Study to Describe the Management and the Use of Healthcare Resources in Patients With Chronic Lymphocytic Leukemia (CLL) Initiating Venetoclax in Routine Clinical Practice
Study Identifier
P16-489
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete
Results Available
Scientific Result Summary
Available Language(s): English
Study Details
Medical Condition
Study Drug
N/A
Phase
N/A
Sex
Female & Male
Age
18+ years
Protocol Summary
A study to assess the real-life management and use of healthcare resources during the initiation of:
- Venetoclax in combination with rituximab is indicated for the treatment of adult participants with chronic lymphocytic leukemia (CLL) who have received at least one prior therapy.
- Venetoclax in participants with CLL with the deletion of the short arm of chromosome 17 (del\[17p\]) who have received at least 1 prior therapy or participants with CLL without del(17p) who have received at least 1 prior therapy and for whom there are no other available treatment options.
Study Locations
Location
Status
Location
University of Calgary /ID# 166416
Calgary, Alberta, Canada, T2N 4Z6
Status
Not applicable
Location
Cross Cancer Institute /ID# 166417
Edmonton, Alberta, Canada, T6G 1Z2
Status
Not applicable
Location
Jack Ady Cancer Centre /ID# 217491
Lethbridge, Alberta, Canada, T1J 1W5
Status
Not applicable
Location
CancerCare Manitoba /ID# 170751
Winnipeg, Manitoba, Canada, R3E 0V9
Status
Not applicable
Location
The Moncton Hospital /ID# 166043
Moncton, New Brunswick, Canada, E1C 6Z8
Status
Not applicable
Location
QE II Health Sciences Centre /ID# 213548
Halifax, Nova Scotia, Canada, B3H 1V7
Status
Not applicable
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