UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044074
Receipt number R000050318
Scientific Title Special drug use survey of DARZQURO Combination Subcutaneous Injection (Multiple Myeloma)
Date of disclosure of the study information 2021/06/01
Last modified on 2021/05/17 11:53:56

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Basic information

Public title

Special drug use survey of DARZQURO Combination Subcutaneous Injection (Multiple Myeloma)

Acronym

DRQ1L

Scientific Title

Special drug use survey of DARZQURO Combination Subcutaneous Injection (Multiple Myeloma)

Scientific Title:Acronym

DRQ1L

Region

Japan


Condition

Condition

Multiple Myeloma

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To investigate safety profile of Daratumumab SC under the actual clinical practice in Japan.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Safety(Adverse Drug Reaction)

Key secondary outcomes



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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who have never treated with Darzalex IV and treated with this drug for the first time according to the indication.
Patients who understand the contents of this survey and consent to participate in this survey.

Key exclusion criteria

Patients with a history of the use of Daratumumab.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name MORIYUKI
Middle name
Last name MIYASATO

Organization

Janssen Pharmaceutical K.K.

Division name

Safety Risk Management Dept.

Zip code

101-0065

Address

5-2, Nishi-Kanda 3-chome, Chiyoda-ku, Tokyo

TEL

03-4411-5136

Email

MMIYASAT@its.jnj.com


Public contact

Name of contact person

1st name HIROKAZU
Middle name
Last name SHIRAI

Organization

Janssen Pharmaceutical K.K.

Division name

Safety Risk Management Dept.

Zip code

101-0065

Address

5-2, Nishi-Kanda 3-chome, Chiyoda-ku, Tokyo

TEL

03-4411-5136

Homepage URL


Email

hshirai3@ITS.JNJ.com


Sponsor or person

Institute

Janssen Pharmaceutical K.K.

Institute

Department

Personal name



Funding Source

Organization

Janssen Pharmaceutical K.K.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Janssen Pharmaceutical K.K.

Address

5-2, Nishi-Kanda 3-chome, Chiyoda-ku, Tokyo

Tel

03-4411-5136

Email

kimai4@its.jnj.com


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

2021 Year 06 Month 01 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

Preinitiation

Date of protocol fixation

2021 Year 04 Month 20 Day

Date of IRB


Anticipated trial start date

2021 Year 06 Month 01 Day

Last follow-up date

2023 Year 11 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Nothing in particular


Management information

Registered date

2021 Year 04 Month 28 Day

Last modified on

2021 Year 05 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050318


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name