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

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523115-11-00
Acronym
A160_01AD2502
Enrollment
335
Registered
2026-01-09
Start date
2026-01-14
Completion date
Unknown
Last updated
2026-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

and chronic obstructive pulmonary disease, asthma, chronic rhinosinusitis with nasal polyposis, eosinophilic esophagitis, Phase I study in healthy participants. Intended indication: atopic dermatitis, prurigo nodularis

Interventions

None listed

Sponsors

Chong Kun Dang Pharmaceutical Corp.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026