A Study of Obecabtagene Autoleucel in People With B-cell Acute Lymphoblastic Leukemia
Part of paid clinical trials in Stanford, California.
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Study ID
- NCT07400029
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Obecabtagene Autoleucel — DRUGGiven as infusion. Obe-cel dose 1: Obe-cel will be administered 3 days (+/- 1 day) after completion of lymphodepleting chemotherapy, allowing a minimum of 48 hour washout from the last dose of lymphodepleting chemotherapy.
Study Details
The researchers are doing this study to find out whether obecabtagene autoleucel (obe-cel) is an effective treatment for people with B-cell acute lymphoblastic leukemia (ALL) that is in complete remission (CR, meaning all signs of cancer are gone) with no measurable residual disease (MRD-negative, meaning there are no detectable cancer cells). Participants in this study will have received past treatment for their B-cell ALL, and their disease will be in MRD-negative CR for the first time (first MRD-negative CR).
Key Dates
- First listed
- Feb 10, 2026
- Start date
- Feb 3, 2026
- Status verified
- Jun 2026
- Primary completion
- Feb 28, 2029
- Completion
- Feb 28, 2029
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort Awill enroll Philadelphia chromosome negative patients
- Experimental: Cohort Bis an exploratory cohort that will enroll Philadelphia chromosome positive patients
Primary Outcome Measure
relapse free survival (RFS) (Cohort A) [ Time Frame: 1 year from infusion ]
Central Contacts
- Ioannis Kalogirou Valtis, MD646-608-2091
- Mark Geyer, MD646-608-3745
Locations (8)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford University (Data Collection AND Specimen Analysis) | Stanford | California | 94305 | Lori Muffly, MD 650-498-6000 |
| Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) | Basking Ridge | New Jersey | 07920 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Monmouth (Limited Protocol Activities) | Middletown | New Jersey | 07748 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Bergen (Limited Protocol Activities) | Montvale | New Jersey | 07645 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Cancer Commack - Suffolk (Limited Protocol Activities) | Commack | New York | 11725 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Westchester (Limited Protocol Activities) | Harrison | New York | 10604 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Cancer Center (All Protocol Activities) | New York | New York | 10065 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
| Memorial Sloan Kettering Nassau (Limited Protocol Activities) | Uniondale | New York | 11553 | Ioannis Kalogirou Valtis, MD 646-608-2091 |
Find similar trials in Stanford, CA
By condition
By specialty
By research site
Stanford University (Data Collection AND Specimen Analysis)· Stanford, CAMemorial Sloan Kettering at Basking Ridge (Limited Protocol Activities)· Basking Ridge, NJMemorial Sloan Kettering Monmouth (Limited Protocol Activities)· Middletown, NJMemorial Sloan Kettering Bergen (Limited Protocol Activities)· Montvale, NJMemorial Sloan Kettering Cancer Commack - Suffolk (Limited Protocol Activities)· Commack, NYMemorial Sloan Kettering Westchester (Limited Protocol Activities)· Harrison, NY
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