| Recruiting | Clinical Study on TQH2722 Injection Combined With Background Therapy for Seasonal Allergic Rhinitis NCT07398859 | Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd. | Phase 2 |
| Not Yet Recruiting | A Study to Evaluate the Efficacy and Safety of AK139 in Participants With Seasonal Allergic Rhinitis NCT07436234 | Akeso | Phase 2 |
| Not Yet Recruiting | A Phase III Study to Assess the Efficacy and Safety of PG-011 Nasal Spray in Adults With Moderate to Severe Se NCT07146126 | Prime Gene Therapeutics Co., Ltd. | Phase 3 |
| Recruiting | Creating A Risk Assessment Tool for Thunderstorm Asthma: the CARISTA Study NCT07055542 | University of Melbourne | N/A |
| Recruiting | A Clinical Study on the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of SHR-1819 Injection in Patie NCT07091357 | Guangdong Hengrui Pharmaceutical Co., Ltd | Phase 2 |
| Completed | Clinical Trial of TQC2938 Injection in Patients With Seasonal Allergic Rhinitis NCT07052097 | Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd. | Phase 2 |
| Recruiting | Phase II/III Seamless Clinical Study of MG-K10 Humanized Monoclonal Antibody Injection in Treatment of Seasona NCT06846385 | Shanghai Mabgeek Biotech.Co.Ltd | Phase 2 / Phase 3 |
| Active Not Recruiting | A Study to Assess the Efficacy and Safety of PG-011 Nasal Spray in Adults With Moderate to Severe Seasonal All NCT06837233 | Prime Gene Therapeutics Co., Ltd. | Phase 2 |
| Completed | Clinical Trial of TQH2722 Injection in Patients With Seasonal Allergic Rhinitis NCT06760182 | Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd. | Phase 2 |
| Completed | Phase II Study of JT002 in the Treatment of Seasonal Allergic Rhinitis in Adults NCT06861101 | Shanghai JunTop Biosciences Co., LTD | Phase 2 |
| Active Not Recruiting | Efficacy and Safety of LP-003 Injection in Patients With Moderate to Severe Seasonal Allergic Rhinitis NCT07291284 | Longbio Pharma | Phase 3 |
| Unknown | Study of CM310 in Subjects With Seasonal Allergic Rhinitis NCT06171074 | Keymed Biosciences Co.Ltd | Phase 2 |
| Recruiting | Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis NCT06300203 | Beijing Tongren Hospital | Phase 2 |
| Completed | Azelastine Allergen Chamber - Onset of Action Study NCT06126952 | MEDA Pharma GmbH & Co. KG | Phase 2 |
| Unknown | A Multicenter, Randomized, Double-blind, Three-arm, Parallel Clinical Endpoint Bioequivalence Study of Monomet NCT06200766 | Zheng Liu ENT | Phase 3 |
| Completed | Efficacy and Safety of LP-003 in Moderate-to-severe Seasonal Allergic Rhinitis Adult NCT06046391 | Longbio Pharma | Phase 2 |
| Terminated | Study to Compare the Pharmacokinetics of Fixed-Dose Combination of Mometasone + Azelastine Nasal Spray to Mome NCT05887843 | Sandoz | Phase 1 |
| Completed | Bioequivalence Study of Azelastine Hydrochloride/ Fluticasone Propionate 137 Microgram/50 Microgram Nasal Spra NCT06180083 | Humanis Saglık Anonim Sirketi | Phase 1 |
| Completed | Efficacy and Safety of Azelastine +Mometasone , Nasal Spray, 140 mcg + 50 mcg, (Sandoz d.d., Slovenia) and Mom NCT05590598 | Sandoz | Phase 3 |
| Completed | A Placebo-controlled Study of 2-day Pre-treatment With Fexofenadine in Seasonal Allergic Rhinitis NCT05692154 | Opella Healthcare Group SAS, a Sanofi Company | Phase 3 |
| Completed | Efficacy and Safety of PQ Grass in Subjects With Seasonal Allergic Rhinitis and/or Rhinoconjunctivitis Induced NCT05540717 | Allergy Therapeutics | Phase 3 |
| Completed | Threshold Concentrations for Ragweed and Birch Pollen in Seasonal Allergic Rhinitis NCT05346718 | Fraunhofer-Institute of Toxicology and Experimental Medicine | N/A |
| Completed | Prospective, Randomized, Multinational, Multicenter, Double-blind, Placebo and Active Controlled Trial in 4 Pa NCT05311475 | Sandoz | Phase 3 |
