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Study details
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A Study of AZD0486 for B-Cell Malignancies

AstraZeneca
NCT IDNCT06564038ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

276

Study length

about 3.1 years

Ages

18+

Locations

12 sites in MA, NC, NJ +6

What this study is about

Researchers are testing the safety and effectiveness of AZD0486, either alone or with other cancer drugs, in people with certain types of lymphoma. The trial will last about 1 year and involve a total of approximately 276 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take AZD0486
  • 2.Take Acalabrutinib
  • 3.Take Cyclophosphamide
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
OralInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

acalabrutinib, cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), doxorubicin (Anthracycline chemotherapy; intercalates DNA and inhibits topoisomerase II), prednisone, rituximab (Monoclonal antibody; targets CD20 on B-cells to destroy them), vincristine

Drug routes

oral (Oral Capsule), infusion, oral

Endpoints

Primary: Number of Participants with Adverse Events, Serious Adverse Events and Adverse Events of Special Interest, Number of Participants with Dose Limiting Toxicity (DLTs)

Secondary: Area Under the Concentration-time Curve (AUC), Clearance (CL) of surovatamig, Complete Response (CR) Rate, Duration of Response (DoR), Half Life (t1/2) of surovatamig, Maximum Observed Concentration (Cmax), Overall Response Rate (ORR), Time to Reach Maximum Concentration (tmax)

Body systems

Oncology