A Clinical Study Exploring CT1190B in the Treatment of Patients With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-75
SponsorKai Hu

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • CAR T cells

    Drug

    chimeric antigen receptor T cells

Treatment groups

24 Participants
are divided into 1 treatment group
Group A: CAR-T cells( chimeric antigen receptor T cells)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Adverse Events (AE) after CT1190B infusion

An assessment of severity grade will be made according to the National Cancer Institute Common Terminology Criteria

Time frame
12 months after CT1190B infusion
2

MTD and/or dose range

Evaluate Dose limited toxicity and recommended dosage range after CT0991 infusion.

Time frame
Up to 28 days after CAR-T cells infusion

Secondary outcomes

1

Overall response rate(ORR)

The proportion of patients with complete remission (CR) /partial response (PR) after CT1190B infusion.

Time frame
Evaluate at 4, 8, 12 weeks and 6,9,12month after CAR-T infusion
2

Complete response rate (CRR)

The proportion of patients with complete response(CR) after CT1190B infusion

Time frame
12 months after CT1190B infusion
3

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 frame
12 months after CT1190B infusion
4

Time to response (TTR)

The time from cell infusion to the first assessment of CR or PR

Time frame
12 months after CT1190B infusion

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Kai Hu

Lead sponsor

Beijing GoBroad Hospital

Sponsor institution