Study identifier:D7405C00001
ClinicalTrials.gov identifier:NCT06137118
EudraCT identifier:N/A
CTIS identifier:2023-505840-20-00
A Phase 1/2 Study to Evaluate the Safety and Efficacy of AZD0486 in Adolescent and Adult Participants with Relapsed or Refractory B-Cell Acute Lymphoblastic Leukaemia
B-cell acute lymphoblastic leukemia (B-ALL)
Phase 1/2
No
AZD0486
All
120
Interventional
12 Years - 80 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Oct 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Part A: AZD0486 Dose Escalation Ascending dose level cohorts of AZD0486 in B-ALL participants aged 16-80 years. | Drug: AZD0486 Investigational Product administered via intravenous infusion. Other Name: n/a |
Experimental: Part B: Dose Optimization Up to 2 cohorts will be evaluated prior declared safe-doses and schedules in order to determine the recommended phase 2 dose (RP2D). Participants, aged 12-80 years, will receive AZD0486 IV infusions and will be randomized in a 1:1 ratio. | Drug: AZD0486 Investigational Product administered via intravenous infusion. Other Name: n/a |
Experimental: Part C: Dose Expansion Part C will consist of 1 cohort of participants aged 12-80 years, treated with the optimal dose selected in Part B and receive IV AZD0486 monotherapy. | Drug: AZD0486 Investigational Product administered via intravenous infusion. Other Name: n/a |