Study of LMY-922 CAR-T Cells for Blood Cancers

This study is testing a new type of cell therapy called LMY-922 (BAFF CAR-T cells) for people with certain blood cancers that have come back or not responded to other treatments. These cancers include Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia, Hairy Cell Leukemia, and Multiple Myeloma. LMY-922 is designed to target specific proteins on cancer cells, even if previous treatments like CD19 CAR-T cells didn't work. The main goals are to see how safe LMY-922 is and to find the best dose. You may be able to join if you are 18-75 years old and have one of these blood cancers that has relapsed after at least two other treatments. The study plans to enroll 27 participants.

Study design
This is an interventional study, meaning participants will receive a specific treatment (LMY-922). It aims to enroll 27 participants to assess safety and determine the best dose.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The study will assess safety and dose for 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07679919

BAFF CAR-T Cells (LMY-922) for Treatment of Refractory Hematologic Malignancies

Not Yet Recruiting
PHASE1Ages 18–75InterventionalTreatment
Luminary Therapeutics
~27 participants
Updated 2026-07-01 on ClinicalTrials.gov
What's tested:LMY-922

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
To assess the safety profile of LMY-922 in patients with refractory hematologic malignancies.
Measured over 12 Months
+1 more outcome measured
Non-Hodgkin Lymphoma
Chronic Lymphocytic Leukemia
Hairy Cell Leukemia
Multiple Myeloma
1 sites across 1 states
Ohio1

Opens a ready-to-send draft in your own email app — review before sending.

  • To assess the safety profile of LMY-922 in patients with refractory hematologic malignancies.12 Months

    Incidence and severity of treatment-emergent adverse events

  • To determine the Recommended Phase II Dose of LMY-922 in patients with refractory hematologic malignancies.12 Months

    Incidence of dose limiting toxicities (DLT)