A Study to Assess Frequency of Undetectable Minimal Residual Disease (uMRD) in Adult Participants With Chronic Lymphocytic Leukemia (CLL) Receiving Oral Venetoclax Tablets ± Intravenously (IV) Infused Rituximab in Routine Clinical Practice in Japan - Trial NCT06362044
Access comprehensive clinical trial information for NCT06362044 through Pure Global AI's free database. This phase not specified trial is sponsored by AbbVie and is currently Recruiting. The study focuses on Chronic Lymphocytic Leukemia. Target enrollment is 89 participants.
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Study Focus
Observational
Sponsor & Location
AbbVie
Timeline & Enrollment
N/A
Jun 07, 2023
Dec 31, 2024
Primary Outcome
Percentage of Participants with Undetectable Minimal Residual Disease (uMRD)
Summary
Most cases of Chronic lymphocytic leukemia (CLL) remain an incurable disease with the goal of
 therapy being to improve quality of life and to prolong survival. This study will evaluate
 the participant's related outcomes and experience of CLL in adult participants who are
 treated in the Japan.
 
 Study participants will receive oral treatments of Venetoclax±Rituximab for CLL as prescribed
 by their study doctor in accordance with approved local label. Adult participants prescribed
 various treatments Venetoclax±Rituximab will be enrolled. Around 89 participants will be
 enrolled in the study in sites in Japan.
 
 Participants will receive oral venetoclax tablets ± intravenously (IV) infused rituximab
 treatments for CLL according to the approved local label. The overall study duration will be
 27 months.
 
 There is expected to be no additional burden for participants in this trial. All study visits
 will occur during routine clinical practice.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06362044
Non-Device Trial