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Non-interventional Prospective Descriptive Study to Assess the Impact on Patient´s 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
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
HUA - Txagorritxu /ID# 258263
Vitoria-Gasteiz, Alava, Spain
Sant Joan de Deu de Manresa /ID# 258266
Manresa, Barcelona, Spain
Hospital Universitari Mútua Terrassa /ID# 258267
Terrassa, Barcelona, Spain
Hospital Jerez De La Frontera /ID# 258282
Jerez de la Frontera, Cadiz, Spain
Hospital Comarcal de Laredo /ID# 258262
Laredo, Cantabria, Spain
Hospital Universitario Marques de Valdecilla /ID# 258261
Santander, Cantabria, Spain
Hospital Universitario Reina Sofia /ID# 271507
Córdoba, Cordoba, Spain
Hospital Universitario Dr. Negrin /ID# 258285
Las Palmas de Gran Canaria, Las Palmas, Spain
Hospital Universitario de León /ID# 271526
León, Leon, Spain
Hospital Universitario de Fuenlabrada /ID# 258275
Fuenlabrada, Madrid, Spain
Start Date
November 6, 2023
Primary Completion Date
July 1, 2026
Completion Date
July 1, 2026
Last Updated
January 12, 2026
132
ESTIMATED participants
Lead Sponsor
AbbVie
NCT07277231
NCT05006716
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06859424