Phase 3 Myeloma Trial, Recruiting NCT06561854 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT06561854
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:

  • You are 18 years old or older
  • You have been diagnosed with multiple myeloma (MM) that has come back after previous treatment
  • You have received between 1 and 3 previous treatment plans for multiple myeloma (where each plan included at least 2 cycles of treatment)
  • You are eligible to receive one of two specific drug combinations: either isatuximab + pomalidomide + dexamethasone, or isatuximab + carfilzomib + dexamethasone
  • Your previous treatment worked at least partially (meaning your myeloma responded to it)
  • You are reasonably active and able to care for yourself, with only mild limitations on daily activities (confirm with trial site)
  • Any side effects from your previous treatments have either gone away or have stabilised
  • You are willing and able to sign a consent form agreeing to take part

Who may not be able to join:

  • You have a known allergy or medical reason why you cannot take the study medicines
  • Your myeloma has stopped responding to, or you could not tolerate, a type of drug called an anti-CD38 antibody
  • You have previously been treated with the specific drug combinations used in this trial (pomalidomide-based or carfilzomib-based combinations as described above)
  • You have previously had a donor stem cell transplant (from another person)
  • You are planning to have a stem cell transplant before your disease gets worse
  • You have been diagnosed with another cancer in the past 3 years (some exceptions may apply, such as certain minor skin cancers — confirm with trial site)
  • Your multiple myeloma has spread to the fluid around the brain or spinal cord
  • You have a related but different blood condition, such as plasma cell leukaemia, Waldenström's macroglobulinemia, POEMS syndrome, or amyloidosis
  • You have another serious medical condition or active infection that could interfere with the trial
  • You have uncontrolled chronic lung disease (COPD)
  • You have a significant heart condition
  • You have an active hepatitis B infection confirmed by a specific blood test
  • You are HIV positive or have hepatitis C
  • You are currently breastfeeding
  • You are already taking part in another clinical trial involving a treatment
  • You are unable to give written consent to take part

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 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.

Contact this trial

Principal Investigator: Mohamad MOHTY, PU-PH, Assistance Publique - Hôpitaux de Paris

Phone: + 33 1 49 28 26 20

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 3
Registry
ClinicalTrials.gov
Start date
12 December 2024
Est. completion
1 December 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

overall response rate (ORR).

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