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Clinical trial of cellular immunotherapy for malignant tumor (alpha-beta T cell-based cancer immunotherapy)

Clinical trial of cellular immunotherapy for malignant tumor (alpha-beta T cell-based cancer immunotherapy) - Alpha-beta T cell-based cancer immunotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009420
Enrollment
100
Registered
2012-11-28
Start date
2012-11-12
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

all classes of malignant tumors, after treatment with (or not applicable for) standard therapies for cancers

Interventions

Alpha-beta T cells are intravenously administered almost every two weeks. Minimum dose of each injection will be more than one billion cells.

Sponsors

Center for Advanced Medical Innovation, Kyushu University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients to be included would satisfy all of the following conditions: (1) pathologically diagonized as and informed with malignant tumors, or if patients are diagonized as malignant tumors (such as liver , bile duct and pancreatic cancers) not pathologically but clinically i.e. with diagnostic imaging and laboratory finding, then treated with standard therapy (2) after treatment with (or not applicable for) standard therapies (3) age at the entry into this study is not less than 20 (4) outward patient (5) prognosis at the entry into this study is not less than 3 months and affordable with completion of 1 course immunotherapy (6 times injections) (6) fully informed of the treatment of this study with written consent

Exclusion criteria

Exclusion criteria: Patients to be excluded would satisfy any of the following conditions: (1) T cell- or NK cell-originated leukemia/lymphoma (2) serum positive for HTLV-1 and/or HIV antibody (3) organ- or allogeneic bone marrow-transplant recipients (4) Patients to be or wishing for pregnancy, or breast-feeding (5) Inward patients (6) Patientss who are regarded as inadequate for study enrollment by the investigator

Design outcomes

Primary

MeasureTime frame
Overall survival period (OS) for each class of malignant tumors

Secondary

MeasureTime frame
Progression-free survival period (PFS), Disease-free survival period (DFS), response rate, efficience rate, disease control rate, side effetcs, etc for each class of malignant tumors

Countries

Japan

Contacts

Public ContactTadafumi Iino ( or Shigeo Takaishi )

Center for Advanced Medical Innovation, Kyushu University Division of Advanced Cell Therapy

takaishi@kuhp.kyoto-u.ac.jp092-642-4258

Outcome results

None listed

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