JRCT ID: jRCT2080223719
Registered date:16/11/2017
Basic Information
Recruitment status | completed |
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Health condition(s) or Problem(s) studied | |
Date of first enrollment | 12/02/2015 |
Target sample size | 200 |
Countries of recruitment | Japan,Asia except Japan,North America,South America,Europe,Oceania |
Study type | Interventional |
Intervention(s) | investigational material(s) Generic name etc : Avelumab INN of investigational material : avelumab Therapeutic category code : 429 Other antitumor agents Dosage and Administration for Investigational material : control material(s) Generic name etc : - INN of investigational material : - Therapeutic category code : Dosage and Administration for Investigational material : - |
Outcome(s)
Primary Outcome | safety efficacy Number of Participants With Confirmed Best Overall Response (BOR) as Per Response Evaluation Criteria in Solid Tumors Version (RECIST) 1.1 |
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Secondary Outcome | safety efficacy Duration of Response According to Response Evaluation Criteria in Solid Tumors Version (RECIST) 1.1 |
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 | Merck Biopharma Co., Ltd. |
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Secondary Sponsor | - |
Source(s) of Monetary Support | Merck KGaA |
Secondary ID(s) | NCT02155647,JapicCTI-173775 |
Contact
Public contact | |
Name | |
Address | |
Telephone | |
MBJ_clinicaltrial_information@merckgroup.com | |
Affiliation | |
Scientific contact | |
Name | |
Address | |
Telephone | |
MBJ_clinicaltrial_information@merckgroup.com | |
Affiliation |