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A study to evaluate how well single and multiple doses of O3R-5671-PRO are tolerated in healthy adult subjects

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522571-28-00
Acronym
O3R-5671-CL-101
Enrollment
88
Registered
2025-08-13
Start date
2025-08-28
Completion date
Unknown
Last updated
2026-01-26

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

Conditions

Inflammatory bowel diseases and psoriasis.

Interventions

None listed

Sponsors

ONCO3R Therapeutics
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Countries

Belgium

Outcome results

None listed

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