drugset / Trial / NCT05745727

A Study to Evaluate the Safety, Tolerability, PK, and PD Properties of PRX-115 in Adult Volunteers With Elevated Uric Acid Levels

NCT05745727

Phase 1 Completed 64 enrolled Protalix
RandomizedSequentialDouble-blindTreatment

Summary

This is a Phase 1, double-blind, placebo-controlled, single ascending dose study in participants with elevated uric acid levels. This study will be conducted in approximately 64 adult male and female participants in the dose escalation phase.

Timeline

Start
2023-03-23
Primary completion
2024-08-26
Completion
2025-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject PRX-115 Protein / enzyme biologic Intravenous

Indications