Skip to main content
Clinical Trials/JPRN-UMIN000006617
JPRN-UMIN000006617
Completed
未知

Phase I/IIa Study of Adoptive Immunotherapy Comprising 2-Methyl-3-Butenyl-1-Pyrophosphate-Stimulated Gamma Delta T Cells in Patients With PSA biochemical failure after radical prostatectomy. - Phase I/IIa Study of Adoptive Immunotherapy Comprising 2-Methyl-3-Butenyl-1-Pyrophosphate-Stimulated Gamma Delta T Cells in Patients With PSA biochemical failure after radical prostatectomy.

Tokyo Women's Medical University0 sites10 target enrollmentOctober 28, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Tokyo Women's Medical University
Enrollment
10
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 28, 2011
End Date
June 23, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Tokyo Women's Medical University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) No current treatment with any anti\-cancer drugs and androgen depletion therapy. 2\) No hypercalcemia that require medication, No C\-reactive protein with an infectious disease that requires medication, No active infection with hepatitis virus or HIV, No current treatment with steroids, No poorly controlled DM or heart failure or arrhythmia, No autoimmune disease and interstitial pneumonia, No other malignancy, No bone of organ transplant recipient, Not pregnant nor nursing, No mental disorder. 3\) Other patients judged to be ineligible by the attending investigators were also excluded from the study.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Phase II Study of Adoptive Immunotherapy Comprising 2-Methyl-3-Butenyl-1-Pyrophosphate-Stimulated Gamma Delta T Cells, Teceleukin, and Zoledronic acid in Patients With Stage IV Renal Cell CarcinomaCytokine refractory Renal cell carcinoma
JPRN-UMIN000004482Tokyo Women's Medical University35
Unknown
Phase 1
Phase I/II study of adoptive immunotherapy using cytotoxic T cells specific for minor histocompatibility antigen restricted to hematopoietic cells for patients with high-risk leukemia that relapsed following allogeneic hematopoietic stem cell transplantatio1) RAEB, CMML 2) AML or ALL in induction failure or beyond first remission 3) Ph/p190-positive ALL at any stage 4) imatinib-resistant CM
JPRN-C000000162Aichi Cancer Center30
Recruiting
Not Applicable
A Pilot Study of Adoptive Immunotherapy Comprising 2-Methyl-3-Butenyl-1-Pyrophosphate-Stimulated Gamma Delta T Cells in Patients With advanced Renal Cell Carcinomaadvanced Renal cell carcinoma
JPRN-UMIN000016793Tokyo Women's Medical University10
Unknown
Phase 1
Phase I/II study of adoptive immunotherapy using predetermined minor histocompatibility antigen-specific cytotoxic T cells for patients with high-risk leukemia that relapsed following allogeneic hematopoietic stem cell transplantation.1) RAEB, CMML 2) AML or ALL in induction failure or beyond first remission 3) Ph/p190-positive ALL at any stage 4) imatinib-resistant CM
JPRN-C000000161Aichi Cancer Center30
Completed
Phase 1
A phase 1 study of adoptive immunotherapy using autologous RNF43 peptide pulse dendritic cells and RNF43 peptide specifically activated lymphocytes in patients with advanced solid tumorsadvanced solid tumors which already have finished available standard therapies.
JPRN-UMIN000003945Kyushu University Hospital10