be getting worse during or after their most recent treatment, based on established medical guidelines
Who may not be able to join:
- People who have previously received certain immune-based treatments that specifically target a protein called BCMA, such as CAR-T cell therapy or bispecific antibody treatments directed at BCMA — however, people who have had a BCMA-targeting antibody-drug conjugate (such as belantamab mafodotin) are not automatically excluded
- People who have been diagnosed with certain related blood or plasma cell conditions, including plasma cell leukaemia, symptomatic amyloidosis, Waldenström macroglobulinemia, or POEMS syndrome
- People whose multiple myeloma has spread to the central nervous system (the brain or spinal cord), including the membranes surrounding the brain
- People with a history of a degenerative neurological condition, a brain infection called Progressive Multifocal Leukoencephalopathy (PML), or a movement disorder affecting the central nervous system
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Clinical Trial Management, Regeneron Pharmaceuticals
Phone: 844-734-6643
Australian sites
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
3 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Occurrence of Treatment Emergent Adverse Events (TEAEs); Severity of TEAEs; Occurrence of Adverse Events of Special Interest (AESI); Severity of AESIs; Occurrence of Serious Adverse Events (SAEs); Severity of SAEs; Minimal Residual Disease (MRD)-negative Complete Response (CR); Progression-Free Survival (PFS) per IMWG response criteria as determined by BIRC
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.