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A Study of the Long-term Safety and Efficacy of Danicamtiv in Adults With Symptomatic Genetic and Familial Dilated Cardiomyopathy

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NCT07771465 · readout ≤ 2,295 d

Sponsored by Kardigan, Inc. (industry) · KARD — their whole pipeline →.

Phase
Phase 3
Status
Not yet recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
332estimated
Sites
78
Countries
Belgium, Denmark, France +8

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
StartAug 2026estimatedWhen the study began enrolling
Primary completionNov 2032estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2033estimatedThe whole study's end, after follow-up
First posted2026-08-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-18actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Symptomatic Genetic Dilated Cardiomyopathy (DCM)

Intervention

  • Drug: Danicamtiv

Primary outcomes

what the primary-completion date above is the date OF
Frequency and severity of treatment-emergent adverse events (TEAEs)
measured 61 months
Frequency and severity of adverse events of special interest (AESIs)
measured 61 months
Frequency and severity of serious adverse events (SAEs)
measured 61 months
Frequency and severity of disease-related events (DREs)
measured 61 months
Frequency of abnormal findings from physical examination
measured 61 months
Frequency of abnormal findings from vital signs
measured 61 months
Frequency of abnormal findings from 12-lead electrocardiograms (ECGs)
measured 61 months
Frequency of abnormal findings from clinical laboratory assessments
measured 61 months

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