| Completed | Allergen Challenge Trial of IRL201104 in Seasonal Allergic Rhinitis NCT05098522 | Revolo Biotherapeutics | Phase 2 |
| Recruiting | Acupuncture at the Sphenopalatine Ganglion in the Treatment of Moderate-to-severe Seasonal Allergic Rhinitis NCT04815668 | Guang'anmen Hospital of China Academy of Chinese Medical Sciences | N/A |
| Completed | To Investigate Drug-drug Interaction and Relative Bioavailability Between the FDC AzelastineHCL/Beclomethasone NCT04817800 | Humanis Saglık Anonim Sirketi | Phase 1 / Phase 2 |
| Completed | Biomarkers in Nasal Samples of Seasonal Allergic Rhinitics NCT04670627 | University of North Carolina, Chapel Hill | — |
| Completed | Dymista Allergen Chamber - Onset of Action Study NCT04652245 | MEDA Pharma GmbH & Co. KG | Phase 4 |
| Completed | The Efficacy of Preseasonal Omalizumab Treatment NCT04489121 | Beijing Tongren Hospital | N/A |
| Unknown | The Role of the Nasal Allergen Provocation Test in Starting and Monitoring Allergen Immunotherapy NCT04544774 | Universitaire Ziekenhuizen KU Leuven | — |
| Unknown | Efficacy, Safety and Underlying Mechanisms of Sphenopalatine Ganglion Acupuncture for Seasonal Allergic Rhinit NCT04052945 | Beijing Tongren Hospital | N/A |
| Unknown | Effectiveness of Sodium Hyaluronate In Relieving Nasal Symptoms Of Children With Seasonal Allergic Rhinitis NCT04752956 | Saglik Bilimleri Universitesi | N/A |
| Completed | A Clinical Pharmacology Study of MT-2990 in Seasonal Allergic Rhinitis Patients NCT03570957 | Tanabe Pharma Corporation | Phase 1 |
| Completed | Evaluation of Nasal Inflammatory Biomarkers NCT03450031 | Fraunhofer-Institute of Toxicology and Experimental Medicine | N/A |
| Completed | Study of Efficacy and Safety of Omalizumab in Severe Japanese Cedar Pollinosis Adult and Adolescent Patients NCT03369704 | Novartis Pharmaceuticals | Phase 3 |
| Completed | Effect and Underlying Immunological Mechanisms of Sublingual Immunotherapy in Allergic Rhinitis NCT03649139 | Beijing Tongren Hospital | Phase 3 |
| Completed | A Study of Tolerability and Safety of a New Cumulative Dose of Grass MATA MPL NCT03931993 | Allergy Therapeutics | Phase 1 |
| Completed | MP-AzeFlu Allergen Chamber - Onset of Action Study NCT03004131 | MEDA Pharma GmbH & Co. KG | Phase 4 |
| Unknown | Effectiveness of Bifidobacteria in Children Affected by Seasonal Allergic Rhinitis NCT02807064 | University of Campania Luigi Vanvitelli | Phase 3 |
| Completed | Non-interventional Study to Assess the Tolerability, the Safety Profile and the Adherence of Different Up-dosi NCT03097432 | University Hospital of Cologne | — |
| Completed | Efficacy and Safety of Fixed Dose Combination GSP 301 Nasal Spray (NS) in the Treatment of Seasonal Allergic R NCT02631551 | Glenmark Specialty S.A. | Phase 3 |
| Completed | Psychological Factors That Influence Severity of Allergic Rhinitis NCT04709614 | The University Clinic of Pulmonary and Allergic Diseases Golnik | — |
| Completed | Dose Selection Study of Efficacy and Safety of Different Doses of Grass MATA MPL and Grass MATA Using mEECs™ NCT02582073 | Allergy Therapeutics | Phase 2 |
| Unknown | 4"S" - Seasonal Symptoms Suppression Study NCT02557269 | Association Asthma, Bulgaria | Phase 4 |
| Completed | Allergen Biocube Study Evaluating Efficacy and Safety of Nasapaque Nasal Solution in Adult Subjects With Aller NCT02377895 | 3E Therapeutics Corporation | Phase 1 / Phase 2 |
| Completed | Efficacy and Safety Study of Desloratadine (MK-4117) in Japanese Participants With Seasonal Allergic Rhinitis NCT02320396 | Organon and Co | Phase 3 |
| Completed | To Study GSP 301 in Patients With Seasonal Allergic Rhinitis NCT02318303 | Glenmark Pharmaceuticals Ltd. India | Phase 2 |
