About this trial
A Clinical Study to Investigate the Safety, Efficacy, and Cellular Metabolism of CT1190B CAR-T Cell therapy, in Patients with Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants must voluntarily sign the informed consent form (ICF) and must be willing and be able to adhere to the study visit schedule and other protocol requirements and agree to be in long term follow-up (LTFU) for up to 15 years as mandated by the regulatory guidelines.
18-75 years old;
Histologically or cytologically confirmed B-NHL;
Previously received at least 2 lines of systemic therapy;
Disqualifiers
Pregnant or lactating women;
Has HIV, syphilis infection, active hepatitis B virus infection (HBsAg positive and HBV-DNA above the detection limit), or active hepatitis C virus infection (HCV antibody and HCV-DNA positive);
Has any current uncontrolled active infection, including but not limited to participants with active tuberculosis (investigator 's judgment);
Participants' toxicities caused by previous treatment did not recover to Common Terminology Criteria for Adverse Events (CTCAE) ≤ Grade 1, except alopecia and other events that are judged tolerable by the investigator;
Trial design
Single group
Treatments tested in this trial
CAR T cells
Drugchimeric antigen receptor T cells
Treatment groups
Trial outcomes
Primary outcomes
Adverse Events (AE) after CT1190B infusion
An assessment of severity grade will be made according to the National Cancer Institute Common Terminology Criteria
MTD and/or dose range
Evaluate Dose limited toxicity and recommended dosage range after CT0991 infusion.
Secondary outcomes
Overall response rate(ORR)
The proportion of patients with complete remission (CR) /partial response (PR) after CT1190B infusion.
Complete response rate (CRR)
The proportion of patients with complete response(CR) after CT1190B infusion
Duration of remission(DOR)
Participants achieving CR/PR will be included in the analysis set for DOR. DOR is defined as the time from the date of confirmed response until the date of disease relapse or death from any cause, whichever occurs first.
Time to response (TTR)
The time from cell infusion to the first assessment of CR or PR
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Kai Hu
Lead sponsor
Beijing GoBroad Hospital
Sponsor institution