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Study of Single and Multiple Doses of PRS-220 Administered by Oral Inhalation in Healthy Subjects

Healthy Clinical Trial

Official title:
A Phase 1, Randomized, Blinded, Placebo Controlled, Single and Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of PRS 220 Administered by Oral Inhalation in Healthy Subjects.

Clinical Trial Summary

A dose escalating study of PRS-220 administered by oral inhalation in healthy subjects

Clinical Trial Description

PRS-220 is a new drug being developed for treatment of idiopathic pulmonary fibrosis (IPF). The main purpose of this study is to investigate the safety, tolerability, pharmacokinetics, and immunogenicity of single and multiple ascending doses of PRS-220 in healthy subjects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05473533
Study type Interventional
Source Pieris Australia Pty Ltd
Contact
Status Completed
Phase Phase 1
Start date October 31, 2022
Completion date August 11, 2023
View Details
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