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 are able and willing to give their consent to participate, or who have a legally authorised representative who can give consent on their behalf.
- People who have been diagnosed with multiple myeloma (MM) that requires whole-body (systemic) treatment, according to recognised international guidelines.
- People who have recently started a treatment called HyQvia — either no more than 30 days before joining the study or having received no more than 2 doses — or people who are expected to start HyQvia within 30 days after the enrolment visit.
- People who were 18 years of age or older at the time their multiple myeloma was diagnosed.
- People who have available medical records going back to when their multiple myeloma was first diagnosed and treatment was needed.
- People whose doctor estimates they have a life expectancy of more than 6 months at the time of joining the study.
- People whose general health and ability to carry out daily activities falls within a certain range, as measured by a standard medical scoring tool (confirm with trial site).
- People who are willing and able to follow all the requirements set out in the study plan.
Who may not be able to join:
- People who are known to have an allergic reaction or sensitivity to any ingredient in HyQvia.
- People who have a primary immune deficiency condition, or who have been diagnosed with HIV/AIDS, active hepatitis C, or active hepatitis B.
- People who have used immunoglobulin (Ig) therapy or prevention treatment within the 3 months before joining the study.
- People who have a serious infection that requires intravenous (drip) antibiotics at the time of joining — though people taking a short course of antibiotic tablets may still be eligible (confirm with trial site).
- People who have taken part in another clinical trial involving a medicine or medical device within the 30 days before joining, or who plan to do so during this study. Note: people receiving investigational CAR-T cell therapies or bispecific antibody treatments may still be eligible (confirm with trial site).
- People who have a stem cell transplant planned during the study period, or who have previously had a certain type of stem cell transplant — specifically, a transplant using donor cells at any point in the past, or a transplant using their own cells within 3 months before joining.
- People who have had another cancer (other than multiple myeloma) within the 3 years before joining — with some exceptions for certain early-stage or low-risk skin, cervical, breast, or prostate conditions (confirm with trial site).
- People who have had major surgery within 2 weeks before joining, who have not fully recovered from a previous surgery, or who have major surgery planned during the study period. Note: minor procedures under local anaesthetic, and certain spinal procedures, are not considered major surgery (confirm with trial site).
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: Study Director, Takeda
Phone: +1-877-825-3327
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
Dose of HyQvia per Kilogram of Body Weight; Absolute Dose of HyQvia per Infusion; Treatment Interval; Infusion Volume per Site; Total Infusion Volume; Infusion Rate; Duration of Infusion; Location of Infusion Sites; Number of Infusion Sites; Number of Participants Characterized by Site of Care; Length and Diameter of Infusion Needles; Number of Participants per Type of Pump; Number of Participants With Availability of Caregiver Support; Number of Training Visits; Number of Participants With Infusions That are Discontinued, Slowed, or Interrupted; Number of Participants With Reasons of infusion...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.