CXCR4 Modified Anti-BCMA CAR T Cells for Multiple Myeloma

Phase 1

Recruiting

• Conditions: Multiple Myeloma
• Interventions: Biological: CXCR4 modified anti-BCMA CAR T cells

• Registration Number: NCT04727008
• Lead Sponsor: Sichuan University

Brief Summary

Multiple myeloma (MM) is an incurable plasma cell cancer that almost all patients eventually relapse despite advancement in treatment strategies. B-cell maturation antigen (BCMA) is a cell surface receptor that expressed primarily by malignant and normal plasma cells. This study aims to evaluate the safety and tolerance CXCR4 modified BCMA CAR T cells in treating standard treatment failed refractory/relapsed multiple myeloma, and will follow dose-escalating cohorts. The efficacy of CXCR4 modified BCMA CAR T will also be investigated.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-11-30
• Study First Submitted QC: 2021-01-25
• Study First Posted: 2021-01-27
• Study Start: 2022-09-21
• Status Verified: 2023-12
• Last Update Submitted: 2023-12-05
• Last Update Posted: 2023-12-12
• Primary Completion: 2025-12-31
• Study Completion: 2025-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

1. Male or female, 18 to 75 years old.
2. The expected survival ≥ 12 week
3. ECOG ≤ 2
4. Patients with multiple myeloma that never achieved MR (minor response) or received ≥ 1 line of standard therapy but tumor relapse
5. The liver and renal function is good/adequate organ function; no uncontrolled or active infectious disease
6. Venous channel is unobstructed, which can meet the needs of intravenous drip; no contraindications of mononuclear cell collection
7. Patients can take effective contraceptive measures during the trial period and 1 year after the infusion
8. Voluntary informed consent is given, agree to follow the trial treatment and visit plan

Exclusion Criteria

1. Patients with other uncontrollable cancer
2. Active hepatitis B, hepatitis C, or HIV infection
3. Other uncontrolled active disease
4. Patients with coronary heart disease, angina pectoris, myocardial infarction, cerebral thrombosis, cerebral hemorrhage or any other severe diseases
5. Patients with uncontrollable hypertension(≥ grade II)
6. Patients with history of uncontrollable mental illness
7. Long-term use of immunosuppressants after organ transplantation (inhaled corticosteroids are excluded)
8. Unstable pulmonary embolism or any arteriovenous embolism 30 days before enrollment;
9. Pregnant or lactating women; Men or women who have a pregnancy plan within a year; The patients cannot guarantee effective contraceptive measures during the trial period;
10. Patients with uncontrollable infectious disease or need systematic treatment within the 14 days of enrollment;
11. Patients had other conditions that were not appropriate for the study determined by the researchers.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
CXCR4 modified anti-BCMA CAR T cell therapy	CXCR4 modified anti-BCMA CAR T cells	CAR T cell therapy

Primary Outcome Measures

Name	Time	Method
Dose limiting toxicities (DLT)	2 years	Dose Limiting Toxicities (DLTs) during the first 28 days after anti-BCMA CAR-T cell administration
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)	24 months

Secondary Outcome Measures

Name	Time	Method
ORR (overall response rate)	3 months，6 months	Proportion of subjects with the best overall response (BOR)
CRR (complete response rate)	3 months	Proportion of subjects with the BOR of sCR+CR at Month 3

Trial Locations

Locations (1)

West China Hospital, Sichuan University; 🇨🇳 Chengdu, Sichuan, China