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
Surovatamig
All
255
Interventional
12 Years - n/a
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Part A: AZD0486 Dose Escalation Ascending dose level cohorts of surovatamig (AZD0486) in B-ALL participants aged 12 years and above. | Drug: Surovatamig Investigational Product administered via intravenous infusion. Other Name: AZD0486 |
| 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 years and above, will receive surovatamig (AZD0486) IV infusions and will be randomized in a 1:1 ratio. | Drug: Surovatamig Investigational Product administered via intravenous infusion. Other Name: AZD0486 |
| Experimental: Part C: Dose Expansion Part C will consist of 1 cohort of participants aged 12 years and above, treated with the optimal dose selected in Part B and receive IV surovatamig (AZD0486) monotherapy. | Drug: Surovatamig Investigational Product administered via intravenous infusion. Other Name: AZD0486 |
| Experimental: Part D: Dose Optimization and Efficacy Expansion in 2L+ Part D will enroll participants aged 12 years and above with Ph(+) and Ph(-) B-ALL relapsed/refractory to ≥1 prior line of therapy. Participants will be randomized 1:1 to 2 dose levels of surovatamig IV. | Drug: Surovatamig Investigational Product administered via intravenous infusion. Other Name: AZD0486 |