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Pharmacokinetic, Safety, Tolerability, and Immunogenicity Comparison of CKD-704 (risankizumab biosimilar), with EU-approved Skyrizi®, and US licensed Skyrizi® in Healthy Adult Participants

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522345-21-00
Acronym
A148_01PK2408
Enrollment
213
Registered
2025-10-26
Start date
2025-11-11
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Active psoriatic arthritis, Moderately to severely active Crohn’s disease, Moderately to severely active ulcerative colitis, Moderate-to-severe plaque psoriasis

Interventions

None listed

Sponsors

Chong Kun Dang Pharmaceutical Corp.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Poland

Outcome results

None listed

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