Skip to content

Study for sequential chimeric antigen receptor T cells targeting at different B-cell antigens in relapsed B-cell acute lymphoblastic leukemia after allogeneic hematopoietic stem cell transplantation

Study for sequential chimeric antigen receptor T cells targeting at different B-cell antigens in relapsed B-cell acute lymphoblastic leukemia after allogeneic hematopoietic stem cell transplantation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022209
Enrollment
Unknown
Registered
2019-03-30
Start date
2019-03-27
Completion date
Unknown
Last updated
2019-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed B acute lymphoblastic leukemia after allo-HCT

Interventions

Sponsors

Beijing Boren Hospita
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Relapsed or refractory patients who have been diagnosed as CD19+/CD22+/CD20+ B-cell acute lymphoblastic leukemia (> 99% of leukemia cells express CD19/CD22/CD20),and all of these patients relapsed after allogeneic hematopoietic stem cell transplantation(In line with NCCN,2015.2); 2. Aged 1 to 70 years; 3. Patients with self-awareness and older than 18 years, who have the ability to sign the consent form and voluntary consent; 4. Pediatric patients' legal guardians or the clients authorized by patients sign the consent form and are voluntary to participate in the clinical trials.

Exclusion criteria

Exclusion criteria: 1. Intracranial hypertension or unconsciousness; 2. Symptomatic heart failure or severe cardiac arrhythmia; 3. Respiratory failure; 4. With other types of malignant tumors; 5. Disseminated intravascular coagulation; 6. Serum creatinine and/or urea nitrogen=1.5 ×normal; 7. Sepsis or other uncontrolled active infection; 8. Uncontrolled diabetes; 9. Severe mental disorder; 10. Obvious intracranial lesions examined by head MRI; 11. Cerebrospinal fluid leukemia cells> 20/ul; 12. Ratio of blood leukemia cell > 30%; 13. WHO physical status classification level=3; 14. Organ transplant recipients; 15. Pregnant or lactating women; 16. With =3 aGVHD or activity and widely cGVHD.

Design outcomes

Primary

MeasureTime frame
safety;Ratio of bone marrow and peripheral B leukemia cells;

Countries

China

Contacts

Public ContactChunrong Tong

Beijing Boren Hospital

dongq@borenhospital.com+86 15210562236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026