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Determine Effectiveness of Anifrolumab In SYstemic Sclerosis (DAISY)

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NCT05925803 · readout in 140 d

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

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
314actual
Sites
150
Countries
Austria, Belgium, Canada +20

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
Start2023-11-08actualWhen the study began enrolling
Primary completion2027-01-06estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-04-05estimatedThe whole study's end, after follow-up
First posted2023-06-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-23actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Systemic Sclerosis
  • Scleroderma

Interventions

  • Combination product: Anifrolumab (blinded) — also filed as Treatment arm (blinded)
  • Drug: Placebo (blinded) — also filed as Placebo arm (blinded)
  • Combination product: Anifrolumab (unblinded, open label) — also filed as Treatment arm (not blinded)

Primary outcome

what the primary-completion date above is the date OF
Number of participants responding to treatment based on the Revised Composite Response Index in Systemic Sclerosis (CRISS-25)
measured at Week 52

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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