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Clinical Trials/NCT06144385
NCT06144385
Recruiting
Phase 1

A Phase 1, Single-arm, Open-label, Dose-escalation Study of JWATM204 as T Cell-targeted Immunotherapy in the Treatment Amongst Subjects With Advanced Hepatocellular Carcinoma

Shanghai Ming Ju Biotechnology Co., Ltd.1 site in 1 country20 target enrollmentMarch 24, 2022

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Liver Carcinoma
Sponsor
Shanghai Ming Ju Biotechnology Co., Ltd.
Enrollment
20
Locations
1
Primary Endpoint
Rate of dose-limiting toxicities (DLTs)
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This is a single arm, open-label, dose escalation clinical study to evaluate the safety and efficacy of infused autologous GPC3-directed CAR-T in patients with advanced hepatocellular carcinoma refractory to prior systematic treatments.

Registry
clinicaltrials.gov
Start Date
March 24, 2022
End Date
December 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Shanghai Ming Ju Biotechnology Co., Ltd.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18-75 years-old, male or female
  • Voluntarily willing to participate in the study and sign the written informed consent form
  • Life expectation ≥12 weeks
  • Eastern Cooperative Oncology Group (ECOG) performance status scale ≤1
  • Histologically-confirmed hepatocellular carcinoma (HCC)
  • No benefits from curative surgery or other local therapies are expected at screening, judged by investigators
  • Radiologically-confirmed progression disease after at least one prior line of systematic treatment and limited benefits from current available options for hepatocellular carcinoma are expected at screening, judged by investigators
  • Fresh samples or formalin-fixed paraffin-embedded (FFPE) samples, immunohistochemistry (IHC)-stained GPC-3 positive
  • Per RECIST v1.1, at least one measurable lesion
  • Barcelona Clinic Liver Cancer (BCLC) stage C or B and Child-Pugh ≤7

Exclusion Criteria

  • Active brain metastasis
  • Primary lesion or infused lesions with the longest diameter ≥15 cm, or other potential risk which might not be appropriate for further study treatment judged by the investigator
  • Another primary malignancy within 3 years (with some exceptions for completely-resected early-stage tumors)
  • Systematic autoimmune disorders requiring long-term systematic immunosuppression
  • Previously treated with any genetically engineered modified T-cell therapy nor other cell-gene therapy
  • Active infections of hepatitis C virus (HCV), human immunodeficiency virus (HIV), or syphilis
  • Uncontrolled or active infection at screening, prior to apheresis, 72 hours prior to lymphodepletion or 5 days prior to JWATM204 infusion
  • With severe cardiovascular disease History or presence of clinically-relevant central nervous system (CNS) disorders
  • With clinically-significant CNS disorders
  • Current presence of or previously with hepatic encephalopathy

Outcomes

Primary Outcomes

Rate of dose-limiting toxicities (DLTs)

Time Frame: 28 days

Dose-limiting toxicity (DLT) is defined as an adverse event that occurred within 28 days after JWATM204 infusion that met any of the following criteria. Any grade ≥3 nonhematologic toxicity associated with JWATM204 that has not resolved to ≤ grade 2 within 7 days, excluding clinically insignificant abnormalities in laboratory indicators Hematologic toxicity 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 CAR-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.

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

Time Frame: 2 years

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.

Rate and severity of clinically-significant abnormalities in laboratory testings

Time Frame: 2 years

Clinically-significant abnormalities in laboratory testings.

Secondary Outcomes

  • Disease Control Rate (DCR)(2 years)
  • Copy number of the vector transgene of JWATM204 in peripheral blood(1 year)
  • Objective response rate (ORR)(2 years)
  • Progression-free survival (PFS)(2 years)
  • Overal survival (OS)(2 years)

Study Sites (1)

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