Bioavailability of Nasal Epinephrine

Status Completed

Clinical Trial Summary

A Study to Compare the Bioavailability of Epinephrine following a Single Nasal Dose of FMXIN002 Microspheres Powder with Epinephrine 0.3 mg Intramuscular Injection in Adult Subjects with Seasonal Allergic Rhinitis with and without Nasal Allergen Challenge

Clinical Trial Description

Study Design: Open-label, single-dose, two-period, three-treatment, fixed-sequence, comparative bioavailability study Study Population: Non-smoking, male and female subjects, from 18 to 55 years of age with known history of hay fever, seasonal allergies, or rhinitis during the last year. ;

Study Design

Related Conditions & MeSH terms

Anaphylaxis

Clinical Trial Details

NCT number	NCT04696822
Study type	Interventional
Source	Nasus Pharma
Contact
Status	Completed
Phase	Phase 1
Start date	November 1, 2020
Completion date	September 28, 2021

View Details

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