Surovatamig (AZD0486) as Monotherapy in Participants With Relapsed/Refractory (R/R) B-cell NHL
Condition(s) studied
Investigational drug(s) / intervention(s)
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
Primary outcome measure(s)
- Overall response rate (ORR) (central review) — Module 1: from first dose to end of treatment or data cutoff, whichever comes first, assessed up to approximately 24 months. Module 2: from first dose to end of treatment or data cutoff, whichever comes first, assessed up to approximately 12 months.
Overall response summarized via overall response rate (ORR), defined as the proportion of participants achieving either a Partial Response (PR) or Complete Response (CR) based on Lugano 2014 response criteria for non-Hodgkin Lymphoma, as determined by central review
Trial sites (94)
| Facility | City | Region | Status |
|---|---|---|---|
| Research Site | Phoenix | Arizona | Withdrawn |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| Research Site | Jacksonville | Florida | Withdrawn |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| Research Site | Iowa City | Iowa | Withdrawn |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| Research Site | Overland Park | Kansas | Withdrawn |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| Research Site | St Louis | Missouri | Withdrawn |
| Research Site | New Brunswick | New Jersey | Withdrawn |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| Research Site | Pittsburgh | Pennsylvania | Withdrawn |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 Italy
Other trials for the same condition
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 Italy