Clinical Trials Directory

Trials / Conditions / Hay Fever

Hay Fever

29 registered clinical trials studyying Hay Fever.

StatusTrialSponsorPhase
CompletedImmunological Analysis of Lymph Node Tissue After Intralymphatic Immunotherapy: A Prospective Case Control Stu
NCT05960266
University of ZurichEARLY_Phase 1
CompletedEvaluating the Potential of Large Language Models for Respiratory Disease Consultations
NCT06457269
North Sichuan Medical CollegeN/A
CompletedAudio Data Collection for Identification and Classification of Coughing
NCT04326309
HealthMode Inc.
CompletedMethylprednisolone Injections Treating Birch Pollen Induced Allergic Rhinitis.
NCT04622917
Karolinska InstitutetPhase 4
UnknownClinical Efficacy and Safety of Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced
NCT03724240
ASIT Biotech S.A.Phase 3
CompletedClinical Efficacy and Safety of a Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induc
NCT02560948
BioTech Tools S.A.Phase 3
CompletedSafety, Clinical Tolerability and Immunogenicity of Increasing Doses of gpASIT+TM
NCT02156791
BioTech Tools S.A.Phase 2
CompletedObservational Study With PASCALLERG ® in Patients With Hay Fever
NCT01660737
Pascoe Pharmazeutische Praeparate GmbH
CompletedSafety of gpASIT+TM Subcutaneously Administered to Hay Fever Patients With or Without Immunoregulating Adjuvan
NCT01506375
BioTech Tools S.A.Phase 2
CompletedClinical Efficacy and Safety of gpASIT+TM to Treat Seasonal Allergic Rhinoconjunctivitis
NCT01308021
BioTech Tools S.A.Phase 2
CompletedStudy in Adult and Adolescent Subjects With Seasonal Allergic Rhinitis (SAR)
NCT01024608
Teva Branded Pharmaceutical Products R&D, Inc.Phase 3
CompletedProbiotics for Reduction Of Markers In Subjects With Allergy
NCT01137357
Rijnstate HospitalN/A
CompletedEvaluation of High Speed Laser Doppler Imaging Technology
NCT02619331
Centre Hospitalier Universitaire VaudoisN/A
CompletedEfficacy, Safety and PK of Once or Twice Daily Bilastine (10 or 20 mg) Compared With Placebo in the Symptomati
NCT00574379
Faes Farma, S.A.Phase 2
CompletedPK/PD and Steady State Efficacy Study of Bilastine Compared With Placebo Given Orally in the Treatment of the
NCT00574210
Faes Farma, S.A.Phase 2
CompletedA Study of Ciclesonide Nasal Spray in Patients 18 Years and Older With Seasonal Allergic Rhinitis (BY9010/M1-4
NCT00384475
AstraZenecaPhase 3
CompletedSafety and Efficacy of Ciclesonide in Pediatric Patients (6 to 11 Years of Age) With Seasonal Allergic Rhiniti
NCT00305487
AstraZenecaPhase 3
CompletedSafety and Tolerability of Ciclesonide Nasal Spray in Patients With Perennial Allergic Rhinitis (2-5 Years Old
NCT00261287
AstraZenecaPhase 3
UnknownSafety and Efficacy Study of rEV131 in Allergic Rhinitis
NCT00247520
Evolutec GroupPhase 1 / Phase 2
CompletedStudy Using the Environmental Exposure Unit (EEU) to Assess the Onset of Action of Ciclesonide, Applied as a N
NCT00659503
AstraZenecaPhase 3
CompletedSafety of Ciclesonide Nasal Spray Administered With Inhaled Fluticasone Dipropionate/Salmeterol in Adults With
NCT00163488
AstraZenecaPhase 3
CompletedStudy Using the Environmental Exposure Chamber (EEC) to Assess the Onset of Action of Ciclesonide, Applied as
NCT00659594
AstraZenecaPhase 3
CompletedTo Assess the Safety of Ciclesonide, Applied as a Nasal Spray at Three Dose Levels, in the Treatment of Perenn
NCT00658918
AstraZenecaPhase 3
CompletedSafety and Effectiveness of Ciclesonide Nasal Spray in Children (6 to 11 Years) With Perennial Allergic Rhinit
NCT00163514
AstraZenecaPhase 3
CompletedSafety, Tolerability and Immune Response of IMVAMUNE (MVA-BN)Smallpox Vaccine in Patients With Atopic Disorder
NCT00189917
Bavarian NordicPhase 1
CompletedTo Assess the Safety and Efficacy of Ciclesonide, Applied as a Nasal Spray in the Treatment of Seasonal Allerg
NCT00659841
AstraZenecaPhase 3
CompletedSafety and Effectiveness of Ciclesonide Nasal Spray in Patients With Perennial Allergic Rhinitis During One Ye
NCT00163501
AstraZenecaPhase 3
CompletedOmalizumab (Xolair) and Allergy Shots For the Treatment of Seasonal Allergies
NCT00078195
National Institute of Allergy and Infectious Diseases (NIAID)Phase 2
CompletedRandomized, Double Blind, Parallel Group, Placebo Controlled, Multi-Center Study of the Efficacy and Safety of
NCT02932774
Johnson & Johnson Consumer and Personal Products WorldwidePhase 4