LMY-920 for Treatment of Relapsed or Refractory Myeloma
Part of paid clinical trials in Cleveland, Ohio.
- Sponsor
- Luminary Therapeutics
- Study ID
- NCT05546723
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Multiple Myeloma in Relapse
- Multiple Myeloma, Refractory
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Autologous CAR-T cell therapy expressing the BAFF-ligand. — BIOLOGICALLMY-920
Study Details
Since CAR-T cell treatment of refractory myeloma has shown success, based on preclinical data, we posit that CAR-T cells expressing B-cell activating factor (BAFF) can become another strategy to treat refractory myeloma, even after relapse following BCMA targeting CAR-T cell treatment. This will be phase 1 study of BAFF ligand CAR-T cells in relapsed and refractory myeloma.
Key Dates
- Start date
- Mar 13, 2024
- Status verified
- Oct 2024
- Primary completion
- Jul 31, 2025
- Completion
- Oct 31, 2025
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: LMY-920 dose escalationOpen label, dose escalation study with up to four dose levels of LMY-920. The maximum tolerated dose (MTD) of LMY-920 will be determined using dose-escalation 3+3 design.
Primary Outcome Measure
To determine recommended phase II dose of human LMY-920 in patients with relapsed or refractory myeloma. [ Time Frame: 24 months ]
Central Contacts
- Leland Metheny, MD(216) 844-0139
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University Hospitals Seidman Cancer Center | Cleveland | Ohio | 44106 |
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