Phase 2 Myeloma Trial, Recruiting NCT06292780 Sponsor: Regeneron Pharmaceuticals Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06292780
Recruiting Phase 2

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.

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 28 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

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
7 August 2024
Est. completion
20 August 2028

Where this trial is recruiting

🇬🇷 Greece 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

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?

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: 28 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