UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011985
Receipt number R000013069
Scientific Title HLA 2-3 antigen-mismatched stem cell transplantation for refracotry hematologic malignancies
Date of disclosure of the study information 2013/10/10
Last modified on 2022/10/19 17:29:57

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Basic information

Public title

HLA 2-3 antigen-mismatched stem cell transplantation for refracotry hematologic malignancies

Acronym

Haploidentical stem cell transplantation for hematologic malignancies

Scientific Title

HLA 2-3 antigen-mismatched stem cell transplantation for refracotry hematologic malignancies

Scientific Title:Acronym

Haploidentical stem cell transplantation for hematologic malignancies

Region

Japan


Condition

Condition

refractory hematologic malignancies

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To investigate safety and efficacy of HLA haploidentical stem cell trnasplantation for refractory hematologic malignancies

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Survival rate at 100 days after transplantation

Key secondary outcomes



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

Medicine

Interventions/Control_1

fludarabine 30mg/m2 day -11,-10,-9,-8,-7,-6
melphalan 70mg/m2 day -7,-6
(cytarabine 2g/m2 day -11,-10,-9,-8)
TBI 3Gy day -5
ATG 0.5mg/kg day -3
ATG 1mg/kg day -2,-1

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

16 years-old <=

Age-upper limit

65 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Relapse after allogeneic transplantation
2) Lack an avavilable HLA identical or 1 antigen-mismatched related or unrelated donor

Key exclusion criteria

1) With uncontrol diabetes
2) With uncontrol hypertension
3) With active cancer
4) Positive of HBs Ag or HBe Ag
5) Positive of HIV Ab

Target sample size

25


Research contact person

Name of lead principal investigator

1st name Shingo
Middle name
Last name Yano

Organization

Jikei University Hospital

Division name

Clinical Oncology and Hematology

Zip code

105-8461

Address

3-25-8 Nishi Shinbashi Minatoku Tokyo Japan

TEL

03-3433-1111

Email

yano@jikei.ac.jp


Public contact

Name of contact person

1st name Shingo
Middle name
Last name Yano

Organization

Jikei Universtiy Hospital

Division name

Clinical Oncology and Hematology

Zip code

105-8461

Address

3-25-8 Nishi Shinbashi Minatoku Tokyo Japan

TEL

03-3433-1111

Homepage URL


Email

yano@jikei.ac.jp


Sponsor or person

Institute

Jikei University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Jikei University School of Medicne

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Jikei University Ethics Committee

Address

3-25-8 Nishi-Shinbashi Minato-ku

Tel

03-3433-1111

Email

rinri@jikei.ac.jp


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



Other administrative information

Date of disclosure of the study information

2013 Year 10 Month 10 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

Enrolling by invitation

Date of protocol fixation

2013 Year 04 Month 01 Day

Date of IRB

2013 Year 09 Month 01 Day

Anticipated trial start date

2013 Year 09 Month 01 Day

Last follow-up date

2023 Year 10 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 10 Month 07 Day

Last modified on

2022 Year 10 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013069


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name