JAVEMACS: Japan AVElumab Maintenance And Continuous Treatment Study
- Registration Number
- NCT06412848
- Lead Sponsor
- Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
- Brief Summary
This study is a multicenter, non-interventional, retrospective, medical chart review of locally advanced or metastatic (la/m) Urothelial Cancer UC participants who were prescribed avelumab as first line maintenance therapy after a platinum-based chemotherapy. This study aims to understand the index date (i.e., at the initiation of avelumab maintenance therapy) demographics and clinical characteristics of participants with locally advanced/metastatic Urothelial Carcinoma in Japan, and to describe their treatment patterns and outcomes.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 360
- Participants diagnosed with locally advanced/metastatic urothelial carcinoma (la/m UC) before receiving avelumab first line maintenance therapy
- Participants with la/m UC (irrespective of tumor histology) whose disease has not progressed (ongoing stable disease, partial response, or complete response) following completion of first line PBCT and who has been treated with avelumab
- Participants who has been started avelumab first line maintenance therapy for la/m UC from 24 Feb 2021 (date of approval for UC) to 6 months before the date of approval of implementation of this study at each site
- Participants aged >= 18 years old at index date
- Other protocol defined inclusion criteria could apply
- Participant participated in a clinical trial in la/m UC during the study periods.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Urothelial Carcinoma Cohort Avelumab This is a single cohort study enrolling Participants with Urothelial Carcinoma (UC), who are prescribed treatment with avelumab as first line maintenance therapy after a platinum-based chemotherapy (PBCT).
- Primary Outcome Measures
Name Time Method Characteristics of the first line PBCT just prior to avelumab maintenance Up to 3 months Baseline clinical and demographic characteristics Baseline To describe the baseline clinical and demographic characteristics of participants.
- Secondary Outcome Measures
Name Time Method Objective Response Rate (ORR) Up to 3 months Progression-Free Survival (PFS) Up to 3 months Overall Survival (OS) Up to 3 months Time to Treatment Failure (TTF) Up to 3 months Time to Next Treatment (TTNT) Up to 3 months
Related Research Topics
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Trial Locations
- Locations (26)
Iwate Medical University Hospital
🇯🇵Shiwa-gun, Iwate, Japan
Kagawa University Hospital
🇯🇵Kita-gun, Kagawa, Japan
St. Marianna University Hospital
🇯🇵Kawasaki, Kanagawa, Japan
Kindai University Hospital
🇯🇵Osakasayama, Osaka, Japan
Kumamoto University Hospital
🇯🇵Kumamoto, Japan
University Hospital Kyoto Prefectural University of Medicine
🇯🇵Kyoto, Japan
Yamagata University Hospital
🇯🇵Yamagata, Japan
Ehime University Hospital
🇯🇵Toon, Ehime, Japan
Sapporo Medical University Hospital
🇯🇵Sapporo, Hokkaido, Japan
Kurume University Hospital
🇯🇵Kurume, Fukuoka, Japan
Akita University Hospital
🇯🇵Akita, Japan
Teikyo University Hospital
🇯🇵Itabashi-ku, Tokyo, Japan
Saitama Medical University International Medical Center
🇯🇵Hidaka, Saitama, Japan
Juntendo University Hospital
🇯🇵Bunkyo-ku, Tokya, Japan
Kyushu Cancer Center
🇯🇵Fukuoka, Japan
Hirosaki University Hospital
🇯🇵Hirosaki, Aomori, Japan
Nara Medical University Hospital
🇯🇵Kashihara, Nara, Japan
Nippon Medical School Hospital
🇯🇵Bunkyo-ku, Tokyo, Japan
Hokkaido University Hospital
🇯🇵Sapporo, Hokkaido, Japan
Kobe University Hospital
🇯🇵Kobe, Hyogo, Japan
Kyoto University Hospital
🇯🇵Kyoto, Japan
Tokushima University Hospital
🇯🇵Tokushima, Japan
Kitasato University Hospital
🇯🇵Sagamihara, Kanagawa, Japan
National Cancer Center Hospital
🇯🇵Chuo-ku, Tokyo, Japan
Osaka International Cancer Institute
🇯🇵Osaka, Japan
Toyama University Hospital
🇯🇵Toyama, Japan