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Venetoclax, Cladribine Plus Low-dose Cytarabine for Relapsed/Refractory Philadelphia Chromosome-negative (Ph-) B-cell Acute Lymphoblastic Leukemia (B-ALL): a Single-arm, Multicenter Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to investigate the efficacy and safety of cladribine, venetoclax combined with cytarabine and venetoclax (CAV regimen) for relapsed/refractory (R/R) Philadelphia Chromosome-negative (Ph-) B-cell acute lymphoblastic leukemia (B-ALL).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 15
Maximum Age: 70
Healthy Volunteers: f
View:

• Aged 15-70 years old.

• Patients diagnosed with R/R Ph- B-ALL.

• Patients with ALL must meet one of the following criteria, A or B: A: Refractory ALL disease was defined as follows: (1) failure to attain CR following exposure to at least 1 courses of standard induction therapy; B: Relapsed ALL disease was defined as follows: (1) reappearance of leukemic blasts in the peripheral blood after CR; or (2) detection of ≥ 5% blasts in the BM not attributable to another cause (e.g., BM regeneration after consolidation therapy); or (3) extramedullary relapse.

• ECOG performance status score less than 2.

• Expected survival time ≥ 12 weeks.

• Patients without serious heart, lung, liver, or kidney dysfunction.

• Able to understand and provide informed consent.

Locations
Other Locations
China
The First Affiliated Hospital of Soochow University
RECRUITING
Suzhou
Time Frame
Start Date: 2022-10-01
Estimated Completion Date: 2026-10
Participants
Target number of participants: 36
Treatments
Experimental: CAV regimen
Sponsors
Leads: The First Affiliated Hospital of Soochow University
Collaborators: Northern Jiangsu People's Hospital, Affiliated Hospital of Nantong University, The First Affiliated Hospital of Bengbu Medical University, Jining Medical University, Suzhou Hospital of Traditional Chinese Medicine, The Second People's Hospital of Huai'an

This content was sourced from clinicaltrials.gov

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