This is a phase 2 study to investigate the efficacy and safety of DZD8586 in combination in participants with CLL/SLL. This study consists of two parts: Part A is the safety lead-in phase, and Part B is the dose expansion phase.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
66
DZD8586 will be taken orally once daily on days 1-28 of each cycle.
Venetoclax will be taken orally once daily on days 1-28 starting from cycle 4 day 1.
Anhui Provincial Cancer Hospital
Hefei, Anhui, China
RECRUITINGPeking University Third Hospital
Part A: Incidence of Adverse Events
Time frame: 30 days after the last dose
Part B: 2-year progression free survival (PFS) rate assessed by investigator
Time frame: Approximately 5 years
Part A: PFS assessed by investigator
Time frame: Approximately 5 years
Part A: Objective response rate (ORR) assessed by investigator
Time frame: Approximately 5 years
Part B: ORR assessed by investigator
Time frame: Approximately 5 years
Part B: Incidence of Adverse Events
Time frame: 30 days after the last dose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Beijing, Beijing Municipality, China
Zhujiang Hospital of Southern Medical University
Guangzhou, Guangdong, China
RECRUITINGNanfang Hospital, Southern Medical University
Guangzhou, Guangdong, China
RECRUITINGHenan Cancer Hospital
Zhengzhou, Henan, China
RECRUITINGUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China
RECRUITINGYichang Central People's Hospital
Yichang, Hubei, China
RECRUITINGHunan Cancer Hospital
Changsha, Hunan, China
RECRUITINGThe First People's Hospital of Changzhou
Changzhou, Jiangsu, China
RECRUITINGAffiliated Hospital of Nantong University
Nantong, Jiangsu, China
RECRUITING...and 5 more locations