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Study of AZD0120 in Newly Diagnosed Multiple Myeloma Ineligible for ASCT

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NCT07764978 · readout in 876 d

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

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
750estimated
Sites
124
Countries
Australia, Brazil, Canada +12

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
Start2026-06-26actualWhen the study began enrolling
Primary completion2029-01-11estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2034-05-12estimatedThe whole study's end, after follow-up
First posted2026-08-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-14actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Newly Diagnosed Multiple Myeloma

Interventions

  • Biological: AZD0120
  • Biological: Daratumumab
  • Drug: Dexamethasone
  • Biological: Isatuximab
  • Drug: Lenalidomide
  • Drug: Bortezomib
  • Drug: Cyclophosphamide
  • Drug: Fludarabine

Primary outcomes

what the primary-completion date above is the date OF
PFS in NDMM who are ineligible to receive ASCT is measured to demonstrate the superiority of IsaVRd or DRd induction followed by AZD0120 compared to IsaVRd or DRd induction followed by continuous DRd or IsaRd.
measured Up to 9 years.
MRD negative CR rate at 9M in NDMM who are ineligible to receive ASCT is measured to demonstrate the superiority of IsaVRd or DRd induction followed by AZD0120 compared to IsaVRd or DRd induction followed by continuous DRd or IsaRd
measured Up to 9 years.

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