MAGE-A4-directed TCR-T in the Treatment Amongst Subjects With Advanced Solid Tumors

NCT06170294 | Recruiting Phase 1

• 1 other identifier: JWTCR001001
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

A single-arm, open-label, dose exploratory study to evaluate the safety, efficacy, and pharmacokinetics of autologous humanized anti-MAGE-A4 T cell receptor-engineered T cell (TCR-T) in advanced solid tumors.

Conditions

Advanced Solid Tumor

Outcome Measures

Primary Outcomes (3)

• Rate of dose-limiting toxicities (DLTs)

  Dose-limiting toxicity (DLT) is defined as an adverse event that occurred within 28 days after JWTCR001 infusion that met any of the following criteria. Any Grade ≥3 non-hematologic toxicity associated with JWTCR001 that has not resolved to Grade ≤2 within 7 days, excluding clinically insignificant abnormalities in laboratory indicators. Grade ≥3 hematological toxicities. Grade ≥3 anaphylaxis. Grade ≥3 infection did not resolve to Grade ≤2 within 7 days after anti-infective treatment. Grade ≥3 autoimmune toxicity during treatment. Grade ≥3 cytokine release syndrome (CRS) during treatment that did not resolve to Grade ≤2 within 72 hours. Grade ≥3 TCR-T cell-associated encephalopathy syndrome/immune effector cell-associated neurotoxicity syndrome (CRES/ICANS) that did not resolve to Grade ≤2 within 72 hours. Grade 5 events of any nonmalignant cause.

  28 days

• Rate and severity of adverse events (AEs) and severe adverse events (SAEs)

  An AE is defined as any unfavorable and unintended sign, symptom, or disease (new or worsening) temporally associated with the use of study therapy, regardless of whether or not a causal relationship with the study therapy can be determined.

  2 years

• Rate and severity of clinically-significant abnormalities in laboratory testings

  Clinically-significant abnormalities in laboratory testings.

  2 years

Secondary Outcomes (8)

• Copy number of the vector transgene of JWTCR001 in peripheral blood

  2 years

• MAGE-A4 specific TCR+ T Cell concentration of JWTCR001 in peripheral blood

  2 years

• Antitumor efficacy-Progression-free survival (PFS)

  2 years

• Antitumor efficacy-Duration of response (DOR)

  2 years

• Antitumor efficacy-Time to response (TTR)

  2 years

Study Arms (1)

TCR-MAGE-A4 T-Cells

EXPERIMENTAL

The subjects enrolled will be sequentially assigned to the corresponding dose level.

Drug: TCR-MAGE-A4 T-Cells

Interventions

TCR-MAGE-A4 T-Cells DRUG

* Preconditioning with fludarabine, cyclophosphamide, based chemotherapy regimen at sub-clinical doses * MAGE-A4-directed T cell receptor-engineered T Cells

Also known as: MAGE-A4-directed T cell receptor-engineered T Cells

TCR-MAGE-A4 T-Cells

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• year-old, male or female
• Voluntarily willing to participate in the study and sign the written informed consent form
• Life expectation ≥12 weeks
• European Cooperative Oncology Group (ECOG) ≤1 at screening, 24 hours prior to apheresis (APH), lymphodepletion (LD), and infusion
• Histologically-confirmed recurrent/metastatic advanced solid tumors
• Radiologically-confirmed progression disease after at least one prior line of systematic treatment and no available standard of care at screening, judged by investigators
• Fresh or formalin-fixed paraffin-embedded (FFPE) samples, immunohistochemistry (IHC)-stained MAGE-A4 positive
• Human leukocyte antigen (HLA)-A\*02 allele matched
• Per response evaluation criteria in solid tumors (RECIST) version 1.1, at least one measurable lesion
• Adequate organ functions
• Adequate venous access for APH
• Non-hematological adverse events induced by previous treatment must have recovered to Grade ≤1 according to Common Terminology Criteria for Adverse Events (CTCAE), except for alopecia and peripheral neuropathy
• Women of childbearing potential must agree to use an effective and reliable contraceptive method during 28 days prior to lymphodepletion to 1 year post infusion; Male patients who have not undergone vasectomy and have sexual activity with women of childbearing potential must agree to the use of a barrier contraceptive method since lymphodepletion to 1 year post infusion, and sperm donation is prohibited during the study
• Women of childbearing potential must have negative serum human chorionic gonadotropin β (β-hCG) test result at screening and 48 hours prior to lymphodepletion

You may not qualify if:

• Pregnant or lactating women
• Human immunodeficiency virus (HIV) serology positive, or active hepatitis B virus (HBV)/hepatitis C virus (HCV)/Syphilis/Tuberculosis/ Coronavirus disease 2019 (COVID-19)
• Central nerve system (CNS) metastasis must have received treatment and been neurologically stable for ≥2 months, not requiring anti-seizure medications and off steroids for ≥ 1 month prior to APH
• Another primary malignancy within 3 years (with some exceptions for completely-resected early-stage tumors)
• Subjects with extensive metastases, or more rapid tumor progression prior to lymphodepletion in comparison to screening, etc. which might not be appropriate for further study treatment judged by the investigators
• Systematic autoimmune disorders requiring long-term systematic treatment
• Previously treated with any genetically engineered modified T cell therapy or other cell and gene therapy (CGT)
• History of organ transplant
• Uncontrolled or active infection within 72 hours prior to screening, APH, LD, or within 5 days prior to infusion
• Subjects with other serious diseases that may restrict them from participating in this study
• Clinically significant CNS disorders, such as epilepsy, stroke, Parkinson disease, etc
• Grade ≥ 2 hemorrhage within 30 days prior to screening, or in need of longterm anticoagulants
• Active digestive ulcer or gastrointestinal (GI) bleeding within 3 months prior to screening
• Not satisfying wash-out period for APH
• Previously allergic or intolerable to JWTCR001 or its components

Sponsors & Collaborators

• Peking University: lead
• Shanghai Ming Ju Biotechnology Co., Ltd.: collaborator

Study Sites (1)

Department of GI Oncology,Peking University Cancer Hospital

Beijing, Beijing Municipality, 100142, China

RECRUITING

Study Officials

• Lin Shen

  Peking University Cancer Hospital & Institute

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Lin Shen

CONTACT

861088196561; linshenpku@163.com

Changsong Qi

CONTACT

861088196561; xiwangpku@126.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: December 6, 2023
• First Posted: December 14, 2023
• Study Start: January 1, 2024
• Primary Completion: December 31, 2025
• Study Completion (Estimated): December 31, 2028
• Last Updated: December 14, 2023

Record last verified: 2023-12

Data Sharing

• IPD Sharing: Will share

Locations

CN (1)