| Completed | Efficacy and Safety of SPARC1310 in Seasonal Allergic Rhinitis NCT01940146 | Sun Pharma Advanced Research Company Limited | Phase 2 |
| Completed | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Immunotherapy)-Tablet in Adult Su NCT02245360 | Abbott | Phase 3 |
| Unknown | Clinical Equivalence of Azelastine Hydrochloride and Fluticasone Propionate, 137/50 mcg Nasal Spray to Dymista NCT02249663 | Teva Pharmaceuticals USA | Phase 3 |
| Completed | Comparative Safety and Efficacy of Two Steroid Treatments in the Relief of the Symptoms of Seasonal Allergic R NCT02230696 | Padagis LLC | Phase 3 |
| Completed | Efficacy and Safety of Ciclesonide Nasal Spray in Participants With Seasonal Allergic Rhinitis (SAR) in Russia NCT02155881 | AstraZeneca | Phase 3 |
| Completed | Compliance and Usability Study Evaluating RHINIX™ Nasal Filters NCT02108379 | University of Aarhus | N/A |
| Completed | Study of Grass-SPIRE in Subjects With Grass Allergies and Asthma NCT02161107 | Circassia Limited | Phase 2 |
| Completed | Efficacy Park Study Assessing Rhinix™ Nasal Filters for Hay Fever NCT02108574 | University of Aarhus | N/A |
| Terminated | Clinical Equivalence Study of Fluticasone Propionate Nasal Spray, 50 mcg/Actuation vs. Flonase in Allergic Rhi NCT02246920 | Teva Pharmaceuticals USA | Phase 3 |
| Completed | Efficacy and Safety of Fixed Dose Combination (FDC) of Olopatadine Hydrochloride and Mometasone Furoate Nasal NCT03444506 | Glenmark Pharmaceuticals Ltd. India | Phase 2 |
| Completed | Safety Study of Ragweed-SPIRE in Subjects With Ragweed Allergies and Asthma NCT02061670 | Circassia Limited | Phase 2 |
| Completed | Study to Compare the Therapeutic Equivalence of Mometasone Furoate Nasal Spray, 50 mcg With Nasonex Nasal Spra NCT02125253 | Amneal Pharmaceuticals, LLC | Phase 3 |
| Completed | Evaluating the Efficacy of Ragweed-SPIRE Following Exposure to Ragweed Allergen in an Environmental Exposure C NCT02061709 | Circassia Limited | Phase 2 |
| Unknown | A Study Comparing the Bioequivalence of Azelastine Hydrochloride and Fluticasone Propionate Nasal Spray (Apote NCT02279563 | Apotex Inc. | Phase 2 |
| Completed | Monocenter 6-period Study in Patients With Seasonal Allergic Rhinitis to Birch Pollen to Establish a Challenge NCT01983865 | Fraunhofer-Institute of Toxicology and Experimental Medicine | N/A |
| Terminated | Pilot Study to Evaluate Ear Acupressure Effects in Treating Seasonal Allergic Rhinitis NCT01921348 | University of Mississippi Medical Center | N/A |
| Completed | Safety and Efficacy Trial of Dymista Nasal Spray in Children Ages 4 to 11 With Seasonal Allergic Rhinitis (SAR NCT01915823 | Meda Pharmaceuticals | Phase 3 |
| Completed | Study of the Efficacy and Safety of MK-0476 in Japanese Pediatric Participants With Seasonal Allergic Rhinitis NCT01857063 | Organon and Co | Phase 3 |
| Completed | Post Marketing Surveillance for Contac Bien Z in Japan NCT02020902 | GlaxoSmithKline | — |
| Completed | Clinical Equivalence Study of Mometasone Nasal Spray NCT01850823 | Actavis Inc. | Phase 3 |
| Completed | Bepotastine Besilate Nasal Sprays in the Treatment of Seasonal Allergic Rhinitis (SAR) NCT01753739 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | Allergic Rhinitis Changes the Sinus Microbiome NCT01852513 | University of Chicago | Phase 4 |
| Completed | Assessment of Fluticasone Propionate on Ocular Allergy Symptoms NCT01817790 | GlaxoSmithKline | Phase 3 |
| Completed | Phase II Study Evaluating ONO-4053 and Cetirizine in Subjects With Seasonal Allergic Rhinitis NCT01748344 | Ono Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Evaluation of the Beneficial Effects of a Nasal Spray of Resveratrol in Children With Seasonal Allergic Rhinit NCT02130440 | University of Campania Luigi Vanvitelli | Phase 3 |
