Myeloma Trial, Recruiting NCT05053607 Sponsor: Pack Health Condition: Myeloma
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Myeloma Trial, Recruiting

NCT05053607
Recruiting Not Applicable

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.

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Pack Health
Registry
ClinicalTrials.gov
Start date
17 June 2022
Est. completion
31 August 2025

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in Patient's Qualitative Assessment of Treatment Real World version (PQAT-RW); Qualitative Interview

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