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A Study to Evaluate the Efficacy and Safety of DNTH103 in Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CAPTIVATE)

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NCT06858579 · readout in 865 d

Sponsored by Dianthus Therapeutics (industry) · DNTH — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
256estimated
Sites
188
Countries
Argentina, Australia, Belgium +26

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
Start2025-02-10actualWhen the study began enrolling
Primary completion2028-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-12-31estimatedThe whole study's end, after follow-up
First posted2025-03-05actualWhen 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

  • Chronic Inflammatory Demyelinating Polyneuropathy

Interventions

  • Drug: Claseprubart — also filed as DNTH103
  • Drug: Claseprubart — also filed as DNTH103
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Part B: Time From First Dose to Relapse as Assessed by the Adjusted Inflammatory Neuropathy Cause and Treatment (INCAT)
measured Part B baseline to Part B end of treatment period (up to Week 52)

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