drugset / Trial / NCT05639166

Study in Adults to Assess the Safety and Efficacy of Inhaled IBIO123, for Post-exposure Prophylaxis of COVID-19

NCT05639166 ↗

Phase 2 Completed 200 enrolled Immune Biosolutions Inc
RandomizedParallel-groupTriple-blindPrevention

Summary

This is a Phase 2, randomized, double-blind, multicentre, placebo-controlled study in adults to assess the safety and efficacy of inhaled IBIO123, for post-exposure prophylaxis of COVID-19. This study aims to evaluate the efficacy and the safety of IBIO123 and the prophylaxis effect of IBIO123 in participants exposed to COVID-19 in the setting of current and uninterrupted household contacts.

Timeline

Start
2023-02-18
Primary completion
2023-05-16
Completion
2023-05-16

Drugs

EvaluationDrugModalityDoseRoute
Subject IBIO123 Monoclonal antibody 10 mg Inhaled

Indications