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A Study of AZD0486 in Subjects With B-Cell Non-Hodgkin Lymphoma

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NCT04594642 · readout in 670 d

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
226actual
Sites
25
Countries
Australia, Japan, South Korea +2

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-03-02actualWhen the study began enrolling
Primary completion2028-06-19estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-06-19estimatedThe whole study's end, after follow-up
First posted2020-10-20actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • B-cell Non Hodgkin Lymphoma
  • Diffuse Large B Cell Lymphoma
  • High-grade B-cell Lymphoma
  • Follicular Lymphoma

Intervention

  • Drug: AZD0486 IV — also filed as TNB-486

Primary outcomes

what the primary-completion date above is the date OF
Incidence of subjects with Dose-limiting toxicities (DLT)
measured 28 days
Incidence of subjects with adverse events (AEs) and/or serious adverse events (SAEs)
measured From screening until 90 Days after end of treatment
Maximum Observed Serum Concentration of AZD0486 (Cmax)
measured 4 Weeks
Area under the concentration versus time curve from time zero to the last quantifiable time point prior to the next dose (AUClast)
measured 4 Weeks
Apparent terminal half-life (t1/2) of AZD0486
measured From screening until 90 Days after end of treatment

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