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A Study of AZD2962, an IRAK4 Inhibitor (IRAK4 [a Body Protein] Blocker), in Participants With Haematologic Neoplasms (Blood Cancers)

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NCT07064122 · readout in 793 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
72estimated
Sites
21
Countries
Australia, Japan, South Korea +4

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
Start2025-11-03actualWhen the study began enrolling
Primary completion2028-10-20estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-10-20estimatedThe whole study's end, after follow-up
First posted2025-07-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-02actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Haematologic Neoplasms

Intervention

  • Drug: AZD2962

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with dose limiting toxicity (DLT)
measured From Cycle 1 Day 1 up to end of Cycle 1 (28 Days)
Number of participants with Adverse events (AEs) and serious AEs
measured Cycle 1 Day 1 up to safety follow-up (30 days after last dose) (Approximately 3 years)
Duration of exposure
measured Cycle 1 Day 1 up to safety follow-up (30 days after last dose) (Approximately 3 years)
Relative dose intensity
measured Cycle 1 Day 1 up to safety follow-up (30 days after last dose) (Approximately 3 years)

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