UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000015634 |
|---|---|
| Receipt number | R000018170 |
| Scientific Title | Phase I study of EBV specific CTL generated from third party for treatment of EBV associated lymphoproliferative disorder after allogeneic stem cell transplantation |
| Date of disclosure of the study information | 2014/11/07 |
| Last modified on | 2023/11/14 12:44:56 |
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Basic information
Public title
Phase I study of EBV specific CTL generated from third party for treatment of EBV associated lymphoproliferative disorder after allogeneic stem cell transplantation
Acronym
EBV specific CTL for treatment of EBV associated LPD after stem cell transplant
Scientific Title
Phase I study of EBV specific CTL generated from third party for treatment of EBV associated lymphoproliferative disorder after allogeneic stem cell transplantation
Scientific Title:Acronym
EBV specific CTL for treatment of EBV associated LPD after stem cell transplant
Region
| Japan |
Condition
Condition
EBV associated lymphoproliferative disorder after allogeneic stem cell transplantation
Classification by specialty
| Hematology and clinical oncology | Pediatrics |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the safety of EBV specific CTL generated from third party for the treatment of EBV associated lymphoproliferative disorder after allogeneic stem cell transplantation
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Phase I
Assessment
Primary outcomes
Incidence of adverse events and graft-versus-host disease
Key secondary outcomes
Monitoring of EBV viral load and EBV specific CTL in peripheral blood
Clinical course of EBV infection
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Maneuver |
Interventions/Control_1
Administration of EBV specific CTL induced and expanded from donor peripheral blood of third party
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1. Prior allogeneic hematopoietic stem cell transplantation
2. HLA-A0201/0206, HLA-A2402 or HLA-1101
3. Rituximab resistant, difficulty in administering rituximab or CD20 negative EBV associated lymphoproliferative disorder
4. Written informed consent from patient or legal representative
5. Fulfill all of the following criteria:
Performance status 0-3, GOT /GPT =<10 x upper normal limit (UNL), total bilirubin =<3 x UNL,
serum creatinine =<3 x UNL, SpO2>=90% (room air)
Key exclusion criteria
1. Severe or uncontrollable bacterial, fungal,and viral (except EBV) infection
2. Uncontrollable GVHD
3. Uncontrollable heart failure
4. Psychoses
5.History of allergic reaction to albumin
Target sample size
9
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Yoshiyuki Takahashi |
Organization
Nagoya University Graduate School of Medicine
Division name
Department of Pediatrics
Zip code
Address
65 Tsurumai-cho, Showa-ku, Nagoya, Aichi
TEL
052-744-2942
ytakaha@med.nagoya-u.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Nobuhiro Nishio |
Organization
Nagoya University Hospital
Division name
Center for Advanced Medicine and Clinical Research
Zip code
Address
65 Tsurumai-cho, Showa-ku, Nagoya, Aichi
TEL
052-744-2942
Homepage URL
nnishio@med.nagoya-u.ac.jp
Sponsor or person
Institute
Nagoya University Graduate School of Medicine,
Department of Pediatrics
Institute
Department
Personal name
Funding Source
Organization
Nagoya University Hospital
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
名古屋大学医学部附属病院（愛知県）
Other administrative information
Date of disclosure of the study information
| 2014 | Year | 11 | Month | 07 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Open public recruiting
Date of protocol fixation
| 2014 | Year | 10 | Month | 10 | Day |
Date of IRB
| 2016 | Year | 01 | Month | 05 | Day |
Anticipated trial start date
| 2014 | Year | 11 | Month | 10 | Day |
Last follow-up date
| 2026 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2014 | Year | 11 | Month | 07 | Day |
Last modified on
| 2023 | Year | 11 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018170
