Unique ID issued by UMIN | UMIN000009447 |
---|---|
Receipt number | R000011099 |
Scientific Title | Clinical prospective study to investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy |
Date of disclosure of the study information | 2012/12/01 |
Last modified on | 2014/12/04 11:13:50 |
Clinical prospective study to investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy
Clinical prospective study to investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy
Clinical prospective study to investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy
Clinical prospective study to investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy
Japan |
Malignant tumor (all HLA types)
Medicine in general | Gastroenterology | Hepato-biliary-pancreatic medicine |
Cardiology | Pneumology | Endocrinology and Metabolism |
Hematology and clinical oncology | Nephrology | Surgery in general |
Gastrointestinal surgery | Hepato-biliary-pancreatic surgery | Vascular surgery |
Chest surgery | Endocrine surgery | Breast surgery |
Obstetrics and Gynecology | Dermatology | Oto-rhino-laryngology |
Urology | Oral surgery | Neurosurgery |
Malignancy
NO
To investigate efficacy of WT1 peptide (PepTivator(R))-pulsed dendritic cell vaccination therapy for malignant tumors.
Safety,Efficacy
Pragmatic
Not applicable
Immunological responses
Safety
Efficacy
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Vaccine | Maneuver |
WT1 peptide(PepTivator(R))-pulsed dendritic cells are injected on day0, day14, day28, day42, day56, day70
20 | years-old | <= |
Not applicable |
Male and Female
(1)Patients with histologically confirmed malignant tumors (all HLA types)
(2)Patients who recognized WT1 expression on tumor tissue
(3)Performance Status is 0-2
(4)No serious abnormality in bone marrow, liver, and renal functions
(5)Informed consent has been obtained.
Patients who have:
(1)Pulmonary fibrosis or interstitial pneumonia, or history or predisposition of them
(2)Serious drug allergy
(3)Positive for HIV or HTLV-1
(4)Active autoimmune disease
(5)Continuous systemic administration of steroids
(6)Other cancers
(7)Active infections
(8)Pregnant or lactating
(9)Serious cardiac disease
(10)Any reason why, in the opinion of the investigator, the patient should not participate.
5
1st name | |
Middle name | |
Last name | Takashi Kamigaki |
Seta Clinic Group
Clinical research center
Iidabashi 3-6-5 Kokoro to karada no genki plaza 8F, Chiyoda, Tokyo, 102-0072, Japan
03-5215-0086
1st name | |
Middle name | |
Last name | Hiroshi Ibe |
Seta Clinic Group
Clinical research center
Iidabashi 3-6-5 Kokoro to karada no genki plaza 8F, Chiyoda, Tokyo, 102-0072, Japan
03-5215-0086
scrc@j-immunother.com
Seta Clinic Group
Medinet Co.,Ltd.
Profit organization
NO
瀬田クリニックグループ
2012 | Year | 12 | Month | 01 | Day |
Partially published
Completed
2012 | Year | 09 | Month | 03 | Day |
2012 | Year | 12 | Month | 01 | Day |
AACR 2014/American Asociation for Cancer Research 2014
ISCT 2014/International Society for Cellular Therapy 2014
2012 | Year | 11 | Month | 30 | Day |
2014 | Year | 12 | Month | 04 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011099