This study is a first-in-human, single-arm, open-label Phase I/II study of nula-cel in approximately 15 participants, diagnosed with severe Sickle Cell Disease. The primary objective is to evaluate safety of the treatment in this patient population, as well as preliminary efficacy and pharmacodynamic data.
Participants diagnosed with severe SCD will receive nula-cel via IV infusion following myeloablative conditioning in an autologous HSCT setting.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
nula-cel is administered via IV infusion following a myeloablative conditioning regimen
Children's Hospital Los Angeles
Los Angeles, California, United States
RECRUITINGLucile Packard Children's Hospital
Palo Alto, California, United States
RECRUITINGWashington University
St Louis, Missouri, United States
Proportion of patients who reach neutrophil engraftment
Time frame: 42 days post-infusion
Incidence rate of treatment-related mortality
Time frame: 100 days post-infusion
Incidence rate of treatment-related mortality
Time frame: 12 months post-infusion
Overall survival
Time frame: 24 months post-infusion
Frequency and severity of AEs/SAEs
Time frame: 24 months post-infusion
Time to neutrophil engraftment
Time frame: through study completion, up to 24 months post-infusion
Time to platelet engraftment
Time frame: through study completion, up to 24 months post-infusion
Evaluation of gene correction levels in peripheral myeloid cells
Time frame: through study completion, up to 24 months post-infusion
Evaluation of adult Hgb as a percentage of total Hgb
Time frame: through study completion, up to 24 months post-infusion
Evaluation of HbS as a percentage of total Hgb
Time frame: through study completion, up to 24 months post-infusion
Total Hgb without disease-indicated transfusion support
Time frame: through study completion, up to 24 months post-infusion
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Columbia University Irving Medical Center
New York, New York, United States
RECRUITINGMemorial Sloan Kettering
New York, New York, United States
RECRUITINGNationwide Children's Hospital
Columbus, Ohio, United States
RECRUITINGChange in annualized packed red blood cell (pRBC) transfusion requirements (volume and frequency) for SCD indications
Time frame: through study completion, up to 24 months post-infusion
Proportion of participants with complete resolution of severe vaso-occlusive crises (sVOCs)
Time frame: over time, from 6 months to 18 months post-infusion
Incidence rate of any sVOCs
Time frame: over time, from 6 months to study completion, up to 24 months post-infusion
Proportion of participants achieving HbS <50% for at least 3 months
Time frame: through study completion, up to 24 months post-infusion
Evaluation of globin chain expression compared to baseline
Time frame: through study completion, up to 24 months post-infusion