Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing
Background: Pollinex Quattro Grass (PQ Grass) is an effective, well-tolerated, short pre-seasonal subcutaneous immunotherapy to treat seasonal allergic rhinoconjunctivitis (SAR) due to grass pollen. In this Phase II study, 4 cumulative doses of PQ Grass and placebo were evaluated to determine its op...
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doaj-03d9e3b4b9304063ab7fa1346e39ca332020-11-25T01:16:34ZengElsevierWorld Allergy Organization Journal1939-45512019-11-011211Strong dose response after immunotherapy with PQ grass using conjunctival provocation testingS. Zielen0P. Kuna1W. Aberer2S. Lassmann3O. Pfaar4L. Klimek5A. Wade6K. Kluehr7J. Raab8D. Wessiepe9D. Lee10M.F. Kramer11K. Gunawardena12T. Higenbottam13M.D. Heath14M.A. Skinner15P.J. de Kam16Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic fibrosis, Goethe University, Frankfurt, GermanyPoradnia Alergologii i Chorób Płuc Lodz, PolandDepartment of Dermatology, Medical University of Graz, Graz, AustriaSpecialist in Otolaryngology, Saalfeld, GermanyDepartment of Otorhinolaryngology, Head and Neck Surgery, Section of Rhinology and Allergy, University Hospital Marburg, Philipps-Universität Marburg, GermanyCentre for Rhinology and Allergology, Wiesbaden, GermanyAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKMetronomia Clinical Research GmbH, Munich, GermanyAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UKAllergy Therapeutics Ltd., Worthing, UK; Corresponding author. Allergy Therapeutics (UK) Ltd, Dominion Way Worthing, West Sussex BN14 8SA, UKBackground: Pollinex Quattro Grass (PQ Grass) is an effective, well-tolerated, short pre-seasonal subcutaneous immunotherapy to treat seasonal allergic rhinoconjunctivitis (SAR) due to grass pollen. In this Phase II study, 4 cumulative doses of PQ Grass and placebo were evaluated to determine its optimal cumulative dose. Methods: Patients with grass pollen-induced SAR were randomised to either a cumulative dose of PQ Grass (5100, 14400, 27600 and 35600 SU) or placebo, administered as 6 weekly subcutaneous injections over 31–41 days (EudraCT number 2017-000333-31). Standardized conjunctival provocation tests (CPT) using grass pollen allergen extract were performed at screening, baseline and post-treatment to determine the total symptom score (TSS) assessed approximately 4 weeks after dosing. Three models were pre-defined (Emax, logistic, and linear in log-dose model) to evaluate a dose response relationship. Results: In total, 95.5% of the 447 randomized patients received all 6 injections. A highly statistically significant (p < 0.0001), monotonic dose response was observed for all three pre-specified models. All treatment groups showed a statistically significant decrease from baseline in TSS compared to placebo, with the largest decrease observed after 27600 SU (p < 0.0001). The full course of 6 injections was completed by 95.5% of patients. Treatment-emergent adverse events were similar across PQ Grass groups, and mostly mild and transient in nature. Conclusions: PQ Grass demonstrated a strong curvilinear dose response in TSS following CPT without compromising its safety profile. Keywords: Allergen immunotherapy, Allergoid, Cumulative dose, Curvilinear dose response, Grass pollenhttp://www.sciencedirect.com/science/article/pii/S1939455119312311 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Zielen P. Kuna W. Aberer S. Lassmann O. Pfaar L. Klimek A. Wade K. Kluehr J. Raab D. Wessiepe D. Lee M.F. Kramer K. Gunawardena T. Higenbottam M.D. Heath M.A. Skinner P.J. de Kam |
spellingShingle |
S. Zielen P. Kuna W. Aberer S. Lassmann O. Pfaar L. Klimek A. Wade K. Kluehr J. Raab D. Wessiepe D. Lee M.F. Kramer K. Gunawardena T. Higenbottam M.D. Heath M.A. Skinner P.J. de Kam Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing World Allergy Organization Journal |
author_facet |
S. Zielen P. Kuna W. Aberer S. Lassmann O. Pfaar L. Klimek A. Wade K. Kluehr J. Raab D. Wessiepe D. Lee M.F. Kramer K. Gunawardena T. Higenbottam M.D. Heath M.A. Skinner P.J. de Kam |
author_sort |
S. Zielen |
title |
Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing |
title_short |
Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing |
title_full |
Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing |
title_fullStr |
Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing |
title_full_unstemmed |
Strong dose response after immunotherapy with PQ grass using conjunctival provocation testing |
title_sort |
strong dose response after immunotherapy with pq grass using conjunctival provocation testing |
publisher |
Elsevier |
series |
World Allergy Organization Journal |
issn |
1939-4551 |
publishDate |
2019-11-01 |
description |
Background: Pollinex Quattro Grass (PQ Grass) is an effective, well-tolerated, short pre-seasonal subcutaneous immunotherapy to treat seasonal allergic rhinoconjunctivitis (SAR) due to grass pollen. In this Phase II study, 4 cumulative doses of PQ Grass and placebo were evaluated to determine its optimal cumulative dose. Methods: Patients with grass pollen-induced SAR were randomised to either a cumulative dose of PQ Grass (5100, 14400, 27600 and 35600 SU) or placebo, administered as 6 weekly subcutaneous injections over 31–41 days (EudraCT number 2017-000333-31). Standardized conjunctival provocation tests (CPT) using grass pollen allergen extract were performed at screening, baseline and post-treatment to determine the total symptom score (TSS) assessed approximately 4 weeks after dosing. Three models were pre-defined (Emax, logistic, and linear in log-dose model) to evaluate a dose response relationship. Results: In total, 95.5% of the 447 randomized patients received all 6 injections. A highly statistically significant (p < 0.0001), monotonic dose response was observed for all three pre-specified models. All treatment groups showed a statistically significant decrease from baseline in TSS compared to placebo, with the largest decrease observed after 27600 SU (p < 0.0001). The full course of 6 injections was completed by 95.5% of patients. Treatment-emergent adverse events were similar across PQ Grass groups, and mostly mild and transient in nature. Conclusions: PQ Grass demonstrated a strong curvilinear dose response in TSS following CPT without compromising its safety profile. Keywords: Allergen immunotherapy, Allergoid, Cumulative dose, Curvilinear dose response, Grass pollen |
url |
http://www.sciencedirect.com/science/article/pii/S1939455119312311 |
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