Skip to content
Study details
Enrolling now

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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take AZD0486
  • 2.Take Acalabrutinib
  • 3.Take Cyclophosphamide
  • +3 more
PhasePhase 1/Phase 2
DrugAcalabrutinib
Routeoral
Primary goalNumber of Participants with Adverse Events, Serious Adverse Events and Adverse Events of Special Interest

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low12%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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