AQUALIS:QoL of CLL Patients Treated With Acalabrutinib in France, Retrospective Study Based on Data From PLATON Database
- Sponsor
- AstraZeneca
- Study ID
- NCT06548152
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Study Details
QoL is often not assessed in real-world studies; hence, there is limited understanding about the real-world QoL of patients diagnosed with CLL. Besides, studies evaluating QoL have largely focused on comparing treated and untreated populations. In particular, QoL of patients treated with acalabrutinib has not been evaluated in a real-life setting. The aim of this study is to describe the QoL of CLL patients treated with acalabrutinib between the treatment initiation and twelve months after, in a real-life setting.
Key Dates
- First listed
- Aug 12, 2024
- Start date
- Apr 28, 2025
- Status verified
- Jul 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 120 participants (estimated)
Primary Outcome Measure
To measure QoL score of CLL patients treated with acalabrutinib, from treatment initiation and up to 12 months [ Time Frame: From treatment initiation and up to 12 months ]
Central Contacts
- AstraZeneca Clinical Study Information Center1-877-240-9479
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