| Completed | A Safety and Bioequivalence of a Mometasone Nasal Spray, 50 mcg/Actuation Compared With Nasonex® Nasal Spray 5 NCT01673659 | Padagis LLC | Phase 3 |
| Completed | Combination Study Of S-555739/Cetirizine HCl In Adult Patients With Seasonal Allergic Rhinitis NCT01651871 | Shionogi | Phase 2 |
| Completed | Effect of a Probiotic on Seasonal Allergic Rhinitis Symptoms NCT01653652 | Société des Produits Nestlé (SPN) | N/A |
| Completed | Clinical Equivalence Study of Mometasone Nasal Spray, 50 Mcg/Actuation NCT01523236 | Teva Pharmaceuticals USA | Phase 1 / Phase 2 |
| Completed | Efficacy, Safety, and Tolerability Study of ACT-129968 in Patients With Seasonal Allergic Rhinitis NCT01484119 | Idorsia Pharmaceuticals Ltd. | Phase 3 |
| Completed | Bepotastine Besilate-corticosteroid Nasal Spray Combination Compared to Placebo, Bepotastine Besilate Nasal Sp NCT01578278 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | A Safety and Efficacy Study of Ciclesonide Nasal Aerosol in Subjects 6-11 Years With Seasonal Allergic Rhiniti NCT01458275 | Sumitomo Pharma America, Inc. | Phase 3 |
| Completed | Retrospective Record Review of Adults and Children Advised for Allergen Immunotherapy (MK-7243-022) NCT01549340 | ALK-Abelló A/S | — |
| Completed | Effects of Phenylephrine Extended-Release Tablets on Allergy-Related Nasal Congestion (P08498 AM1) NCT01413958 | Bayer | Phase 3 |
| Completed | Investigate the Safety/Tolerability and Efficacy of Bilastine 20mg in Korean Patients With Seasonal Allergic R NCT01400828 | Yuhan Corporation | Phase 3 |
| Completed | Immune-modulatory Effect of Probiotic Strain on Grass Pollen Allergic Individuals NCT01660698 | Société des Produits Nestlé (SPN) | N/A |
| Completed | Safety and Efficacy of Ectoin Allergy Nasal Spray and Ectoin Allergy Eye Drops in the Treatment of Seasonal Al NCT01342601 | Bitop AG | N/A |
| Completed | Study of an Investigational Nasal Aerosol or Placebo Nasal Aerosol in Children (Ages 6-11) With Seasonal Aller NCT01307319 | Teva Branded Pharmaceutical Products R&D, Inc. | Phase 3 |
| Completed | Trial of STAHIST in Seasonal Allergic Rhinitis NCT01293201 | Magna Pharmaceuticals, Inc. | Phase 3 |
| Completed | A Study Comparing The Bioequivalence Of Ciclesonide Nasal Spray (Apotex, Inc.) To That Of Omnaris™ Nasal Spray NCT02273817 | Apotex Inc. | Phase 3 |
| Completed | Rhinitis, Cognition and Driving Performance NCT01318681 | Maastricht University Medical Center | N/A |
| Completed | Reduction of IgE Antibody in Human Allergic Subjects NCT01280149 | Northwestern University | Phase 1 |
| Completed | Proof of Activity Study of UR-63325 in Allergic Rhinitis Induced by Nasal Challenge NCT01260753 | Palau Pharma S.L.U. | Phase 2 |
| Completed | Safety and Efficacy of Bepotastine Besilate Nasal Spray in the Treatment of Seasonal Allergic Rhinitis NCT01277341 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | Study of ACT-129968 in Adult Patients With Seasonal Allergic Rhinitis NCT01241214 | Idorsia Pharmaceuticals Ltd. | Phase 2 |
| Completed | Vienna Challenge Chamber Study Using RV658 in Subjects With Allergic Rhinitis NCT01230619 | Respivert Ltd | Phase 2 |
| Completed | Clinical Trial of STAHIST in Seasonal Allergic Rhinitis (SAR) Subjects NCT01171664 | Magna Pharmaceuticals, Inc. | Phase 2 |
| Terminated | Prospective Observational Study of Concomitant Allergic Rhinitis Treatment Patterns Among Patients Starting on NCT01337323 | GlaxoSmithKline | — |
| Completed | Vitamin D Plus Fluticasone Propionate NCT01103934 | University of Chicago | Phase 4 |
