Actively Recruiting

Early Phase 1
Age: 18Years - 75Years
All Genders
NCT07242417

TC-G203 for Patients With GPC3-Positive Advanced Solid Tumors

Led by Beijing GoBroad Hospital · Updated on 2026-01-21

30

Participants Needed

2

Research Sites

97 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a single-arm, open-label, dose-escalation clinical trial designed to evaluate the safety, tolerability, expansion, and persistence of TC-G203 in patients with GPC3-positive recurrent or metastatic solid tumors who have progressed after prior therapies. The primary objective is to determine the maximum tolerated dose (MTD), with a secondary aim to assess preliminary clinical efficacy in solid tumors.

CONDITIONS

Official Title

TC-G203 for Patients With GPC3-Positive Advanced Solid Tumors

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must voluntarily provide written informed consent.
  • Aged 18-75 years (inclusive).
  • Life expectancy at least 12 weeks.
  • ECOG performance status 0-1.
  • Failed or unsuitable for standard therapy.
  • At least one measurable lesion per RECIST 1.1.
  • GPC3-positive tumor confirmed by immunohistochemistry.
  • Adequate organ and bone marrow function.
  • Effective contraception required for participants of childbearing potential.
  • Adequate venous access for leukapheresis.
Not Eligible

You will not qualify if you...

  • Primary CNS malignancy or uncontrolled CNS metastases.
  • Other malignancies within 5 years.
  • Active autoimmune disease or history of autoimmune disease.
  • Immunodeficiency, including HIV positivity.
  • Bleeding disorders (inherited or acquired).
  • Clinically significant cardiovascular disease.
  • Active infection (including tuberculosis, hepatitis C, syphilis).
  • Pregnant or breastfeeding women.
  • Severe systemic or psychiatric illness.
  • Prior cell or gene therapy.
  • Severe drug hypersensitivity history.
  • Investigator-assessed unsuitability for trial participation.

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Beijing Gobroad Hospital

Beijing, Beijing Municipality, China, 100000

Actively Recruiting

2

GoBroad Healthcare Group

Beijing, Beijing Municipality, China, 102206

Not Yet Recruiting

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Research Team

C

Changsong Qi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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