Phase 3 Myeloma Trial, Recruiting NCT07582432 Sponsor: Grifols Biologicals, LLC Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT07582432
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 have been diagnosed with B-cell chronic lymphocytic leukemia (a type of blood cancer) at an intermediate or high stage, based on specific medical criteria
  • You have been diagnosed with multiple myeloma (a bone marrow cancer) at stage II or III, based on specific medical criteria
  • You have been diagnosed with a B-cell non-Hodgkin lymphoma (another type of blood/lymph node cancer) at stage III or higher, including cases that have come back or stopped responding to treatment
  • You have low levels of a key immune protein called IgG (below 5g/L) as measured at your screening appointment

Who may not be able to join:

  • You received a stem cell transplant from a donor within the last 6 months
  • You are currently receiving, or have received in the last 6 months, antibody/immunoglobulin replacement therapy (a treatment that boosts your immune proteins)
  • You currently have an active infection of any kind
  • You have another active cancer in addition to the one being studied
  • You have a condition called primary immunodeficiency (a specific inherited immune system disorder)
  • Your doctors estimate you have less than 1.5 years to live
  • You have another serious ongoing illness that the trial doctor believes could interfere with the study or put you at extra risk
  • You have previously had a serious allergic reaction to immunoglobulin treatments, blood, or any blood-based products
  • You have a specific condition called Selective IgA Deficiency (confirm with trial site)
  • You are pregnant, breastfeeding, have tested positive for pregnancy at screening, or are unwilling to use a reliable form of contraception throughout the study (a list of acceptable methods is defined by the trial)
  • You have severe kidney disease, specifically a kidney function score below a certain level as measured by a blood test (confirm with trial site)
  • Your liver enzyme levels (measured by a blood test at screening) are more than three times higher than the normal range
  • You have a history of blood clots or related events — such as deep vein thrombosis, pulmonary embolism, stroke, heart attack, or certain other circulation problems — either once in the past year or twice in your lifetime
  • You currently have a condition that causes your blood to be too thick or to clot too easily
  • You currently have signs or symptoms of an active hepatitis B or hepatitis C infection
  • You have uncontrolled high blood pressure (above specific levels) or a resting heart rate above 100 beats per minute
  • You have had a known problem with substance or prescription drug misuse in the past 12 months
  • You have taken part in another interventional clinical trial (one involving an experimental treatment unrelated to your current cancer) within the last 30 days
  • You or your caregiver are unwilling or unlikely to follow the study rules and procedures throughout the trial

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 13 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

Phone: +49 6103 801-6395,

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
Sponsor
Grifols Biologicals, LLC
Registry
ClinicalTrials.gov
Start date
23 April 2026
Est. completion
31 August 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

serious bacterial infection (SBI) rate per-participant per year.

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: 13 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