AQUALIS: Quality of Life of Patients With Chronic Lymphocytic Leukemia Treated With Acalabrutinib in France: a Retrospective Observational Study Based on Data Extracted From the PLATON Database

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

⁃ The following patients will be eligible for inclusion in the AQUALIS study :

• Patient enrolled in the PLATON database

• Patient ≥18 years old

• Treatment naïve CLL patient treated with acalabrutinib in a real life setting. Treatment pattern is Acala mono or Acala + Obinutuzumab

• Patient who do not object to his health data collected in PLATON study being re-use for analysis/research purpose

• Patients who started Acala but discontinued before 12 months are also included.

Locations
Other Locations
France
Research Site
RECRUITING
Saint-affrique
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2025-04-28
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 120
Sponsors
Leads: AstraZeneca
Collaborators: Hospitalidee has been asserted to be a valid organization name by UHToulouse, Hospitalidee

This content was sourced from clinicaltrials.gov

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