Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07680257

An Early Clinical Study to Evaluate the Safety and Efficacy of CLDN18.2 CAR T Cell Injection in Subjects With CLDN18.2-Positive Advanced Malignant Solid Tumors

An open label, single/multiple dose exploratory clinical study to evaluate the safety, efficacy, and pharmacokinetics of autologous humanized anti-claudin18.2 chimeric antigen receptor T cell in advanced solid tumor.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

The First Affiliated Hospital Of Anhui Medical University

Hefei, Anhui, 230022, China

Location status: Recruiting

Location contact

Guoping Sun, Cheif Physician

PRINCIPAL_INVESTIGATOR

Huan Zhou

CONTACT

[email protected]

+86 13665527160

Huan Zhou, Professor

PRINCIPAL_INVESTIGATOR

Li Zhang

CONTACT

[email protected]

+86 18655125703

About this study

This study is an open, single/multiple infusion, dose escalation/dose regimen finding study to assess the safety and pharmacokinetics of CAR-CLDN18.2 T cell therapy, and to obtain the preliminary efficacy results in subjects who have been diagnosed with advanced solid tumor with positive claudin 18.2 expression and failed to standard systemic treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Willing to sign the Informed Consent Form (ICF) and comply with predefined visits and related procedures;
  • Age 18 to 75, male or female;
  • Cytology or histology confirmed advanced malignant solid tumors, with moderate to high expression of CLDN18.2;
  • Locally advanced or metastatic solid tumors that are failed of, or refractory to, or contraindicated for standard of care;
  • ECOG PS 0-1;
  • The life expectency ≥ 3 months;
  • Has sufficient organ and bone marrow function.

Exclusion criteria

  • Have active central nervous system metastases or infiltration;
  • Has previously received a bone marrow or organ transplant (including, but not limited to, a liver transplant) or is awaiting a transplant;
  • History of or concurrent other malignancies (cured cervical carcinoma in situ with no recurrence within at least 2 years prior to screening, non-invasive basal cell or squamous cell carcinoma of the skin, locally advanced prostate cancer treated with radical surgery, or post-radical surgery ductal carcinoma in situ may be eligible for the study).
  • Infectious disease;
  • Adverse events caused by prior anti-tumor therapy that have not resolved to grade 1 or baseline, except for alopecia, grade 2 peripheral neuropathy, and stable hypothyroidism with hormone replacement therapy;
  • Have received live attenuated vaccine within one month before screening, or plan to receive live attenuated vaccine during the study;
  • Have major surgery (except liver space-occupying biopsy) within one month before screening, or have planned major surgery during the study.

Treatment and study plan

SUV2208A cell injection

Biological

SUV2208A, DL1, 2 times, Day 0 and Day 28, IV

SUV2208A

Biological

SUV2208A, DL2, 2 times, Day 0 and Day 28, IV

Primary outcomes

  1. DLT

    Time frame: within 24 days from Day 0

    DLT incidence within 24 days after infusion of SUV2208A.

  2. AE/SAE

    Time frame: within 2 years from Day 0

    The incidence, severity, and corelaton of adverse events (AE) and serious adverse events (SAE).

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Celest Therapeutics (Shanghai) Co., Ltd.

Industry

Collaborators

  • The First Affiliated Hospital of Anhui Medical University

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Jul 2, 2026
Registry last updated
Jul 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.