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Multiple administrations of adoptive T cell therapy in high-risk groups of cancer

A clinical study on the immunological effect of the multiple administrations of adoptive abT cell therapy in high-risk group of cancer

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTc030250451
Enrollment
10
Registered
2025-10-23
Start date
2025-10-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cancer prevention

Interventions

blood collection for cell culture and blood tests. Administration of cultured cells for the treatment 3 times.

Sponsors

Takimoto Rishu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Who meet the following criteria based on a medical checkup conducted within the past six months: - Urinary cell metabolic marker (ALA-PDS) of 3,000 or higher for men and 3,750 or higher for women - No malignant tumors. - No severe liver or kidney dysfunction. - No pathological arrhythmia (2)Have risk factors for cancer and desire for receiving immune-cell therapy. (3)Be > 18 of age when obtaining the informed consent. (4)Be determined to be appropriate by the doctor in charge. (5)Provide written informed consent.

Exclusion criteria

Exclusion criteria: (1)Be diagnosed with cancer. (2)Desire to receive the immune-cell therapy for the treatment of any allergic disease. (3)Be an allotransplant recipient. (4)Have a history or sign of interstitial pneumonia. (5)Have an active autoimmune disease. (6)Have inflammatory bowel syndrome (7)Have sleep apnea syndrome (8)Having diabetes mellitus. (9)Having bowel problems. (10)Be a female who is pregnant, nursing, or of childbearing potential. (11)A subject 70 years of age and above must be carefully considered for the risk of an autoimmune disease to enroll in this study. (12)Receive antibiotics within past 1 month (13)Be determined to be inappropriate by the doctor in charge.

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
Immunological response

Countries

Japan

Contacts

Public ContactTakashi Kamigaki

Koshikai, Non-profit Medical Corporation

citeg@j-immunother.com+81-3-5244-5751

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026