Phase 2 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 whose physical functioning and activity level meets a specific standard, rated 0 or 1 on a medical scale used to measure how well a person can carry out daily activities (confirm with trial site)
- People with multiple myeloma who have already received at least 3 different treatment regimens, including at least one treatment from each of three specific drug types: anti-CD38 antibodies, immunomodulatory drugs (IMiDs), and proteasome inhibitors — and whose disease has continued to grow or spread after their most recent treatment
- People whose disease is measurable in a way that allows doctors to track treatment response (confirm with trial site)
- People whose blood counts, liver, and kidney are functioning at an adequate level as defined by the trial (confirm with trial site)
Who may not be able to join:
- People diagnosed with plasma cell leukemia, primary systemic light-chain amyloidosis, Waldenström macroglobulinemia, or POEMS syndrome
- People who have received any cancer treatment within either 28 days before the first study drug dose, or within 5 half-lives of their previous treatment — whichever period is shorter
- People who have had a donor stem cell transplant within the past 6 months, or their own stem cell transplant within the past 12 weeks
- People who have taken steroid medications above a certain dose within 72 hours before the start of the study drug (confirm with trial site)
- People with known involvement of multiple myeloma in the brain or nervous system, a suspected or known condition called progressive multifocal leukoencephalopathy, a history of a brain or nervous system disorder, or a seizure within the past 12 months
- People who have received a live or live-attenuated vaccine within 28 days before the first study drug dose
- People who have received a COVID-19 vaccine within 1 week before the planned start of the study medication
- People who have had a blood disorder called myelodysplastic syndrome, or another cancer in the past 3 years — with some exceptions such as certain skin cancers, early-stage thyroid cancer, low-risk early prostate cancer, or carcinoma in situ (confirm with trial site)
- People with significant heart or cardiovascular disease as defined by the trial (confirm with trial site)
- People with uncontrolled HIV, Hepatitis B, Hepatitis C, or other uncontrolled infections such as CMV
- People with a known allergy to both allopurinol and rasburicase (two medications used to manage certain side effects)
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
6 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Incidence of dose limiting toxicities (DLTs) from the first dose of REGN7945 in combination with linvoseltamab; Incidence of treatment emergent adverse events (TEAEs) during the treatment period with REGN7945 in combination with linvoseltamab; Severity of TEAEs during the treatment period with REGN7945 in combination with linvoseltamab; Very Good Partial Response (VGPR) or better as determined by the investigator using the International Myeloma Working Group (IMWG) response criteria in patients receiving combination therapy; VGPR or better as determined by the investigator using the IMWG respo...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.