Tolerability of SLIT With LAIS® 2-Tree Allergoid Tablets
NCT02553590 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 160
Last updated 2015-11-11
Summary
To expand knowledge on the application and tolerability of immunotherapy with LAIS® 2-tree allergoid tablets as well as knowledge on the alleviation of symptoms during sublingual therapy in special consideration of the chosen titration schedule in everyday practice.
Conditions
- Allergic Rhinitis
Sponsors & Collaborators
-
University Hospital of Cologne
lead OTHER
Principal Investigators
-
Ralph Mösges, Professor · University Hospital of Cologne
Eligibility
- Min Age
- 5 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-31
- Primary Completion
- 2015-10-31
- Completion
- 2015-10-31
Countries
- Germany
Study Locations
More Related Trials
-
Phase III Study to Assess the Long Term Efficacy, Carry-over Effect and Safety of 300 IR Sublingual Immunotherapy Tablets
NCT00418379 ·Status: COMPLETED ·Phase: PHASE3
-
ILIT: Follow-up of Rhinitis Quality of Life
NCT05037955 ·Status: COMPLETED
-
Effects of Sublingual Immunotherapy on Grasspollen Allergy
NCT00150514 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Efficacy and Safety of 300 IR Sublingual Immunotherapy (SLIT) Tablets in Adult Patients With Allergic Grass Pollen Rhinoconjunctivitis
NCT00955825 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy on Phase III Study on 300 IR SLIT to Patients Suffering From Grass Pollen Rhinoconjunctivitis
NCT00803244 ·Status: COMPLETED ·Phase: PHASE3
-
Safety, Tolerability and Pharmacodynamic Effects of Sublingual Immunotherapy (Tablets) With Recombinant Bet v1
NCT00396149 ·Status: COMPLETED ·Phase: PHASE1
-
App Based Study on the Symptoms of Patients With Allergic Rhinitis in the Pollen Season
NCT03112252 ·Status: COMPLETED
-
Perennial Allergic Rhinitis In Pediatric Subjects
NCT00257595 ·Status: COMPLETED ·Phase: PHASE3
-
Non-interventional Study to Assess the Tolerability, the Safety Profile and the Adherence of Different Up-dosing Schemes for a Sublingual Immunotherapy Treatment
NCT03097432 ·Status: COMPLETED
-
Clinical Trial to Evaluate the Safety and Efficacy of "CITUS Dry Syrup" in Children With Perennial Allergic Rhinitis
NCT01539304 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy Study of Sublingual Immunotherapy to Treat Ragweed Allergies
NCT00599872 ·Status: COMPLETED ·Phase: PHASE3
-
Local IgE in Subjects With Allergic or Non-allergic Rhinitis
NCT02810535 ·Status: COMPLETED ·Phase: NA
-
Implementation of an Allergic Rhinitis Severity Questionnaire in ENT Consultations
NCT07315945 ·Status: RECRUITING
-
A Study in Children and Adolescents With Birch Pollen-induced Rhinoconjunctivitis
NCT04878354 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Effectiveness and Safety of Sublingual Immunotherapy in Children With Allergic Rhinitis
NCT00698594 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Tolerability of Two Different Administration Routes With SLITonePLUS Birch
NCT01191359 ·Status: COMPLETED ·Phase: PHASE2
-
The Role of the Nasal Allergen Provocation Test in Starting and Monitoring Allergen Immunotherapy
NCT04544774 ·Status: RECRUITING
-
Efficacy and Safety of Specific Immunotherapy With CLUSTOID Grass Pollen
NCT01012531 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Tolerability Study of Ragweed SLIT Tablets
NCT01224834 ·Status: COMPLETED ·Phase: PHASE1
-
Quality of Life in Patients With Allergic Rhinitis: Clinical Trial With Bilastine or Loratadine
NCT02513290 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy of Sublingual Immunotherapy (SLIT) Tablets in Grass Pollen Rhinoconjunctivitis
NCT00367640 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Effect of Sublingual Immunotherapy on Platlet factor4 Level in Children
NCT04851860 ·Status: UNKNOWN ·Phase: PHASE3
-
Efficacy and Safety Trial of SLITone(TM) Birch in Subjects With Hayfever
NCT00310466 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluation of Safety of Levocetirizine in Routine Clinical Practice-non- Interventional Study
NCT00598780 ·Status: COMPLETED
-
Evaluation of Treatment Satisfaction in Children With an Allergy and Who Received an Antihistamine
NCT00453583 ·Status: COMPLETED