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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04601181
Other study ID # ThisCART22
Secondary ID
Status Recruiting
Phase Phase 1
First received
Last updated
Start date October 23, 2020
Est. completion date October 15, 2023

Study information

Verified date October 2020
Source Fundamenta Therapeutics, Ltd.
Contact Xingbing Wang, M.D.
Phone +8613856007984
Email wangxingbing@ustc.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a single-center, nonrandomized, open-label, study to evaluate the safety and clinical activity of allogeneic CAR-T targeting CD22 in patients with refractory or relapsed CD22-positive B cell malignancies


Description:

The patients will receive infusion of ThisCART22 cells from health donor ,to evaluate the safety and efficacy of ThisCART22 Cells in patients with refractory or relapsed CD22-positive B cell malignancies. In this study, the dose range is 0.2-60 x10^6 cells per kg body weight (no more than 3.0 x 10^9 in total).


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 15, 2023
Est. primary completion date October 15, 2022
Accepts healthy volunteers No
Gender All
Age group 3 Years to 70 Years
Eligibility Inclusion Criteria: 1. Subjects who volunteered to participate in the research and signed a written informed consent; 2. The informed consent was signed between the ages of 3-70, regardless of gender or race; 3. CD22 positive hematologic malignancies with no alternative treatment options deemed by investigator. including those who are not eligible for allogeneic stem cell transplantation (SCT) due to the following reasons: 3.1 age; 3.2 Concurrent disease; 3.3 Other contraindications, such as contraindications to total body irradiation (TBI) (TBI is one of the important treatment measures before allogeneic stem cell transplantation of ALL); 3.4 Lack of suitable donors; 3.5 Patients with relapse after CD19-CAR T treatment; 4. Estimated life expectancy > 12 weeks deemed by investigator 5. Recurrence after any stem cell transplantation (regardless of previous treatment regimen); 6. Patients who relapse after previous allogeneic SCT (myeloablative or non-myeloablative) and meet all the following entry criteria: 6.1 No active GVHD and no immunosuppression is required; 6.2 Transplant for more than 4 months; 7. Serum creatinine =1.6 mg/dl and/or BUN = 1.5 mg/dl; 8. Serum ALT/ AST < 5 upper limit of normal (ULN); 9. Measurable or detectable disease at time of enrollment,include minimal residual disease (MRD) detected by immunotyping, cytogenetics or PCR. 10. Cardiac ejection fraction = 40%. 11. Eastern cooperative oncology group (ECOG) performance status of = 2. 12. Female subjects with fertility have a negative pregnancy test result within 48 hours before the infusion and are not breast-feeding; all subjects with fertility potential before being enrolled in the study and throughout the study period until the last infusion Within 3 months, take adequate contraceptive measures. Exclusion Criteria: 1. Pregnant or lactating women; 2. Participated in another clinical trial during the first 4 weeks of the enrolled study or intended to participate in another clinical trial throughout the study period; 3. Have been treated with any gene product; 4. Uncontrolled infection; 5. History of HIV infection; 6. Active hepatitis B virus or hepatitis C virus infection; 7. Systemic steroid therapy may be required for cell infusion or collection, or there may be conditions that the investigator considers may require steroid therapy during blood collection or infusion.Corticosteroids for disease treatment are permitted, and inhaled steroids or hydrocortisone physiologic replacement therapy for patients with adrenocortical dysfunction is permitted beyond the time of cell collection or infusion; 8. Patients with grade 2-4 GVHD, or deemed need to manage by investigator; 9. The presence of GVHD under treatment;. 10. Patients with active CNS involvement by malignancy; 11. Patients combine with other disease cause neutrophil count (ANC) <750/uL or PLT< 50,000/uL 12. The researchers considered the subjects unsuitable for this clinical trial for various reasons.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
ThisCART22 cells injection
Assigned Interventions Biological/Vaccine: ThisCART22 cells 0.2-60 x 10^6 CAR-T cells per kg body weight. Intervention study

Locations

Country Name City State
China The First Affiliated Hospital of USTC (Anhui Provincial Hospital) Hefei Anhui

Sponsors (2)

Lead Sponsor Collaborator
Fundamenta Therapeutics, Ltd. The First Affiliated Hospital of USTC (Anhui Provincial Hospital)

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of AE or SAE of CART cell infusion in relation to the study drug at grade =3 (refer to CTCAE version 4.03); From infusion to week 12
Primary ORR (sum of CR and CRi) after infusion. From infusion to week 12
Secondary The survival time of CAR-T-22 cells in vivo; From infusion to month 12
Secondary ORR at week 4, 8, and 24 after infusion (ORR4, ORR8, ORR24). At week 4, 8, and 24 after infusion
See also
  Status Clinical Trial Phase
Recruiting NCT04384393 - Safety and Efficacy of ThisCART19 in Patients With Refractory or Relapsed B Cell Malignancies Phase 1
Completed NCT03953599 - CD19-Synthetic T Cell Antigen Receptor(STAR)-T in B-cell Malignancies Patients Phase 1