At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Surovatamig (drug)
- How long the study runs
- Study runs about 95 months (dates as stated)
- About the drug or intervention
- Surovatamig — drug: Investigational Product administered via intravenous infusion.
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 270
- Started
- 2024-11-27
- Last checked
- 2026-09
Plain English Summary
What is this study?
- • Testing a new treatment for b-cell non-hodgkin lymphoma
- • Phase2 - 270 participants
- • 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
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with b-cell non-hodgkin lymphoma
Where?
- • London - Research Site
- • Manchester - Research Site
- • Norwich - Research Site
- • Nottingham - Research Site
- • +1 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
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.
More detail
This is a modular, Phase II, multicenter, single-arm, open-label study to evaluate the efficacy and safety of surovatamig (AZD0486) monotherapy administered as an intravenous (IV) infusion in participants with relapsed or refractory B-NHL. The purpose of this study is to determine the efficacy and safety of surovatamig (AZD0486) administered at the RP2D in adults 18 years of age or older with relapsed or refractory B-NHL.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
- How fit you need to be: ECOG 0 or better
What the study is looking for
- ✓Aged 18 years old and above
- ✓confirmed by a biopsy relapsed refractory FL (Module 1) and LBCL (Module 2) after at least 2 previous treatments
- ✓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...
Who cannot take part
- ✗Diagnosis of CLL, Burkitt lymphoma, or Richter's transformation
- ✗Active CNS involvement by B-NHL
- ✗Leukemic presentation of B-NHL
- ✗Requires chronic immunosuppressive therapy
- ✗Unresolved non blood AEs ≥ Grade 2 from prior therapies; history of ≥ Grade 3 CRS or neurotoxicity from...
See the full criteria
Where Is This Study? (5 UK sites)
Research Site
London SE5 9RS, United Kingdom
Research Site
Manchester M20 4BX, United Kingdom
Research Site
Norwich NR4 7UY, United Kingdom
Research Site
Nottingham NG5 1PB, United Kingdom
Research Site
Plymouth PL6 8DH, United Kingdom
How to Get in Touch
AstraZeneca Clinical Study Information Center
Sponsor contactCONTACT
