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A Study to Understand How the Study Medicine Dazukibart Works in People With Idiopathic Inflammatory Myopathies

← catalyst calendar

NCT06698796 · readout in 463 d

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
211estimated
Sites
24
Countries
Argentina, Bulgaria, China +9

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
Start2025-01-22actualWhen the study began enrolling
Primary completion2027-11-25estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-11-25estimatedThe whole study's end, after follow-up
First posted2024-11-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Dermatomyositis
  • Polymyositis

Intervention

  • Drug: Dazukibart

Primary outcomes

what the primary-completion date above is the date OF
Treatment-Emergent Adverse Events (AEs), Serious AEs, AEs of Special Interest, and AEs leading to treatment discontinuation
measured 52 weeks
Number of participants with clinically significant laboratory abnormalities
measured 52 weeks
Number of participants with clinically significant abnormalities in vital signs
measured 52 weeks
Number of participants with clinically significant electrocardiogram (ECG) abnormalities
measured 52 weeks
Change from baseline in Forced Vital Capacity (FVC)/Diffusing Capacity of the Lungs for Carbon Monoxide (DLCO)
measured 52 weeks
Absolute values and change from baseline in Columbia-Suicide Severity Rating Scale (C-SSRS)
measured 52 weeks

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