AQUALIS:QoL of CLL Patients Treated With Acalabrutinib in France, Retrospective Study Based on Data From PLATON Database

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAstraZeneca

About this trial

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 criteria

Qualifiers

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

Disqualifiers

Pregnant women

Patients under protection of justice

Patients over the age of 18 and unable to express their non-opposition

Patients with prior CLL treatments

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators

AstraZeneca

Lead sponsor

Hospitalidee

Collaborator

Hospitalidee has been asserted to be a valid organization name by UHToulouse

Collaborator