Phase 3 Myeloma Trial, Recruiting NCT06296121 Sponsor: Biocad Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT06296121
Recruiting Phase 3

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 signed a consent form agreeing to take part in the study.
  • People aged 18 or older at the time of signing the consent form.
  • People with a confirmed diagnosis of multiple myeloma, diagnosed using standard international criteria.
  • People whose myeloma can be measured through blood or urine tests at the start of the study (specific protein or light chain levels must meet defined thresholds — confirm with trial site).
  • People whose myeloma showed at least a partial response to at least one previous treatment.
  • People whose myeloma has come back and stopped responding to treatment, and who have previously been treated with two specific types of myeloma therapy known as proteasome inhibitors and immunomodulatory drugs.
  • People with a general health and activity level rated as reasonably functional (scored 0–2 on a standard medical scale — confirm with trial site).
  • People who are not pregnant and who are willing to use contraception during the study.
  • People who agree to have a bone marrow biopsy as part of the study.

Who may not be able to join:

  • People who have previously been treated with daratumumab or any other therapy that targets a protein called CD38.
  • People who received myeloma treatment within 2 weeks (or within 5 half-lives of the drug) before joining the study, except for a short course of steroid medication.
  • People who had a stem cell transplant using their own cells within 12 weeks before joining the study.
  • People who have ever had a stem cell transplant using donor cells, regardless of when it occurred.
  • People who have a stem cell transplant planned before their disease progresses during this study.
  • People diagnosed with plasma cell leukemia, POEMS syndrome, or amyloidosis.
  • People with a condition called Waldenström macroglobulinemia or similar conditions involving high levels of a certain protein, where there is no evidence of the specific bone-affecting cell growth seen in multiple myeloma.
  • People who have had another cancer in the past 5 years, except for certain early-stage or non-invasive skin or cervical cancers that have been fully treated and are considered low risk for returning (confirm with trial site).
  • People who have undergone a plasma-filtering procedure called plasmapheresis within 28 days before joining the study.
  • People who show signs that their myeloma has spread to the membranes surrounding the brain or spinal cord.
  • People who are pregnant or breastfeeding, or who are planning a pregnancy during the study or within 3 months after the last dose of the study drug. This also applies to male participants who are planning to father a child during the study or within 3 months after the last dose.

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 20 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.

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Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Biocad
Registry
ClinicalTrials.gov
Start date
21 December 2023
Est. completion
1 January 2025

Where this trial is recruiting

🇷🇺 Russia

Primary endpoints

Overall response rate according to IMWG (International Myeloma Working Group) criteria

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: 20 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