Recruiting
Phase 1
Phase 2

AZD0486

Sponsor:

AstraZeneca

Code:

NCT06137118

Conditions

B-cell Acute Lymphoblastic Leukemia (B-ALL)

Eligibility Criteria

Sex: All

Age: 12+

Healthy Volunteers: Not accepted

Interventions

Surovatamig

Study Details

Brief summary:

This is a Phase 1/2, global multicentre, open-label, single-arm, dose escalation and dose optimization study of surovatamig (AZD0486) to evaluate the safety, tolerability, and efficacy of surovatamig (AZD0486) monotherapy in participants with R/R B ALL. The study will consist of 4 parts. Part A: monotherapy dose escalation in 3L+ B-ALL. Part B: dose optimization in 3L+ B-ALL. Part C: Dose expansion in 3L+ B-ALL. Part D: Dose optimization and efficacy expansion in R/R B-ALL (2L+)

Conditions

B-cell Acute Lymphoblastic Leukemia (B-ALL)

Study ID

NCT06137118

Start date

Dec 29, 2023

Status verified date

Aug, 2026

Completion date

Sep 15, 2028

Anticipated

Primary completion date

Feb 11, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 12+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age: 12 years and above (Parts A, B, C and D).
  • Participants with B-cell Acute Lymphoblastic Leukemia with CD19 expression by local lab with:

1. Bone marrow infiltration with >/= 5% blasts
2. Either relapsed or refractory after a minimum of 2 prior therapies or after 1 prior line of therapy if no SOC available option (Parts A, B, C); or relapsed or refractory to ≥1 prior line of therapy (Part D).
3. Philadelphia positive participants are allowed in all parts of the study, if intolerant or refractory to TKIs.
  • For participants older than 16 years, Eastern Cooperative Oncology Group (ECOG) Performance Status less than or equal to 2. For Participants 16 years or younger, Lansky score more or equal to 50%.

The above is a summary, other inclusion criteria details may apply.

Exclusion Criteria:

  • Active CNS involvement by B-ALL, defined by presence of ALL blasts in CSF (CNS2 and CNS3 criteria), or signs of CNS involvement.
  • Isolated extramedullary disease relapse.
  • Testicular leukemia
  • History or presence of clinically relevant CNS pathology such as epilepsy, seizure, paresis, aphasia, stroke, severe brain injuries, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis; or prior Grade 4 neurotoxicity with CAR-T or TCE therapy.
  • History of other malignancy (with certain exceptions).
  • Unresolved AEs >/= Grade 2, from prior therapies
  • Prior therapy with ADCs within 3 weeks, TCEs within 4 weeks, CAR T-cell therapy or autologous HSCT within 8 weeks or prior alloSCT within 12 weeks of start of therapy.
  • GVHD requiring immunosuppressive therapy within 3 weeks prior to AZD0486 treatment.

The above is a summary, other exclusion criteria details may apply.

Study Design

Enrollment

255 participants

Anticipated

Allocation

Randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Part A: AZD0486 Dose Escalation

Ascending dose level cohorts of surovatamig (AZD0486) in B-ALL participants aged 12 years and above.

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.

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.

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.

Interventions

Surovatamig

Investigational Product administered via intravenous infusion.

Primary outcome measure

  • Part A: Frequency of DLTs [ Time Frame: Up to 28 days ]
  • Parts A & B: Safety Evaluation of AZD0486 [ Time Frame: From signing of informed consent through data cutoff, up to 57 months ]
  • Parts B & C: Rate of CR within 3 cycles [ Time Frame: Up to three cycles of 28 days each ]
  • Part D: CR/CRh within 3 cycles [ Time Frame: Up to three cycles of 28 days each ]

Central Contacts and Locations

Central contacts

AstraZeneca Clinical Study Information Center

1-877-240-9479information.center@astrazeneca.com

Locations

Research Site

Recruiting

Duarte, California, United States, 91010

Research Site

Recruiting

Los Angeles, California, United States, 90048

Research Site

Recruiting

Palo Alto, California, United States, 94304

Research Site

Recruiting

Tampa, Florida, United States, 33612

Research Site

Recruiting

Atlanta, Georgia, United States, 30322

Research Site

Recruiting

Chicago, Illinois, United States, 60637

Research Site

Recruiting

New York, New York, United States, 10016

Research Site

Recruiting

Houston, Texas, United States, 77030

Research Site

Recruiting

Richmond, Virginia, United States, 23298

Research Site

Recruiting

Milwaukee, Wisconsin, United States, 53226

More Information

Sponsor

AstraZeneca

Last update posted

Aug 19, 2026

Last verified

Aug, 2026

Keywords

  • B-cell acute lymphoblastic leukemia
  • Leukemia
  • B-lymphocytes
  • Surovatamig
  • AZD0486

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by AstraZeneca on 2026-08-19.