Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
30

Summary

Conditions
Relapsed or Refractory Acute Myeloid Leukemia (AML)
Type
Interventional
Phase
Phase 1Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: This study is a 3 part, multicenter, open-label, nonrandomized, sequential group, dose-escalation study to assess safety, tolerability,pharmacokinetics and preliminary anti-tumor activity of ascending doses of AZD5991 alone or in combination with venetoclax in subjects with relapsed or refractory hematologic malignancies.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 85 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT03218683
Collaborators
Not Provided
Investigators
Not Provided