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A Study to Assess Change in Functioning and Health Related Quality of Life in Adult Participants With Chronic Lymphocytic Leukemia (CLL) Receiving Oral Treatments in Routine Clinical Practice in Spain - Trial NCT06125795

Access comprehensive clinical trial information for NCT06125795 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 132 participants.

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NCT06125795
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Trial Details
ClinicalTrials.gov โ€ข NCT06125795
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A Study to Assess Change in Functioning and Health Related Quality of Life in Adult Participants With Chronic Lymphocytic Leukemia (CLL) Receiving Oral Treatments in Routine Clinical Practice in Spain
Non-interventional Prospective Descriptive Study to Assess the Impact on Patientยดs Well-being of Fixed-time Duration (FTD) and Continuous Oral Regimens for Newly Diagnosed and Relapsed/Refractory (R/R) Chronic Lymphocytic Leukemia (CLL) in Routine Clinical Practice in Spain

Study Focus

Observational

Sponsor & Location

AbbVie

Granada,Madrid,Madrid,Madrid,Sevilla, Spain

Timeline & Enrollment

N/A

Nov 06, 2023

Apr 30, 2025

132 participants

Primary Outcome

Change in Participant Functioning Measured Using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) with the EORTC Chronic Lymphocytic Leukemia 17 (EORTC-CLL17) Supplement,Change in Participant Health-related Quality of Life (HRQoL)Measured Using the EORTC QLQ-C30 with the EORTC-CLL17 Supplement

Summary

Chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world. Since in
 most cases CLL remains an incurable disease, the goals of therapy are 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 Spain.
 
 Study participants will receive oral treatments for CLL as prescribed by their study doctor
 in accordance with approved local label. Adult participants prescribed various treatments
 will be enrolled. Around 132 participants will be enrolled in the study in sites in Spain.
 
 Participants will receive oral treatments for CLL according to the approved local label. The
 overall study duration will be 18 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

Chronic lymphocytic leukaemia of B-cell type
Chronic myelomonocytic leukaemia
Acute myelomonocytic leukaemia
Lymphoid leukaemia
Chronic leukaemia of unspecified cell type

Data Source

ClinicalTrials.gov

NCT06125795

Non-Device Trial