UKM Medical Centre
Bandar Tun Razak, Kuala Lumpur, 56000, Malaysia
Location status: Recruiting
Location contact
S Fadilah Abdul Wahid, MD, DrIntMed, PhD
CONTACT
Wan Fariza Wan Jamaludin, MD,DrIntMed
CONTACT
NCT Number: NCT03937544
This is Phase II / III, Prospective, single arm, Open Label Study to Evaluate Safety and Efficacy of Intravenous Autologous CD19 CAR-T Cells for Relapsed / Refractory B-Acute Lymphoblastic Leukaemia
Interested in participating?
Request Info13 year–65 year
All sexes
Interventional
Phase 2 / Phase 3
Bandar Tun Razak, Kuala Lumpur, 56000, Malaysia
Location status: Recruiting
S Fadilah Abdul Wahid, MD, DrIntMed, PhD
CONTACT
Wan Fariza Wan Jamaludin, MD,DrIntMed
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CD19 CAR-T cells will be administered after completion of the lymphodepletion chemotherapy.
Patients will receive lymphodepleting chemotherapy consisting of Cyclophosphamide 250 - 300 mg/m2/day IV(Day -5, Day -4, Day -3 ).
Patients will receive lymphodepleting chemotherapy consisting of Fludarabine 25-30 mg/m2/day IV (Day -5, Day -4, Day -3 ).
Time frame: Participants will be followed for the duration of the treatment, with an expected average of 3 months.
Overall Response Rate (ORR) defined as Complete Response (CR) and CR with incomplete blood recovery (CRi) according to WHO criteria.
Time frame: 12 Months
Duration of response defined from the time when criteria for response (CR or CRi) are met to the first documentation of relapse or progression.
Time frame: 12 Months
Duration of response defined from the time when criteria for response (CR or CRi) are met to the first documentation of relapse or progression.
Time frame: 12 Months, 24 Months
Overall Survival (OS) defined as the time from treatment to the date of death due to any cause.
Time frame: 12 Months, 24 Months
Progression Free Survival (PFS) defined as the time from treatment to first documentation of objective leukemic progression (date of leukaemia assessment documenting progressive disease) or to death due to any cause. Progression is assessed by BM biopsy or CSF analysis according to NCCN criteria. It is assessed at Day 30 and monthly thereafter, or earlier if clinically indicated.
Time frame: 12 Months, 24 Months
Time To Next Treatment (TTNT) defined as the end of study treatment until the institution of the next therapy.
Time frame: 30 days
Percentage of participants with adverse events
Contact information is provided by the study sponsor or research team.
National University of Malaysia
Other
A Phase II/III Prospective, Open Label Study to Evaluate Safety and Efficacy of Intravenous Autologous CD19 CAR-T Cells for Relapsed/ Refractory B-Acute Lymphoblastic Leukaemia
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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