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NCT07358156Active, not recruitingPhase 1

A study to compare the Pharmacokinetics, Pharmacodynamic, Immunogenicity, and Safety of CKD-706 with US-Dupixent®, and EU-Dupixent® in Healthy Adult Participants.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 30 Jul 2026

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
335 (estimated)
First submitted
29 Oct 2025
Start date
14 Jan 2026
Lead sponsor
Chong Kun Dang Pharmaceutical Corp.
EU CT number
2025-523115-11-00

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 335
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Parexel International GmbH
Coordinator of this site? Confirm its status
BerlinGermanyActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.