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 aged 18 or older
- People who have been diagnosed with multiple myeloma that has come back or stopped responding to previous treatment, in a way that matches the FDA's official guidelines for the drug isatuximab-irfc (Sarclisa®)
- People whose treating doctor has confirmed or is planning treatment with isatuximab-irfc given through an IV (directly into a vein) as part of their standard cancer care — taking other medications at the same time, such as pomalidomide, is permitted
- People who have access to a smartphone or similar device that can send and receive text messages, emails, or run a mobile app, and who are willing to use it as part of the trial
- People who are willing to wear a Fitbit device and have health data collected from it
- People who are physically able to do some level of physical activity, as measured by a standard medical scale called the ECOG performance status score of 2 or lower (confirm with trial site what this means for a specific situation)
Who may not be able to join:
- People who are terminally ill, meaning their doctor has indicated they are likely to have 6 months or less to live, or those who have moved to comfort-focused care only (supportive care without treatment aimed at the illness itself)
- People whose medical records show they are not able to give their own informed consent to participate
- People who are receiving isatuximab-irfc by injection under the skin (subcutaneously) rather than through an IV
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: Melody R Becnel, MD, M.D. Anderson Cancer Center
Phone: 205-721-7542
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
Change in Patient's Qualitative Assessment of Treatment Real World version (PQAT-RW); Qualitative Interview
Can't join this trial?
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.