UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000037488 |
|---|---|
| Receipt number | R000042738 |
| Scientific Title | Special Drug Use Results Survey for the use of Symtuza in pregnant women |
| Date of disclosure of the study information | 2019/07/26 |
| Last modified on | 2020/03/06 17:56:22 |
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Basic information
Public title
Special Drug Use Results Survey for the use of Symtuza in pregnant women
Acronym
Special Drug Use Results Survey for the use of Symtuza in pregnant women
Scientific Title
Special Drug Use Results Survey for the use of Symtuza in pregnant women
Scientific Title:Acronym
Special Drug Use Results Survey for the use of Symtuza in pregnant women
Region
| Japan |
Condition
Condition
HIV/AIDS
Classification by specialty
| Infectious disease |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To collect and review information on factors affecting safety, such as setting of occurrence of adverse events under actual use conditions, and effects on infant in patients with HIV infection receiving Symtuza during pregnancy.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Safety (ADR)
Effectiveness(Changes in HIV-RNA level, Changes in CD4 lymphocyte count)
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 with HIV infection, who receive Symtuza during pregnancy and whose outcome of pregnancy can be confirmed.
Key exclusion criteria
NA
Target sample size
3
Research contact person
Name of lead principal investigator
| 1st name | Toshiya |
| Middle name | |
| Last name | Kato |
Organization
Janssen Pharmaceutical K.K.
Division name
Safety Risk Management Dept.
Zip code
101-0065
Address
5-2, Nishikanda 3-chome, Chiyoda-ku, Tokyo
TEL
03-4411-5017
tkato1@its.jnj.com
Public contact
Name of contact person
| 1st name | Masayuki |
| Middle name | |
| Last name | Takagishi |
Organization
Janssen Pharmaceutical K.K.
Division name
Safety Risk Management Dept.
Zip code
101-0065
Address
5-2, Nishikanda 3-chome, Chiyoda-ku, Tokyo
TEL
03-4411-5464
Homepage URL
mtakagis@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
Self funding
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, Nishikanda 3-chome, Chiyoda-ku, Tokyo
Tel
03-4411-5104
mtakagis@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
| 2019 | Year | 07 | 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
| 2019 | Year | 06 | Month | 20 | Day |
Date of IRB
| 2019 | Year | 06 | Month | 20 | Day |
Anticipated trial start date
| 2019 | Year | 07 | Month | 26 | Day |
Last follow-up date
| 2026 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
NA
Management information
Registered date
| 2019 | Year | 07 | Month | 25 | Day |
Last modified on
| 2020 | Year | 03 | Month | 06 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042738
