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A study to learn how vamorolone affects the body, how safe it is and how it moves into, through and out of the body in healthy male participants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-512101-60-00
Acronym
SNT-I-VAM-026
Enrollment
30
Registered
2024-05-06
Start date
2024-06-05
Completion date
2024-07-06
Last updated
2024-05-06

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

Conditions

Phase I study in healthy male volunteers. Intended indication: Duchenne muscular dystrophy and Becker muscular dystrophy

Interventions

None listed

Sponsors

Santhera Pharmaceuticals (Schweiz) AG, Santhera Pharmaceuticals (Schweiz) AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Countries

Germany

Outcome results

None listed

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