drugset / Trial / NCT07259538

A Phase I Study Evaluating the Safety, Tolerability, and Pharmacokinetics of VVN432 Nasal Spray

NCT07259538 ↗

Phase 1 Recruiting 60 enrolled VivaVision Biotech, Inc
RandomizedSequentialQuadruple-blindTreatment

Summary

The goal of this clinical study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of VVN432 Nasal Spray in healthy volunteers (Phase Ia) and in patients with chronic rhinosinusitis (Phase 1b). This study consists of two parts (Phase 1a and Phase 1b): Phase 1a (SAD) is a single-center, randomized, double-masked, vehicle-controlled study to assess the safety, tolerability, and PK of VVN432 Nasal Spray in healthy adult subjects. Phase 1b (MAD) is a multi-center, randomized, double-masked, vehicle-controlled study to assess the safety, tolerability, PK/PD, and preliminary efficacy of VVN432 Nasal Spray in patients with chronic rhinosinusitis.

Timeline

Start
2025-11-06
Primary completion
2026-07-30
Completion
2026-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject VVN432 Unknown 0.5 % Intranasal
Subject VVN432 Unknown 1 % Intranasal