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Recruiting Phase 1 NCT06728189

NCT06728189 A Clinical Research About CD70-targeted CAR-NKT Cells Therapy in Subjects with Advanced Malignant Solid Tumors

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Clinical Trial Summary
NCT ID NCT06728189
Status Recruiting
Phase Phase 1
Sponsor Peking University Cancer Hospital & Institute
Condition Advanced Malignant Solid Tumors
Study Type INTERVENTIONAL
Enrollment 13 participants
Start Date 2024-11-14
Primary Completion 2026-10-17

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
CAR-NKT Cells treatment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 13 participants in total. It began in 2024-11-14 with a primary completion date of 2026-10-17.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a phase I, open-label, single-arm study conducted to evaluate the efficacy, safety and PK of CGC738 in the treatment of advanced malignant solid tumors. Condition or disease:advanced malignant solid tumors Intervention/treatment:Biological: CD70 CAR-NKT cells Phase:Phase 1

Eligibility Criteria

Inclusion Criteria: 1. Age 18 to 75 years. 2. ECOG 0-1 points. 3. The expected survival time is more than 3 months. 4. Patients with advanced advanced malignant solid tumor confirmed by histology or cytology to be recurrent or metastatic after at least second-line treatment. 5. IHC: CD70 positive. 6. At least one measurable lesion at baseline per RECIST version 1.1. 7. The functions of important organs are basically normal: 8. Pregnancy tests for women of childbearing age shall be negative, Both men and women agreed to use effective contraception. 9. Subjects or their guardians agree to participate in this clinical trial and sign the ICF, indicating that they understand the purpose and procedures of this clinical trial and are willing to participate in the research. Exclusion Criteria: 1. Use of cell therapy within the previous one month. 2. Subjects with other malignant tumors within the past 2 years, except basal or squamous skin cancer, superficial bladder cancer, and breast cancer in situ, have been completely cured and do not need follow-up treatment. 3. Patients with leptomeningeal metastasis or central nervous system metastasis, and definite central nervous system underlying diseases with significant symptoms. 4. Immunotherapy, targeted drug therapy or chemotherapy within 5 drug half-lives within 2 weeks before cell infusion. 5. Active hepatitis B, HIV positive and HCV positive. 6. Active infection or uncontrollable infection. 7. Subjects with NYHA heart failure class ≥2 or hypertension uncontrolled by standard therapy requiring special treatment, previous history of myocarditis, or myocardial infarction within 6 months. 8. Unstable respiratory diseases, including interstitial pneumonia. 9. Uncontrolled ascites and pleural effusion 10. Known to have active or uncontrolled autoimmune diseases, such as Crohns disease, rheumatoid arthritis, systemic lupus erythematosus, etc. . 11. Subjects who are using systemic steroids or steroid inhalers for treatment. 12. Pregnant or lactating female subjects. 13. Other investigators deem it unsuitable to participate in the study.

Contact & Investigator

Central Contact

Xinan Sheng Professor, MD

✉ doctor_sheng@126.com

📞 +86-10-88196348

Frequently Asked Questions

Who can join the NCT06728189 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Advanced Malignant Solid Tumors. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06728189 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06728189 currently recruiting?

Yes, NCT06728189 is actively recruiting participants. Contact the research team at doctor_sheng@126.com for enrollment information.

Where is the NCT06728189 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06728189 clinical trial?

NCT06728189 is sponsored by Peking University Cancer Hospital & Institute. The trial plans to enroll 13 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology