Phase 2 Myeloma Trial, Recruiting NCT06669247 Sponsor: Regeneron Pharmaceuticals Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06669247
Recruiting Phase 2 🇦🇺 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 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.

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 8 July 2026
Phase 2: approximately ~30% 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

Royal Prince Alfred Hospital, Sydney, New South Wales
Illawarra Cancer Care Centre, Wollongong, New South Wales
Pindara Private Hospital, Benowa, Queensland
Royal Adelaide Hospital, Adelaide, South Australia
Alfred Hospital, Melbourne, Victoria
St Vincents Hospital Melbourne, 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 2
Sponsor
Regeneron Pharmaceuticals
Registry
ClinicalTrials.gov
Start date
11 December 2024
Est. completion
11 November 2033

Where this trial is recruiting

🇦🇺 Australia 🇬🇧 United Kingdom

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?

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: 8 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