JRCT ID: jRCT2080225245
Registered date:25/06/2020
Basic Information
Recruitment status | completed |
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Health condition(s) or Problem(s) studied | |
Date of first enrollment | 23/09/2020 |
Target sample size | 888 |
Countries of recruitment | Asia except Japan,North America,South America,Europe,Oceania,Japan |
Study type | Interventional |
Intervention(s) | investigational material(s) Generic name etc : INN of investigational material : Nivolumab, Ipilimumab Therapeutic category code : 429 Other antitumor agents Dosage and Administration for Investigational material : control material(s) Generic name etc : INN of investigational material : Durvalumab Therapeutic category code : 429 Other antitumor agents Dosage and Administration for Investigational material : |
Outcome(s)
Primary Outcome | efficacy |
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Secondary Outcome | efficacy safety |
Key inclusion & exclusion criteria
Age minimum | >= 18age old |
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Age maximum | Not applicable |
Gender | Both |
Include criteria | |
Exclude criteria |
Related Information
Primary Sponsor | |
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Secondary Sponsor | |
Source(s) of Monetary Support | |
Secondary ID(s) | NCT04026412,JapicCTI-205341 |
Contact
Public contact | |
Name | |
Address | |
Telephone | |
mg-jp-clinical_trial@bms.com | |
Affiliation | |
Scientific contact | |
Name | |
Address | |
Telephone | |
mg-jp-clinical_trial@bms.com | |
Affiliation |