Phase 2 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:
- Adults aged 18 or older, of any gender.
- People who have been formally diagnosed with multiple myeloma based on established international diagnostic guidelines.
- People who have already been through at least 3 separate courses of treatment for multiple myeloma, or whose myeloma has stopped responding to two specific types of standard treatments (an IMiD and a PI, as defined by international guidelines).
- People who still have measurable signs of the disease at the time of screening, according to international myeloma guidelines.
- People whose general physical functioning falls within a certain range on a standard medical scale (rated 0 to 2 out of 4, meaning independent or only mildly limited in daily activities).
- People whose heart, lungs, liver, kidneys, and blood counts meet certain minimum health thresholds set out in the trial protocol (confirm with trial site for specific values).
- Women who could become pregnant must have a negative pregnancy test and agree to use effective contraception throughout the trial.
- People who have read and understood the trial's consent form and are willing to sign it — those who cannot sign due to being unable to read may do so with an impartial witness present.
- People who are willing and able to follow all of the trial's procedures, schedules, and requirements throughout the study.
Who may not be able to join:
- People who have previously received any CAR-T cell therapy, or any treatment specifically targeting a protein called BCMA.
- People who have a current or past history of multiple myeloma affecting the brain or spinal cord, or who show signs of this.
- People who have had a stroke or seizure within the 6 months before signing the consent form.
- People with an active, uncontrolled infection, including uncontrolled bacterial, fungal, hepatitis B, hepatitis C, or HIV infection.
- People with significant heart disease or severe lung disease (confirm with trial site for specific definitions).
- People who have recently received a bone marrow transplant from a donor and are still experiencing transplant-related immune complications or are on immune-suppressing medication for this reason.
- People who are pregnant, breastfeeding, or planning to become pregnant during the trial or within one year of receiving the study treatment.
- People with any other condition that, in the treating doctor's judgement, would make participation unsafe, unsuitable, or interfere with the trial's assessments.
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: Maryam Khan, MBBS, MRCP (UK), FCPS(Cl Haem), National University of Medical Sciences
Phone: +923315582265
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
Assess Safety /tolerability and feasibility of manufacturing and delivering the product
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.