smell
Sponsors
ROXALL Medizin GmbH, ROXALL Medizin GmbH, ROXALL Medizin GmbH, National Defense Medical Center, Taiwan
Conditions
2008)2008) guidelineBousquet et al.Breast MilkInfant BehaviorModerate-to-severe allergic rhinitis / rhino-conjunctivitis due to house dust mites (HDM) for at least one year according to the "Allergic Rhinitis and its Impact on Asthma" (ARIAModerate-to-severe allergic rhinitis / rhinoconjunctivitis due to birch pollen
for at least two years according to the Allergic Rhinitis and its Impact on Asthma (ARIA)
guidelineModerate-to-severe allergic rhinitis / rhinoconjunctivitis due to grass pollen
for at least two years according to the Allergic Rhinitis and its Impact on Asthma (ARIA)
guideline
Phase 2
Phase II-III study to assess the efficacy and safety of
sublingual immunotherapy in patients suffering from birch
pollen allergy
CompletedCTIS2023-505567-37-00
Start: 2023-08-22End: 2024-10-11Target: 30Updated: 2023-08-22
Phase II-III study to assess efficacy and safety of sublingual immunotherapy in patients suffering from grass pollen allergy
CompletedCTIS2023-505880-35-00
Start: 2023-11-10End: 2024-11-07Target: 30Updated: 2023-11-15
Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from Olea europaea pollen allergy
CompletedCTIS2024-511383-88-00
Start: 2024-09-01End: 2025-10-14Target: 50Updated: 2024-07-11
Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from house dust mite allergy
Active, not recruitingCTIS2024-517014-15-00
Start: 2025-05-07Target: 60Updated: 2025-07-16
Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from birch pollen allergy
Active, not recruitingCTIS2024-517515-75-00
Start: 2025-07-17Target: 40Updated: 2025-04-11
Phase II-III study to assess the efficacy and safety of sublingual immunotherapy in patients suffering from birch pollen allergy
Not yet recruitingCTIS2024-517520-19-00
Target: 30Updated: 2025-05-27
Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from grass pollen allergy
Active, not recruitingCTIS2024-517521-25-00
Start: 2025-10-20Target: 30Updated: 2025-08-18