| Completed | Safety, Pharmacokinetics, and Efficacy of Bepotastine Besilate Nasal Product After Ragweed Pollen Exposure in NCT01222299 | Bausch & Lomb Incorporated | Phase 1 / Phase 2 |
| Completed | Eosinophil Markers and Development of Disease in Allergic Rhinitis NCT01192386 | University of Aarhus | — |
| Completed | Fluticasone Furoate Treatment of Daytime Somnolence and Cognitive Performance in Seasonal Allergic Rhinitis NCT00997620 | Western Sky Medical Research | Phase 4 |
| Completed | A Single and Multiple Dose Study to Explore the Safety of JNJ-38224342 in Healthy Patients and Patients With S NCT01054352 | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | Phase 1 |
| Completed | Study in Adult and Adolescent Subjects With Seasonal Allergic Rhinitis (SAR) NCT01024608 | Teva Branded Pharmaceutical Products R&D, Inc. | Phase 3 |
| Completed | Clinical Trial to Assess the Efficacy and Safety of Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol for the NCT01010971 | Sumitomo Pharma America, Inc. | Phase 3 |
| Completed | Effect of Veramyst and Olopatadine 0.2% Opthalmic Solution on Allergy Symptoms NCT01007253 | University of Chicago | Phase 4 |
| Completed | A Study to Determine the Capacity of VAK694 When Combined With Allergen Immunotherapy to Bring About Specific NCT01018693 | Novartis Pharmaceuticals | Phase 2 |
| Completed | AUTO-ACUSAR - Effects of Acupuncture on the Autonomic Nervous System in Seasonal Allergic Rhinitis Patients NCT01271595 | Charite University, Berlin, Germany | N/A |
| Completed | Consumer Preference Study of Two Formulations of Phenylephrine Hydrochloride (Study CL2008-15)(P07530)(COMPLET NCT00976209 | Bayer | Phase 3 |
| Completed | The Effect of Nasal Carbon Dioxide (CO2) Used As-Needed in the Symptomatic Treatment of Seasonal Allergic Rhin NCT00917020 | Capnia, Inc. | Phase 2 |
| Completed | The Effect of Nasal Carbon Dioxide (CO2) in the Symptomatic Treatment of Seasonal Allergic Rhinitis NCT00917111 | Capnia, Inc. | Phase 2 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00883168 | Meda Pharmaceuticals | Phase 3 |
| Completed | Comparison of Seasonal Allergic Rhinitis Treatment With 2 Antihistamines Used in Combination With Intranasal C NCT00845195 | Alcon Research | Phase 4 |
| Completed | Study to Assess the Efficacy and Safety of BDP HFA Nasal Aerosol in Patients 12 Years and Older With SAR NCT00854360 | Teva Branded Pharmaceutical Products R&D, Inc. | Phase 2 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00824473 | Meda Pharmaceuticals | Phase 3 |
| Completed | Clinical Trial to Assess the Efficacy and Safety of Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol for the NCT00790023 | Sumitomo Pharma America, Inc. | Phase 3 |
| Completed | A Study to Compare the Efficacy of QAV680 Against Placebo in Treating Seasonal Allergic Rhinitis in an Environ NCT00784732 | Novartis | Phase 2 |
| Completed | A Study Evaluating the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00740792 | Meda Pharmaceuticals | Phase 3 |
| Completed | The Effect of Nasal Carbon Dioxide (CO2) in the Treatment of Seasonal Allergic Rhinitis NCT00688441 | Capnia, Inc. | Phase 2 |
| Completed | Subcutaneous Immunotherapy Treatment for Patients With Hypersensitivity to Grass Pollen NCT00916422 | Laboratorios Leti, S.L. | Phase 3 |
| Completed | Study of the Effect of SCH 900538 on Congestion in Subjects With Seasonal Allergic Rhinitis (Study P05031)(COM NCT00673062 | Merck Sharp & Dohme LLC | Phase 2 |
| Completed | A Randomized, Double-blind, Placebo-controlled Study on the Effect of CVT-E002 in Patients With Seasonal Aller NCT00726401 | Afexa Life Sciences Inc | Phase 2 |
