Phase 3 Myeloma Trial, Recruiting NCT07222761 Sponsor: Regeneron Pharmaceuticals Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT07222761
Recruiting Phase 3 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Clinical Trial Management, Regeneron Pharmaceuticals

Phone: 844-734-6643

Australian sites

Mater Misericordiae Ltd, Brisbane, Queensland
Gold Coast Hospital and Health Service, Southport, Queensland
Alfred Hospital, Melbourne, Victoria

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

Status
Recruiting
Phase
Phase 3
Sponsor
Regeneron Pharmaceuticals
Registry
ClinicalTrials.gov
Start date
2 January 2026
Est. completion
21 May 2029

Where this trial is recruiting

🇦🇺 Australia 🇰🇷 South Korea 🇬🇧 United Kingdom 🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov