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 who have been diagnosed with a specific type of amyloidosis called AL amyloidosis, confirmed according to the trial's guidelines
- People whose disease can be measured through a specific blood test that looks at proteins called free light chains
- People who have already received at least one previous treatment for their condition and whose doctor believes they need further treatment
- People whose level of a heart-related protein in the blood (NT-proBNP) is at or below a certain level during the screening period
- People whose liver, blood, kidneys, and heart are all functioning adequately, as defined by the trial's guidelines
- People who are reasonably able to carry out daily activities, based on a standard medical scoring system (a score of 2 or lower on the ECOG scale)
Who may not be able to join:
- People who have a history of a different type of amyloidosis (other than AL amyloidosis)
- People whose bone marrow biopsy or sample shows more than 60% of a certain type of abnormal cell (plasma cells) during screening
- People found to have certain bone damage or tumours outside the bone marrow on imaging scans during screening
- People who have had a heart attack within the six months before their first screening visit
- People who have had an active infection requiring hospital care or treatment with intravenous (IV) antibiotics or antifungals within 28 days before starting the study drug
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
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
Primary endpoints
Incidence of dose-limiting toxicity (DLTs); Achievement of hematologic complete response (CR) as determined by the Independent Review Committee (IRC)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.