Active, not recruitingPhase 1NCT03330691
A Feasibility and Safety Study of Dual Specificity CD19 and CD22 CAR-T Cell Immunotherapy for CD19+CD22+ Leukemia
Studying Adult T-cell leukemia/lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Seattle Children's Hospital
- Principal Investigator
- Colleen Annesley, MDSeattle Children's Hospital
- Intervention
- Patient-derived CD19- and CD22 specific CAR(biological)
- Enrollment
- 78 target
- Eligibility
- 30 years · All sexes
- Timeline
- 2017 – 2035
Study locations (5)
- Children's Hospital Los Angeles, Los Angeles, California, United States
- Children's National Medical Center, Washington D.C., District of Columbia, United States
- Riley Hospital for Children, Indianapolis, Indiana, United States
- Seattle Children's Hospital, Seattle, Washington, United States
- Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT03330691 on ClinicalTrials.govOther trials for Adult T-cell leukemia/lymphoma
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