Phase I Trial of Universal Donor NK Cell Therapy in Combination With ALT803
NCT02890758 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2023-02-21
Summary
The purpose of this study is to find the number of natural killer (NK) cells from non-HLA matched donors that can be safely infused into patients with cancer. NK cells are a form of lymphocytes that defend against cancer cells. NK cells in cancer patients do not work well to fight cancer. In this study, the NK cells are being donated by healthy individuals without cancer who are not "matched" by human leukocyte antigen (HLA) genes to patients. After receiving these NK cells, patients may also be given a drug called ALT803. ALT803 is a protein that keeps NK cells alive, helps them grow in number and supports their cancer-fighting characteristics. HLA-unmatched NK cell infusion is investigational (experimental) because the process has not approved by the Food and Drug Administration (FDA).
Conditions
- Acute Myeloid Leukemia
- Myelodysplastic Syndrome
- Acute Lymphoblastic Leukemia
- Chronic Myeloid Leukemia
- Chronic Lymphocytic Leukemia
- Non Hodgkin Lymphoma
- Hodgkin Lymphoma
- Myeloproliferative Syndromes
- Plasma Cell Myeloma
- Colon Carcinoma
- Adenocarcinoma of Rectum
- Soft Tissue Sarcoma
- Ewing's Sarcoma
- Rhabdomyosarcoma
Interventions
- BIOLOGICAL
-
Natural Killer (NK) Cells
Dose escalation of Natural Killer (NK) Cells from two infusion of starting at Dose Level 1 (1x10\^7 cells/kg), dose Level-1 (1x10\^6 cells/kg) if 2 of 6 patients at Level 1 develop DLTs. Escalation to dose level 2 (2.5X10\^7) and Dose level 3 (5X10\^7) is dependent on DLT
- BIOLOGICAL
-
ALT803
given at 6mcg/kg weekly for four weeks
Sponsors & Collaborators
-
Brenda Cooper, MD
lead OTHER
Principal Investigators
-
David Wald, MD, PhD · University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-05-22
- Primary Completion
- 2021-06-01
- Completion
- 2023-02-17
- FDA Drug
- Yes
Countries
- United States
Study Locations
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