A Study of AZD0486 Monotherapy or in Combination With Other Anti-Cancer Agents for Mature B-Cell Malignancies
Public ClinicalTrials.gov record NCT06564038. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase I/II Open-Label Multi-Centre Master Protocol to Evaluate the Safety and Efficacy of AZD0486 Monotherapy or in Combination With Other Anticancer Agents in Participants With Mature B-Cell Malignancies
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to assess the safety and efficacy of surovatamig (formerly AZD0486) administered as monotherapy or in combination with other anticancer agents in participants with hematological malignancies
Study identification
- NCT ID
- NCT06564038
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 1, Phase 2
- Enrollment
- 408 participants
Conditions and interventions
Conditions
Interventions
- Surovatamig Drug
- Prednisone (or equivalent) Drug
- Rituximab Drug
- Cyclophosphamide Drug
- Vincristine Drug
- Doxorubicin Drug
- Acalabrutinib Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jan 29, 2025
- Primary completion
- Jun 10, 2029
- Completion
- Jun 10, 2029
- Last update posted
- Aug 11, 2026
2025 – 2029
United States locations
- U.S. sites
- 12
- U.S. states
- 9
- U.S. cities
- 11
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Research Site | Boston | Massachusetts | 02215 | Recruiting |
| Research Site | Hackensack | New Jersey | 07601 | Recruiting |
| Research Site | New Brunswick | New Jersey | 08901 | Recruiting |
| Research Site | New York | New York | 10029 | Recruiting |
| Research Site | New York | New York | 10065 | Withdrawn |
| Research Site | Charlotte | North Carolina | 28204 | Not yet recruiting |
| Research Site | Columbus | Ohio | 43210 | Recruiting |
| Research Site | Portland | Oregon | 97239 | Recruiting |
| Research Site | Philadelphia | Pennsylvania | 19104 | Recruiting |
| Research Site | Pittsburgh | Pennsylvania | 15232 | Recruiting |
| Research Site | Providence | Rhode Island | 02903 | Recruiting |
| Research Site | Houston | Texas | 77030 | Not yet recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 51 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06564038, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 11, 2026 · Synced Sep 2, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06564038 live on ClinicalTrials.gov.