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RecruitingLast updated: 29 May 2026

SOUNDTRACK-B: This study is recruiting people with relapsed or refractory B-cell Non-Hodgkin Lymphoma who have had at least two prior lines of treatment to evaluate how safe and effective a new intravenous (IV) medicine isA Modular Phase 2, Single-arm, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of AZD0486 in Participants With Relapsed or Refractory (R/R) B-cell Non-Hodgkin Lymphoma (SOUNDTRACK-B)

Trial purpose

Medical clipboardCancer treatment

Tumor type

Blood Cancers Haematological

Age

People18 - 80

Trial acronym

SOUNDTRACK-B

Clinical summary

Summary

This study is assessing how safe, tolerable and effective a drug called Surovatamig (also known as AZD0486) is in people with relapsed or refractory (R/R) B-cell non-Hodgkin lymphomas who have received at least two prior lines of therapy.

It has two modules: Module 1 for follicular lumphoma (FL) and Module 2 for diffuse large B-cell lymphoma (DLBCL). In both modules, AZD0486 will be administered via IV infusion at the recommended phase 2 dose (RP2D).

 

 

 

 

Conditions

This trial is treating people with follicular lymphoma or diffuse large B-cell lymphoma with CD-19 expression

Eligibility

Inclusion

    1. Aged 18 years old and above
    2. Histologically confirmed relapsed refractory FL (Module 1) and LBCL (Module 2) after at least 2 prior lines of therapy
    3. ECOG performance status 0 to 2
    4. Locally confirmed CD-19 expression in lymphoma cells after progression from last CD 19 directed therapy
    5. FDG-avid disease with at least one bi-dimensionally measurable nodal lesion (defined as > 1.5 cm in its longest dimension), or extranodal lesion (defined as > 1.0 cm in its longest dimension)
    6. Adequate hematological function: ANC ≥ 1000/mm3, platelets

      • 75,000/mm3, hemoglobin ≥ 9 g/dL. Transfusion and/or growth factor are allowed but counts must be stable for at least 72 hours afterwards prior to screening
    7. Adequate liver function: total bilirubin <1.5x ULN, AST/ALT ≤ 3xULN or < 5 × ULN in the presence of lymphoma involvement of the liver
    8. Adequate renal function: creatinine clearance (CrCl) of ≥ 45 mL/min
    9. Adequate cardiac function, defined as left ventricular ejection fraction (LVEF) ≥ 45% by echocardiogram or MUGA

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

Exclusion

      • Diagnosis of CLL, Burkitt lymphoma, or Richter's transformation
      • Active CNS involvement by B-NHL
      • Leukemic presentation of B-NHL
      • History or presence of clinically relevant CNS pathology such as epilepsy, seizure, paresis, aphasia, stroke, severe brain injuries, dementia, neurodegenerative disorder including Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis or other severe mental illness
      • Prior therapy with T-cell engager (TCE) within 8 weeks, autologous Hematopoietic Stem Cell Transplantation (HSCT) within 12 weeks, CAR T- cell therapy within 6 months, or prior allogeneic HSCT within 24 weeks of first dose of surovatamig
      • Requires chronic immunosuppressive therapy
      • Unresolved non hematological AEs ≥ Grade 2 from prior therapies; history of ≥ Grade 3 CRS or neurotoxicity from prior CAR-T or TCE therapy
      • History of major cardiac abnormalities.
      • If female, participant must not be pregnant or breastfeeding.

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

 

Inclusion

  • You have had treatment, but your cancer has come back (relapsed or recurrent).
  • You have had treatment but your cancer has gotten worse or has not responded to the treatment you have been given.
  • You have had a certain type of treatment or surgical procedure.

Exclusion

  • You have certain types of non-cancer medical conditions.
  • You have had certain treatments, surgical procedures or drugs.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

Participating hospitals

Recruiting hospitals

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More information

Trial Identifiers

Information on this page is partially produced from ClinicalTrials.gov, EU Clinical Trials Register *. View further details about this trial on the registry via the links below:

Trial sponsor

AstraZeneca

Scientific Title

A Modular Phase 2, Single-arm, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of AZD0486 in Participants With Relapsed or Refractory (R/R) B-cell Non-Hodgkin Lymphoma (SOUNDTRACK-B)

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