drugset / Trial / NCT06726863

Pharmacokinetics and Pharmacodynamics of Two Prolonged-release Formulations of Vamifeport in Healthy Adults

NCT06726863 ↗

Phase 1 Completed 22 enrolled CSL Behring
RandomizedSequentialOpen-labelOther

Summary

This is a phase 1, single-center, randomized, open-label study to characterize the pharmacokinetics (PK), pharmacodynamics (PD), and safety of vamifeport after multiple oral administrations of one immediate-release (IR) formulation and after single and multiple oral administrations of two prolonged-release (PR) formulation in healthy adult participants.

Timeline

Start
2024-11-22
Primary completion
2025-01-27
Completion
2025-02-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Vamifeport Small molecule — Oral

Indications

No indication recorded.