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NCT06104293

Determination of Grass Pollen Allergen Concentration Inducing Rhinoconjunctivitis Symptoms in Subjects Allergic to Grass Pollen in ALYATEC Allergen Exposure Chamber

Completed NA Last updated 27 November 2023
What this trial tests

NA trial testing Grass Pollen Allergen Exposure in Allergic Rhinitis Due to Grass Pollen in 24 participants. Completed in 6 April 2023.

Timeline
16 November 2022
Primary endpoint
7 February 2023
6 April 2023

Quick facts

Lead sponsorAlyatec
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposeother
Enrollment24
Start date16 November 2022
Primary completion7 February 2023
Estimated completion6 April 2023
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Alyatec

Who can join

Adults 18 to 65, any sex, with Allergic Rhinitis Due to Grass Pollen. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to determine the optimal concentration of grass pollen allergens inducing rhinoconjunctivitis in subjects allergic to grass pollen in ALYATEC allergen exposure chamber. Four concentrations of grass pollen allergen (Phl p 5) are tested during 3-hour exposures: 0, 30, 60 and 90 ng/m3.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Allergic Rhinitis Due to Grass Pollen

Currently open trials in the same condition.

Other Alyatec trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06104293.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing