Observational Study to Monitor Safety and Effectiveness of Obinutuzumab in Follicular Lymphoma or Previously Untreated Chronic Lymphocytic Leukemia
- Conditions
- Chronic Lymphocytic LeukemiaFollicular Lymphoma
- Interventions
- Biological: obinutuzumab
- Registration Number
- NCT03374137
- Lead Sponsor
- Hoffmann-La Roche
- Brief Summary
This study aims to collect clinical data, mainly focused on safety, in the local target population as per the requirement of Korea Ministry of Food and Drug Safety for market authorization. The study population comprises patients with approved local indications chronic lymphocytic leukemia (CLL) and/or follicular lymphoma (FL) in routine clinical practice after launch.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 55
- Administered obinutuzumab under the approved indications in Korea at investigator's discretion
- Previously untreated with obinutuzumab
- Out-of locally approved indications, dosage, and administration
- Pregnant women, breastfeeding women
- Hepatic disease
- Participate in other clinical trials
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description obinutuzumab obinutuzumab Participants with follicular lymphoma or previously untreated chronic lymphocytic leukemia will be treated with obinutuzumab.
- Primary Outcome Measures
Name Time Method Percentage of Participants with Serious Adverse Event (AE)/Adverse Drug Reaction (ADR) from baseline until the end of the participant's observation period (up to approximately 8 years) Percentage of Participants with Unexpected AE/ADR from baseline until end of the participant's observation period (up to approximately 8 years) Percentage of Participants with Expected ADR from baseline until end of the participant's observation period (up to approximately 8 years) Percentage of Participants with Non-serious ADR from baseline until end of the participant's observation period (up to approximately 8 years) Percentage of Participants with AEs of Special Interest (AESIs) from baseline until end of the participant's observation period (up to approximately 8 years)
- Secondary Outcome Measures
Name Time Method Progressive Disease Rate from baseline until end of the participant's observation period (up to approximately 8 years) According to IWCLL 2008 for CLL or Cheson 2014 criteria for FL
Overall Response Rate from baseline until end of the participant's observation period (up to approximately 8 years) According to International Workshop on Chronic Lymphocytic Leukemia (IWCLL) 2008 for CLL or Cheson 2014 criteria for FL
Stable Disease Rate from baseline until end of the participant's observation period (up to approximately 8 years) According to IWCLL 2008 for CLL or Cheson 2014 criteria for FL
Trial Locations
- Locations (17)
Gachon University Gil Medical Center
🇰🇷Incheon, Korea, Republic of
Pusan National University Hospital
🇰🇷Busan, Korea, Republic of
Hallym University Sacred Heart Hospital; Department of Hematology
🇰🇷Gyeonggi-do, Korea, Republic of
St. Vincent's Hospital
🇰🇷Gyeonggi-do, Korea, Republic of
Inje University Busan Paik Hospital; Hematology-oncology
🇰🇷Busan, Korea, Republic of
Catholic Univ. of Incheon St.Mary's Hospital; Hemato-oncology
🇰🇷Incheon, Korea, Republic of
Yonsei University Wonju Severance Christian Hospital
🇰🇷Wonju-Si, Korea, Republic of
Kyung Hee University Hospital
🇰🇷Seoul, Korea, Republic of
Korea University Anam Hospital
🇰🇷Seoul, Korea, Republic of
Seoul St Mary's Hospital
🇰🇷Seoul, Korea, Republic of
Borame Medical Center
🇰🇷Seoul, Korea, Republic of
Yeouido St. Mary's Hospital
🇰🇷Seoul, Korea, Republic of
Samsung Medical Center
🇰🇷Seoul, Korea, Republic of
Seoul National University Hospital
🇰🇷Seoul, Korea, Republic of
ChungAng University Hospital
🇰🇷Seoul, Korea, Republic of
Korea University Guro Hospital
🇰🇷Seoul, Korea, Republic of
The Catholic University of Korea Seoul St. Mary's Hospital
🇰🇷Seoul, Korea, Republic of