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Surovatamig as Consolidation Therapy in Participants With Chronic Lymphocytic Leukaemia or Small Lymphocytic Lymphoma With Unmutated Immunoglobulin Heavy Chain Variable (IGHV)

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NCT07509151 · readout in 1,836 d

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

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
420estimated
Sites
30
Countries
Australia, Canada, Turkey (Türkiye) +1

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
Start2026-05-05actualWhen the study began enrolling
Primary completion2031-08-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2032-04-05estimatedThe whole study's end, after follow-up
First posted2026-04-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Chronic Lymphocytic Leukaemia or Small Lymphocytic Lymphoma With Unmutated IGHV

Intervention

  • Drug: Surovatamig — also filed as TNB-486, AZD0486

Primary outcomes

what the primary-completion date above is the date OF
DOSRI- Number of participants with adverse events (AEs) and Serious Adverse Events (SAEs)
measured Up to 5 years
Phase III- Progression Free Survival (PFS)
measured Until disease progression or death (up to 5 years)
DOSRI- Number of participants with study intervention discontinuations, dose reductions and dose delays due to AEs
measured Up to 5 years

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