UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000047806 |
|---|---|
| Receipt number | R000054493 |
| Scientific Title | Sarclisa Specified Drug Use Investigation (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone) (Relapsed or refractory multiple myeloma) |
| Date of disclosure of the study information | 2022/05/26 |
| Last modified on | 2024/05/20 09:54:23 |
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Basic information
Public title
Sarclisa Specified Drug Use Investigation (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone) (Relapsed or refractory multiple myeloma)
Acronym
Sarclisa Specified Drug Use Investigation (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone) (Relapsed or refractory multiple myeloma)
Scientific Title
Sarclisa Specified Drug Use Investigation (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone) (Relapsed or refractory multiple myeloma)
Scientific Title:Acronym
Sarclisa Specified Drug Use Investigation (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone) (Relapsed or refractory multiple myeloma)
Region
| Japan |
Condition
Condition
Relapsed or refractory multiple myeloma
Classification by specialty
| Hematology and clinical oncology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To collect the safety and effectiveness information of use of Sarclisa in Japanese patients with relapsed or refractory multiple myeloma.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Safety (Adverse Drug Reaction)
Key secondary outcomes
Effectiveness
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 will receive Sarclisa (Monotherapy / with Dexamethasone / with Carfilzomib and Dexamethasone).
Key exclusion criteria
NA
Target sample size
86
Research contact person
Name of lead principal investigator
| 1st name | Masahiro |
| Middle name | |
| Last name | TAMURA |
Organization
Sanofi K.K.
Division name
Post-authorization regulatory studies, Medical Affairs
Zip code
163-1488
Address
3-20-2, Nishishinjuku, Shinjuku-ku, Tokyo
TEL
03-6301-3867
Sanofi_Medical@sanofi.com
Public contact
Name of contact person
| 1st name | Public contact for Drug use surveillance |
| Middle name | |
| Last name | - |
Organization
Sanofi K.K.
Division name
Post-authorization regulatory studies, Medical Affairs
Zip code
163-1488
Address
3-20-2, Nishishinjuku, Shinjuku-ku, Tokyo
TEL
03-6301-3867
Homepage URL
Sanofi_Medical@sanofi.com
Sponsor or person
Institute
Sanofi K.K.
Institute
Department
Personal name
Funding Source
Organization
Sanofi 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
Japan Conference of Clinical Research
Address
1-13-23, Minamiikebukuro, Toshima-ku, Tokyo
Tel
03-6868-7022
-
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
| 2022 | Year | 05 | Month | 26 | 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
| 2022 | Year | 01 | Month | 31 | Day |
Date of IRB
| 2022 | Year | 03 | Month | 17 | Day |
Anticipated trial start date
| 2022 | Year | 08 | Month | 19 | Day |
Last follow-up date
| 2025 | Year | 05 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Specified Drug Use Investigation
Management information
Registered date
| 2022 | Year | 05 | Month | 19 | Day |
Last modified on
| 2024 | Year | 05 | Month | 20 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000054493
