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Clinical Trials in China / NCT06526793
Recruiting Phase 2

Surovatamig (AZD0486) as Monotherapy in Participants With Relapsed/Refractory (R/R) B-cell NHL

NCT06526793 · tracked via the Priya Life Science China tracker
Sponsor
AstraZeneca
Phase
Phase 2
Started
2024-11-27
Last updated
2026-09-11

Condition(s) studied

B-cell Non-Hodgkin LymphomaFollicular Lymphoma (FL)Large B-Cell Lymphoma (LBCL)

Investigational drug(s) / intervention(s)

Surovatamig

Surovatamig: Investigational Product administered via intravenous infusion.

Study summary

This is a Phase 2 global, multi-center, open-label study to assess the efficacy, safety and tolerability of surovatamig (AZD0486) monotherapy in adult participants with relapsed/refractory B-cell non-Hodgkin lymphoma (NHL) who have received at least two prior lines of therapies. The study has 2 Modules: Module 1 for FL and Module 2 for LBCL.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
1. Key Inclusion Criteria: * Aged 18 years old and above * Histologically confirmed relapsed refractory FL (Module 1) and LBCL (Module 2) after at least 2 prior lines of therapy * ECOG performance status 0 to 2 * Locally confirmed CD-19 expression in lymphoma cells after progression from last CD 19 directed therapy * 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) * 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 * Adequate liver function: total bilirubin \<1.5x ULN, AST/ALT ≤ 3xULN or \< 5 × ULN in the presence of lymphoma involvement of the liver * Adequate renal function: creatinine clearance (CrCl) of ≥ 45 mL/min * 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. 2. Key Exclusion Criteria: * Diagnosis of CLL, Burkitt lymphoma, or Richter's transformation * Active CNS involvement by B-NHL * Leukemic presentation of B-NHL * History of a clinically relevant CNS medical condition or pathology that required treatment in the preceding year, is currently symptomatic, or that the treating investigator considers to have the potential to interfere with the evaluation of safety, such as epilepsy, seizure, paresis, aphasia, stroke, severe brain injuries, dementia, neurodegenerative disorder including Parkinson's disease, cerebellar disease, organic brain syndrome, 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.

Primary outcome measure(s)

Trial sites (94)

FacilityCityRegionStatus
Research Site Phoenix Arizona Withdrawn
Research Site Duarte California Recruiting
Research Site Jacksonville Florida Withdrawn
Research Site Tampa Florida Recruiting
Research Site Chicago Illinois Recruiting
Research Site Iowa City Iowa Withdrawn
Research Site Waukee Iowa Recruiting
Research Site Overland Park Kansas Withdrawn
Research Site Rochester Minnesota Recruiting
Research Site St Louis Missouri Withdrawn
Research Site New Brunswick New Jersey Withdrawn
Research Site New York New York Recruiting
Research Site Charlotte North Carolina Recruiting
Research Site Columbus Ohio Recruiting
Research Site Portland Oregon Recruiting
Research Site Philadelphia Pennsylvania Recruiting
Research Site Pittsburgh Pennsylvania Recruiting
Research Site Pittsburgh Pennsylvania Withdrawn
Research Site Nashville Tennessee Recruiting
Research Site Austin Texas Recruiting
Research Site Houston Texas Recruiting
Research Site San Antonio Texas Not Yet Recruiting
Research Site Milwaukee Wisconsin Recruiting
Research Site Heidelberg Australia Recruiting
Research Site Kogarah Australia Recruiting
Research Site Macquarie University Australia Recruiting
Research Site Nedlands Australia Recruiting
Research Site Porto Alegre Brazil Withdrawn
Research Site São Paulo Brazil Active Not Recruiting
Research Site São Paulo Brazil Active Not Recruiting
Research Site Barrie Ontario Withdrawn
Research Site Brampton Ontario Recruiting
Research Site Ottawa Ontario Recruiting
Research Site Toronto Ontario Recruiting
Research Site Chengdu China Recruiting
Research Site Chengdu China Recruiting
Research Site Guangzhou China Recruiting
Research Site Nanchang China Recruiting
Research Site Nanjing China Recruiting
Research Site Nantong China Recruiting

+ 54 more sites — see the full list on the official registry below.

More AstraZeneca trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06526793 on ClinicalTrials.gov ↗ ← All trials in China