Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
80

Summary

Conditions
Chronic Lymphocytic Leukemia
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

A Multicenter, Open-Label, Phase 2 study evaluating the efficacy and safety of Acalabrutinib in subjects with relapsed/refractory CLL (N=60) who are intolerant of ibrutinib therapy.

A Multicenter, Open-Label, Phase 2 study evaluating the efficacy and safety of Acalabrutinib in subjects with relapsed/refractory CLL (N=60) who are intolerant of ibrutinib therapy.

Tracking Information

NCT #
NCT02717611
Collaborators
Not Provided
Investigators
Study Director: Acerta Clinical Trials 1-888-292-9613; acertamc@dlss.com