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A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Zosurabalpin following Intravenous Administration in Healthy Participants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-505411-20-00
Acronym
BP44773
Enrollment
30
Registered
2023-09-12
Start date
2023-09-20
Completion date
2024-03-28
Last updated
2024-03-28

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

Conditions

There is no medical condition being investigated. This is a safety and pharmacokinetic study to be performed in healthy participants.

Interventions

None listed

Sponsors

F. Hoffmann-La Roche AG, F. Hoffmann-La Roche AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Netherlands

Outcome results

None listed

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