| Completed | Comparison of Olopatadine 0.6% and Fluticasone Proprionate 50mcg Nasal Sprays in a Two Week Seasonal Allergic NCT00691665 | Alcon Research | Phase 4 |
| Completed | Acupuncture for Seasonal Allergic Rhinitis NCT00610584 | Charite University, Berlin, Germany | N/A |
| Completed | Can a Nasal Decongestant Test Predict Treatment Outcomes in Seasonal Allergic Rhinitis? NCT00618332 | University of Chicago | N/A |
| Completed | A Study Evaluating the Efficacy and Impact on Health-related Quality of Life of Levocetirizine in Adults With NCT00653224 | UCB Pharma | Phase 4 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00651118 | Meda Pharmaceuticals | Phase 3 |
| Completed | A Study Evaluating the Efficacy and Impact on Health-related Quality of Life of Levocetirizine in Adults With NCT00621959 | UCB Pharma | Phase 4 |
| Completed | Compare Captisol-Enabled (CE) Budesonide + Azelastine Nasal Solution and Rhinocort Aqua + Astelin in an Enviro NCT00940953 | Ligand Pharmaceuticals | Phase 2 |
| Completed | MOA Study of Ze 339 in Seasonal Allergic Rhinitis NCT00862225 | Max Zeller Soehne AG | Phase 2 |
| Completed | Safety and Efficacy Study of Epinastine Nasal Spray in Subjects With Seasonal Allergic Rhinitis (P08648) NCT00564421 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00660517 | Meda Pharmaceuticals | Phase 3 |
| Completed | A Study to Evaluate the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00660829 | Meda Pharmaceuticals | Phase 3 |
| Completed | Efficacy, 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 |
| Completed | A Randomized, Placebo Controlled Study to Determine the Efficacy and Speed of a Nasal Spray in Allergen Induce NCT00561717 | Bayer | Phase 4 |
| Completed | PK/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 |
| Completed | Efficacy and Safety of Sublingual Tablets of Grass Pollen Allergen Extract NCT00619827 | Stallergenes Greer | Phase 1 |
| Completed | Safety and Efficacy of Olopatadine HCl Nasal Spray in 6-11 Year Old Patients NCT00578929 | Alcon Research | Phase 3 |
| Completed | A Study to Evaluate the Safety and Efficacy of Two Nasal Sprays to Treat Seasonal Allergies NCT00720278 | Meda Pharmaceuticals | Phase 3 |
| Completed | A Study to Evaluate the Safety & Effectiveness of a Nasal Spray to Treat Seasonal Allergies NCT00719862 | Meda Pharmaceuticals | Phase 3 |
| Completed | Effect of a Nasal Bolus Allergen Challenge on Inflammatory Markers NCT00483353 | Pfizer | Phase 1 |
| Completed | Study of Mometasone Furoate Nasal Spray and Oxymetazoline Nasal Spray Given Together Once A Day To Treat Seaso NCT00552110 | Organon and Co | Phase 2 |
| Completed | Efficacy and Safety of Lectranal® in Treatment of Seasonal Allergic Rhinitis Symptoms NCT00460538 | Milsing d.o.o. | Phase 4 |
| Completed | Intranasal Steroids and the Nasal Ocular Response NCT00473915 | University of Chicago | Phase 4 |
| Unknown | Comparison of the Effect of Montelukast and Cetirizine on Allergic Inflammation in Children With Allergic Rhin NCT00488176 | Medical University of Lodz | Phase 4 |
| Completed | Placebo-Controlled Study of Mometasone Furoate Nasal Spray (MFNS) 200 mcg QD in the Treatment of Seasonal Alle NCT00468312 | Organon and Co | Phase 3 |
| Completed | Regulatory Lymphocytes in Patients Treated With Specific Immunotherapy NCT01475188 | Ministry of Science and Higher Education, Poland | Phase 4 |
| Completed | Montelukast as a Controller of Atopic Syndrome NCT00559546 | University of Helsinki | Phase 4 |
| Completed | A Study To Investigate If MRI Scanning Is Effective At Seeing What Hayfever Drugs Do In Nasal Passage. NCT00517946 | GlaxoSmithKline | — |
| Completed | Placebo-Controlled Study of Mometasone Furoate Nasal Spray (MFNS) 200 mcg Once Daily (QD) in the Treatment of NCT00453063 | Organon and Co | Phase 3 |
