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First-in-human study to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of VTX-PID in healthy male volunteers

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-503892-83-00
Acronym
VTX-PID_CLN_001
Enrollment
35
Registered
2023-09-28
Start date
2024-12-27
Completion date
2025-06-28
Last updated
2025-06-04

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

Conditions

Healthy volunteers with circulating Neutralising antibodies (NAbs) against AAV

Interventions

None listed

Sponsors

Vivet Therapeutics
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: May 22, 2026