UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000040742
Receipt No. R000046516
Scientific Title Cost-effectiveness analysis of bDMARDs and tsDMARDs in patients with rheumatoid arthritis : Conventional model simulation and alternative approaches based on real world data
Date of disclosure of the study information 2020/06/22
Last modified on 2022/06/06 (Ver. 6)

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Basic information
Public title Cost-effectiveness analysis of bDMARDs and tsDMARDs in patients with rheumatoid arthritis
Acronym Cost-effectiveness analysis of bDMARDs and tsDMARDs in patients with rheumatoid arthritis
Scientific Title Cost-effectiveness analysis of bDMARDs and tsDMARDs in patients with rheumatoid arthritis : Conventional model simulation and alternative approaches based on real world data
Scientific Title:Acronym Cost-effectiveness analysis of bDMARDs and tsDMARDs in patients with rheumatoid arthritis : Conventional model simulation and alternative approaches based on real world data
Region
Japan

Condition
Condition rheumatoid arthritis
Classification by specialty
Clinical immunology Orthopedics
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 Presenting the current cost-effectiveness of bDMARDs / tsDMARDs in Japanese patients with rheumatoid arthritis
Basic objectives2 Others
Basic objectives -Others cost-effectiveness
Trial characteristics_1
Trial characteristics_2
Developmental phase Not applicable

Assessment
Primary outcomes Incremental cost-effectiveness ratio (ICER) after starting treatment with each bDMARDs / tsDMARDs or MTX
Key secondary outcomes

Base
Study type Others,meta-analysis etc

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 -
Key exclusion criteria -
Target sample size

Research contact person
Name of lead principal investigator
1st name Kaori
Middle name
Last name Ouchi
Organization Chugai Pharmaceutical Co.,Ltd.
Division name Medical Science Dept.
Zip code 103-8324
Address 1-1 Nihonbashi-Muromachi 2-Chome,Chuo-Ku Tokyo
TEL 03-3273-0866
Email kondosts@chugai-pharm.co.jp

Public contact
Name of contact person
1st name Satoshi
Middle name
Last name Kondo
Organization Chugai Pharmaceutical Co.,Ltd.
Division name Medical Science Dept.
Zip code 103-8324
Address 1-1 Nihonbashi-Muromachi 2-Chome,Chuo-Ku Tokyo
TEL 03-3273-0866
Homepage URL
Email kondosts@chugai-pharm.co.jp

Sponsor
Institute Chugai Pharmaceutical Co.,Ltd.
Medical Science Dept.
Institute
Department

Funding Source
Organization Chugai Pharmaceutical Co.,Ltd.
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 Non-Profit Organization MINS Institutional Review Board
Address 1-15-14, Dogenzaka, Shibuya, Tokyo, Japan
Tel 03-6416-1868
Email npo-mins@j-irb.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
2020 Year 06 Month 22 Day

Related information
URL releasing protocol N/A
Publication of results Published

Result
URL related to results and publications https://pubmed.ncbi.nlm.nih.gov/35445720/
Number of participants that the trial has enrolled 3262
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
2022 Year 04 Month 21 Day
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description

Progress
Recruitment status Completed
Date of protocol fixation
2020 Year 05 Month 13 Day
Date of IRB
2020 Year 05 Month 27 Day
Anticipated trial start date
2020 Year 07 Month 01 Day
Last follow-up date
2021 Year 12 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information -

Management information
Registered date
2020 Year 06 Month 12 Day
Last modified on
2022 Year 06 Month 06 Day


Link to view the page
URL(English) https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046516