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2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test
BACKGROUND: Clinical efficacy of a depigmented polymerized birch pollen extract has been shown in 2 large phase III studies with 1000 DPP/mL. To date dose-response studies are required to show optimal efficacy at a defined allergen dose. The conjunctival provocation test (CPT) is a possible outcome...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Allergy Organization Journal
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3513073/ http://dx.doi.org/10.1097/01.WOX.0000411747.36918.e1 |
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author | Sager, Angelika Worm, Margitta |
author_facet | Sager, Angelika Worm, Margitta |
author_sort | Sager, Angelika |
collection | PubMed |
description | BACKGROUND: Clinical efficacy of a depigmented polymerized birch pollen extract has been shown in 2 large phase III studies with 1000 DPP/mL. To date dose-response studies are required to show optimal efficacy at a defined allergen dose. The conjunctival provocation test (CPT) is a possible outcome parameter and from the regulatory authorities accepted test procedure. METHODS: 301 (PP) patients with confirmed rhinitis and/or rhinoconjunctivitis were treated in a double-blind study with 4 doses of 100 DPP/mL, 1000 DPP/mL, 5000 DPP/mL and 10.000 DPP/mL allergen extract over 22 weeks in Germany, Poland, and Lithuania. A 1-day build-up phase applying 0.1 mL and 2 times 0.2 mL allergen extract was followed by a maintenance period applying 0.5 mL in 3 to 4 weeks intervals. Before treatment a CPT was performed with semi-logarithmically increasing doses up to 10,000 SQ-U/mL of native birch extract, after treatment the CPT was repeated with doses up to 100,000 SQ-U/mL. The main parameter was the percentage of patients with an increase of allergen extract to provoke a positive CPT after SIT. Secondary parameters were specific IgE, IgG1 and IgG4 as well as safety. The main parameter was investigated using a hierarchic test procedure comparing the highest dose against the lowest, if statistically significant testing the next lower dose against the lowest until the difference was no longer significant. RESULTS: An increase in allergen amount to provoke a positive CPT after SIT was reached in 37.5% of the 100 DPP/mL, 50.7% of the 1000 DPP/mL, 54.9% of the 5000 DPP/mL and 55.8% of the 10,000 DPP/mL group. Results compared to the lowest dose were statistically significant for the 5000 DPP/mL (P = 0.0236) and 10,000 DPP/mL group (P = 0.0159). Specific IgEs remained stable in all groups whereas specific IgG1 and IgG4 showed dose-dependent increases. Grade 1 systemic reactions occurred in 18% (100 DPP/mL), 14.8% (1000 DPP/mL), 17.4% (5000 DPP/mL) and 25.3% (10,000 DPP/mL) of patients. CONCLUSIONS: We determined increased allergen amounts to obtain a positive CPT after SIT from 1000 to 10,000 DPP/mL depigmented polymerized birch pollen extract. The 5000 DPP/mL dose extract suggest a good benefit/risk ratio with the potential for further development. |
format | Online Article Text |
id | pubmed-3513073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | World Allergy Organization Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-35130732012-12-21 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test Sager, Angelika Worm, Margitta World Allergy Organ J Abstracts of the XXII World Allergy Congress BACKGROUND: Clinical efficacy of a depigmented polymerized birch pollen extract has been shown in 2 large phase III studies with 1000 DPP/mL. To date dose-response studies are required to show optimal efficacy at a defined allergen dose. The conjunctival provocation test (CPT) is a possible outcome parameter and from the regulatory authorities accepted test procedure. METHODS: 301 (PP) patients with confirmed rhinitis and/or rhinoconjunctivitis were treated in a double-blind study with 4 doses of 100 DPP/mL, 1000 DPP/mL, 5000 DPP/mL and 10.000 DPP/mL allergen extract over 22 weeks in Germany, Poland, and Lithuania. A 1-day build-up phase applying 0.1 mL and 2 times 0.2 mL allergen extract was followed by a maintenance period applying 0.5 mL in 3 to 4 weeks intervals. Before treatment a CPT was performed with semi-logarithmically increasing doses up to 10,000 SQ-U/mL of native birch extract, after treatment the CPT was repeated with doses up to 100,000 SQ-U/mL. The main parameter was the percentage of patients with an increase of allergen extract to provoke a positive CPT after SIT. Secondary parameters were specific IgE, IgG1 and IgG4 as well as safety. The main parameter was investigated using a hierarchic test procedure comparing the highest dose against the lowest, if statistically significant testing the next lower dose against the lowest until the difference was no longer significant. RESULTS: An increase in allergen amount to provoke a positive CPT after SIT was reached in 37.5% of the 100 DPP/mL, 50.7% of the 1000 DPP/mL, 54.9% of the 5000 DPP/mL and 55.8% of the 10,000 DPP/mL group. Results compared to the lowest dose were statistically significant for the 5000 DPP/mL (P = 0.0236) and 10,000 DPP/mL group (P = 0.0159). Specific IgEs remained stable in all groups whereas specific IgG1 and IgG4 showed dose-dependent increases. Grade 1 systemic reactions occurred in 18% (100 DPP/mL), 14.8% (1000 DPP/mL), 17.4% (5000 DPP/mL) and 25.3% (10,000 DPP/mL) of patients. CONCLUSIONS: We determined increased allergen amounts to obtain a positive CPT after SIT from 1000 to 10,000 DPP/mL depigmented polymerized birch pollen extract. The 5000 DPP/mL dose extract suggest a good benefit/risk ratio with the potential for further development. World Allergy Organization Journal 2012-02-17 /pmc/articles/PMC3513073/ http://dx.doi.org/10.1097/01.WOX.0000411747.36918.e1 Text en Copyright © 2012 by World Allergy Organization |
spellingShingle | Abstracts of the XXII World Allergy Congress Sager, Angelika Worm, Margitta 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title | 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title_full | 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title_fullStr | 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title_full_unstemmed | 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title_short | 2 Dose Optimizing Study of a Depigmented Polymerized Allergen Extract of Birch Pollen by Means of Conjunctival Provocation Test |
title_sort | 2 dose optimizing study of a depigmented polymerized allergen extract of birch pollen by means of conjunctival provocation test |
topic | Abstracts of the XXII World Allergy Congress |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3513073/ http://dx.doi.org/10.1097/01.WOX.0000411747.36918.e1 |
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