drugset / Trial / NCT05238558

Safety and Immune Response to FMPV-1

NCT05238558

Phase 1 Completed 16 enrolled Hubro Therapeutics AS Quotient Sciences · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a single centre, open-label, non-randomized, Phase I study assessing safety and immune response of FMPV-1 in healthy male subjects.

Timeline

Start
2022-01-31
Primary completion
2022-10-31
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject FMPV-1 Unknown 0.15 mg Intrathecal
Subject FMPV-1 Unknown 0.3 mg Intrathecal
Background sargramostim Protein / enzyme biologic 0.03 mg Intrathecal

Indications