Drugs / FMXIN002
last change Apr 2026 re-read 9 days ago

FMXIN002

Investigated by
Nasus Pharma

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT07228325 Nov 2025 → Mar 2026 overdue allergic disease, anaphylaxis Nasus Pharma Enrolling by invitation No outcome recorded

News releases announcing trial results or a regulatory action · 4

DateIssuerRelease
2026-02-17 Nasus Pharma Results Nasus Pharma to Present Data Highlighting Superior Nasal Deposition and Stability of Intranasal Epinephrine Powder at AAAAI 2026 nasuspharma.com ↗
FMXIN002 Epinephrine Intranasal Powder Spray is Stable Throughout 3 Freeze-Thaw Cycles
2024-08-07 Nasus Pharma Results Nasus Pharma Announces Ground-Breaking Five Years Stability of its FMXIN002 Nasal Epinephrine Powder for Severe Allergy and Anaphylaxis nasuspharma.com ↗
Epinephrine base was 97.5% at 5 years well within the defined limits (95-105% ICHQ1 ).
2023-12-05 Nasus Pharma Results Nasus Pharma Announces Positive Clinical Results of Recent Phase 2 Study With FMXIN002 Intranasal Epinephrine nasuspharma.com ↗
FMXIN002 demonstrated clear and meaningful advantage both in the pharmacokinetic profile of the first 20 minutes and in the number of patients reaching drug plasma clinical threshold of Epinephrine.
2021-06-23 Nasus Pharma Results Nasus Pharma Announces Positive Results from a Pilot Clinical Study of FMXIN002 Intranasal Powder Epinephrine Spray in nasuspharma.com ↗
The results of the study with FMXIN002 powder intranasal Epinephrine show that it can provide a safer and more effective rescue for the emergency treatment of life- threatening allergic reactions by providing an easy-to-use device and quicker absorption of Epinephrine

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as FMXIN002 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07228325 ↗
Route Intranasal “Single dose of FMXIN002 epinephrine microspheres powder for nasal application, 4.0 mg, at normal conditions.” NCT07228325 ↗