UMIN-CTR Clinical Trial

Unique ID issued by UMIN C000000403
Receipt number R000000492
Scientific Title HLA2-3 antigen mismatched stem cell transplantation from related donor
Date of disclosure of the study information 2006/04/12
Last modified on 2017/04/19 09:33:34

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Basic information

Public title

HLA2-3 antigen mismatched stem cell transplantation from related donor

Acronym

HLA2-3 antigen mismatched stem cell transplantation from related donor

Scientific Title

HLA2-3 antigen mismatched stem cell transplantation from related donor

Scientific Title:Acronym

HLA2-3 antigen mismatched stem cell transplantation from related donor

Region

Japan


Condition

Condition

Refractory hematologic malignancies (acute myeloid leukemia, chronic myeloid leukemia, myelodysplastic syndrome, malignant lymphoma, multiple myeloma, severe aplastic anemia)

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

To evaluate the safety and efficacy of HLA 2-3 antigen mismatched stem cell transplantation from related donor for refractory hematologic malignancies

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Phase I,II


Assessment

Primary outcomes

Rate of donor cell engraftment (>90% of donor origin) and incidence of severe GVHD (Phase I)
Disease free survival at 1 year after transplantation (Phase II)

Key secondary outcomes

Incidence and severity of chronic GVHD
Treatment related mortality within 1 year after transplantation
Incidence of infections (bacteria, fungus, virus, etc)
Immune reconstitution after transplantation
GVL effect
Late onset transplantation related complications


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

HLA 2-3 antigen mismatched stem cell transplantation from related donor

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

15 years-old <=

Age-upper limit

45 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Written informed consent.
2) Unavailability of HLA (A, B, DR)-matched or -one antigen mismatched-related donor.
3) Unavailability of HLA (A, B, DR)-matched or one allele of HLA-DRB1 mismatched-unrelated donor or needs urgent transplantation.
4) Availability of HLA 2-3 antigen mismatched related donor.
5) In case of hematologic malignancy in an advanced stage, patients could choose an HLA 2-3 antigen-mismatched donor, even if they have an HLA-matched or -1 antigen-mismatched donor.
6) Sufficient organ function
6-1) Ejection Fraction >= 50%
6-2) serum total billirubin is needed to be less than 2.5 times the normal upper limit
6-3) serum creatinine level <= 1.5* upper limit of institution

Key exclusion criteria

1) Allergy for the agents used in conditioning or GVHD prophylaxis
2) Patients who are considered as inappropriate with other reasons

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroyasu Ogawa

Organization

Hyogo College of Medicine

Division name

Division of Hematology, Department of Internal Medicine

Zip code


Address

1-1, Mukogawa-cho, Nishinomiya city, Hyogo

TEL

0798-45-6886

Email

haplo@hyo-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kazuhiro Ikegame

Organization

Hyogo College of Medicine

Division name

Division of Hematology, Department of Internal Medicine

Zip code


Address

1-1, Mukogawa-cho, Nishinomiya city, Hyogo

TEL

0798-45-6886

Homepage URL


Email

kame@hyo-med.ac.jp


Sponsor or person

Institute

Hyogo College of Medicine

Institute

Department

Personal name



Funding Source

Organization

none

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


Address


Tel


Email



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

2006 Year 04 Month 12 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

Completed

Date of protocol fixation

2006 Year 03 Month 01 Day

Date of IRB


Anticipated trial start date

2006 Year 04 Month 01 Day

Last follow-up date

2016 Year 02 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2006 Year 04 Month 11 Day

Last modified on

2017 Year 04 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000492


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name