| Completed | This Study Contains an Active Drug Treatment Group With Mometasone Furoate Nasal Spray and a Placebo (Dummy) T NCT00491504 | Organon and Co | Phase 4 |
| Completed | Compare CE-Budesonide Nasal Solution & Rhinocort Aqua in an EEC Study of AR NCT00938613 | Ligand Pharmaceuticals | Phase 2 |
| Completed | Trial With Allergic Rhinitis Patients Taking GSK256066 Versus Placebo In A Pollen Challenge Chamber NCT00430157 | GlaxoSmithKline | Phase 2 |
| Completed | Effects of Imatinib in Subjects With Seasonal Allergic Rhinitis and Who Are Sensitive to Timothy Grass Pollen NCT00426179 | Novartis | Phase 1 / Phase 2 |
| Completed | A Study of Epinastine Nasal Spray in Subjects With Seasonal Allergic Rhinitis NCT00407927 | Merck Sharp & Dohme LLC | Phase 2 |
| Completed | Effect of Loratadine/Montelukast Combination on Congestion in SAR Patients Exposed to Pollen in an EEU (Study NCT00423995 | Organon and Co | Phase 3 |
| Completed | Phase I/IIa Study on Chitin Microparticles in Subjects Suffering From Allergic Rhinitis NCT00443495 | CMP Therapeutics Ltd | Phase 1 / Phase 2 |
| Completed | A Randomized, Double-Blind, 4-way Crossover Study to Evaluate the Efficacy of Bilastine in the Vienna Challeng NCT00420082 | Faes Farma, S.A. | Phase 2 |
| Completed | Pilot Study of Allergy Immunotherapy and Prevention of Viral Respiratory Infections NCT00405899 | West Penn Allegheny Health System | — |
| Completed | A Study to Evaluate the Safety and Efficacy of a Nasal Spray to Treat Seasonal Allergies NCT01368445 | Meda Pharmaceuticals | Phase 3 |
| Terminated | Treatment of Olfactory Dysfunction in Seasonal Allergic Rhinitis NCT00361439 | University of Chicago | Phase 4 |
| Completed | Study to Assess the Effect of a Combination of Cetirizine With Pseudoephedrine Versus Cetirizine Alone on Symp NCT00334698 | Fraunhofer-Institute of Toxicology and Experimental Medicine | N/A |
| Completed | Mometasone Furoate on Sleep Disturbances in Subjects With Seasonal Allergic Rhinitis (Study P04608) (COMPLETED NCT00358527 | Organon and Co | Phase 4 |
| Withdrawn | Adolescent and Adult Subjects With Asthma and Seasonal Allergic Rhinitis Receiving Advair Diskus or Placebo NCT00385463 | Creighton University | N/A |
| Completed | A Pilot Monocenter Study to Assess Cellular and Soluble Biomarkers in Nasal Secretions NCT00297843 | Fraunhofer-Institute of Toxicology and Experimental Medicine | — |
| Completed | Trial With Rhinitic Patients Taking GSK256066 Versus Placebo In A Pollen Challenge Chamber NCT00377728 | GlaxoSmithKline | Phase 2 |
| Completed | Safety and Efficacy of Ciclesonide in Pediatric Patients (6 to 11 Years of Age) With Seasonal Allergic Rhiniti NCT00305487 | AstraZeneca | Phase 3 |
| Completed | The Role of Pollen Starch Granules in Pollen Challenge Studies in the Fraunhofer Environmental Exposure Unit NCT00209365 | Fraunhofer-Institute of Toxicology and Experimental Medicine | N/A |
| Completed | Efficacy Study for the Symptomatic Treatment of Seasonal Allergic Rhinitis NCT00504933 | Faes Farma, S.A. | Phase 3 |
| Completed | POPULAR (Preference Of Patient Using Levocetirizine in Allergic Rhinitis) NCT00160537 | UCB Pharma | Phase 4 |
| Completed | Desloratadine With Oxybutynin for the Treatment of Seasonal Allergic Rhinitis and Post-Nasal Drip (Study P0425 NCT00816972 | Organon and Co | Phase 2 |
| Completed | Effects of Orotic Acid Derivatives With or Without Glutathione on Allergic Rhinitis NCT00227058 | University of Mississippi Medical Center | N/A |
| Completed | Study In Adults And Adolescents With Seasonal Allergic Rhinitis NCT00115622 | GlaxoSmithKline | Phase 3 |
