Skip to content

Clinical study of autologous mouse-derived BCMA-CART in the treatment of relapsed and refractory multiple myeloma

Clinical study of autologous mouse-derived BCMA-CART in the treatment of relapsed and refractory multiple myeloma

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024388
Enrollment
Unknown
Registered
2019-07-09
Start date
2019-07-03
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

Relapsed and refractory multiple myeloma

Interventions

treatment group:Murine BCMA-CART Cell Immunotherapy

Sponsors

Beijing Boren Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with relapsed or refractory multiple myeloma with CART treatment target (BCMA or CD269); 2. Patients must have evaluable disease certificates, including minimal residual disease; 3, Aged 18 to 70 years, including the boundary value, have the ability to know, can sign informed and voluntary consent; 4. The estimated survival period is more than 3 months; 5, ECOG score 0-2 points; 6. Women of childbearing age were negative for the blood pregnancy test before the start of the trial and agreed to take effective contraceptive measures during the trial period until the last follow-up.

Exclusion criteria

Exclusion criteria: 1. Intracranial hypertension or unconsciousness; 2. Symptomatic heart failure or severe arrhythmia; 3. Respiratory failure; 4. With other types of malignant tumors; 5. Diffuse vascular internal coagulation; 6. Serum creatinine and / or urea nitrogen >= 1.5 times the normal value; 7. Sepsis or other uncontrollable infections; 8. Uncontrollable diabetes; 9. Severe mental disorders; 10. Head MRI examination has obvious lesions in the skull; 11. Examination of leukemia cells by cerebrospinal fluid > 20/ul; 12. The proportion of blood tumor cells is >30%; 13. Organ transplant recipients.

Design outcomes

Primary

MeasureTime frame
safety;complete remission rate;Progression-free survival (PFS);

Countries

China

Contacts

Public ContactChunrong Tong, Xiaoyan Ke

Beijing Boren Hospital

dongq@borenhospital.com+86 15210562236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026