UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022764
Receipt number R000026225
Scientific Title Analysis of NK cell function in patients with multiple myeloma
Date of disclosure of the study information 2016/06/16
Last modified on 2016/06/16 07:40:23

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Basic information

Public title

Analysis of NK cell function in patients with multiple myeloma

Acronym

MM-NK function

Scientific Title

Analysis of NK cell function in patients with multiple myeloma

Scientific Title:Acronym

MM-NK function

Region

Japan


Condition

Condition

Multiple myeloma

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To analyze the quantitive and qualitative status of NK cells in patients with multiple myeloma

Basic objectives2

Others

Basic objectives -Others

1)The number of NK cells
2)Surface proteins
3)Cytotoxic activities
4)Response to cytokines in NK cells

Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

To analyze the quantitive and qualitative status in patients with multiple myeloma.
1)The number of NK cells
2)Surface proteins
3)Cytotoxic activities
4)Response to cytokines in NK cells

Key secondary outcomes

To evaluate the effect of monoclonal antibodies on NK cells.
1)Proliferation effects
2)Survival effects
3)Cytotoxic activities
To evaluate the effect of NK cells on myeloma cells.
4)Cytotoxic activities of NK cells against myeloma cells
5)Effects of chemotherapy and stem cell transplantation on NK cells


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Newly diagnosed myeloma
Patients (>=20 years old) with symptomatic myeloma defined by IMWG criteria
2. Relapse/Refractory myeloma
Relapse or refractory (defined by IMWG) to induction, stem cell transplantation, consolidation and/or maintenance therapy.
3. Plateau phase of myeloma
Patients who achieved plateau phase after treaments.
4. Healthy donor (>=20 years old) with written informed concent.

Key exclusion criteria

1)Who does not agree with the participation into the study.
2)Who can not understant the explanation about this study.
3)Who should be excluded judged by principal investigator.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shotaro Hagiwara

Organization

National Center for Global Health and Medicine

Division name

Division of Hematology

Zip code


Address

1-21-1Toyama, Shinjuku, Tokyo

TEL

+81-3-3202-7181

Email

shagiwar@hosp.ncgm.go.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shotaro Hagiwara

Organization

National Center for Global Health and Medicine

Division name

Division of Hematology

Zip code


Address

1-21-1Toyama, Shinjuku, Tokyo

TEL

+81-3-3202-7181

Homepage URL


Email

shagiwar@hosp.ncgm.go.jp


Sponsor or person

Institute

Division of Hematology
National Center for Global Health and Medicine

Institute

Department

Personal name



Funding Source

Organization

National Center for Global Health and Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


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

国立国際医療研究センター


Other administrative information

Date of disclosure of the study information

2016 Year 06 Month 16 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

2016 Year 04 Month 19 Day

Date of IRB


Anticipated trial start date

2016 Year 05 Month 16 Day

Last follow-up date

2021 Year 03 Month 31 Day

Date of closure to data entry

2021 Year 03 Month 31 Day

Date trial data considered complete

2021 Year 03 Month 31 Day

Date analysis concluded

2021 Year 03 Month 31 Day


Other

Other related information

Data not published


Management information

Registered date

2016 Year 06 Month 16 Day

Last modified on

2016 Year 06 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026225


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name