drugset / Trial / NCT07317960

Phase I Study of PollenVax in Patients With Mugwort Pollen-Induced Allergic Rhinitis

NCT07317960 ↗

Phase 1 Completed 30 enrolled Kazakh National Agrarian University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase I randomized, double-blind, placebo-controlled clinical trial evaluates the safety and tolerability of PollenVax, a novel recombinant allergen-based vaccine for allergen-specific immunotherapy, in adult patients with mugwort pollen-induced allergic rhinitis.

Timeline

Start
2025-11-22
Primary completion
2026-01-16
Completion
2026-01-16

Drugs

EvaluationDrugModalityDoseRoute
Subject PollenVax Vaccine 22 ug Subcutaneous
Subject PollenVax Vaccine 44 ug Subcutaneous

Indications