| Terminated | Seasonal Allergic Rhinitis and Driving Ability NCT00223587 | Utrecht Institute for Pharmaceutical Sciences | Phase 4 |
| Completed | Efficacy and Safety of Desloratadine vs. Fexofenadine 180 mg. vs. Placebo for Treating Seasonal Allergic Rhini NCT00783211 | Organon and Co | Phase 4 |
| Completed | Efficacy and Safety of Desloratadine vs. Fexofenadine 180 mg. vs. Placebo for Treating Seasonal Allergic Rhini NCT00783146 | Organon and Co | Phase 4 |
| Completed | Single Center, Randomized, Double-Blind,Crossover Study Comparing Effects Of Single-Dose Fexofenadine HCl 180 NCT00637455 | Sanofi | Phase 4 |
| Completed | A Phase III Efficacy Study of the Symptomatic Treatment of Seasonal Allergic Rhinitis With Bilastine NCT01108783 | Faes Farma, S.A. | Phase 3 |
| Completed | Rhinocort Aqua Versus Placebo and Fluticasone Propionate NCT00641680 | AstraZeneca | Phase 3 |
| Completed | Single-Center, Double-Blind, Randomized , Parallel Study Comparing Onset of Action, Efficacy & Safety of a Sin NCT00637611 | Sanofi | Phase 4 |
| Completed | Comparison of Perennial and Preseasonal Subcutaneous Immunotherapy NCT01555736 | Medical University of Lodz | Phase 4 |
| Completed | Preference for Clarinex Tablets vs. Zyrtec Tablets in Patients With Allergies (P03180) NCT00794846 | Organon and Co | Phase 4 |
| Completed | Preference for Clarinex Tablets vs. Zyrtec Tablets in Patients With Allergies (P03181) NCT00794495 | Organon and Co | Phase 4 |
| Completed | Preference for Clarinex Tablets vs. Zyrtec Tablets in Patients With Allergies (P03182) NCT00794599 | Organon and Co | Phase 4 |
| Completed | Preference for Clarinex Tablets vs. Allegra Tablets in Patients With Seasonal Allergies (Study P03177) NCT00783133 | Organon and Co | Phase 4 |
| Completed | Preference for Clarinex Tablets vs Allegra Tablets in Patients With Seasonal Allergies (P03178) NCT00794768 | Organon and Co | Phase 4 |
| Completed | Preference for Clarinex Tablets vs. Allegra Tablets in Patients With Seasonal Allergies (Study P03179) NCT00794248 | Organon and Co | Phase 4 |
| Completed | New Nasal Applicator / New Formulation - User Study NCT00641979 | AstraZeneca | Phase 2 |
| Completed | Comparison of the Effects of Desloratadine and Placebo in the Relief of Nasal Symptom Scores in Subjects With NCT00867191 | Organon and Co | Phase 4 |
| Completed | Montelukast in Seasonal Allergic Rhinitis: Fall 2001 Study (0476-240) NCT00963469 | Organon and Co | Phase 3 |
| Completed | DNA Vaccine for Ragweed Allergic Adults NCT00346086 | Johns Hopkins University | Phase 2 |
| Completed | Montelukast in Seasonal Allergic Rhinitis - Spring 2001 Study (0476-235) NCT00972738 | Organon and Co | Phase 3 |
| Completed | A Study Comparing Montelukast With Placebo in Children With Seasonal Allergic Rhinitis (0476-219)(COMPLETED) NCT00968149 | Organon and Co | Phase 3 |
| Completed | A Study Investigating the Effect of Montelukast in Patients With Seasonal Allergic Rhinitis (MK-0476-192)(COMP NCT00960141 | Organon and Co | Phase 3 |
| Completed | Montelukast in Patients With Seasonal Allergic Rhinitis - Spring 2000 Study (MK-0476A-162)(COMPLETED) NCT00979901 | Organon and Co | Phase 3 |
| Completed | Montelukast in Seasonal Allergic Rhinitis - Fall 1999 Study (0476A-117) NCT00963599 | Organon and Co | Phase 3 |
| Completed | Safety and Efficacy of Mometasone Furoate (SCH 032088) vs Beclomethasone Dipropionate or Placebo in Seasonal A NCT03855189 | Organon and Co | Phase 3 |
| Completed | A Study Comparing the Bioequivalence of Triamcinolone Acetonide Aqueous Nasal Spray (Apotex, Inc.) to That of NCT00987233 | Apotex Inc. | Phase 3 |
| Completed | Effect of Intranasal Corticosteroids on Systemic Allergen Specific IgE NCT00755066 | Medical University of Vienna | N/A |