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Short-course subcutaneous treatment with PQ Grass strongly improves symptom and medication scores in grass allergy.
- Source :
-
Allergy [Allergy] 2023 Oct; Vol. 78 (10), pp. 2756-2766. Date of Electronic Publication: 2023 Jun 27. - Publication Year :
- 2023
-
Abstract
- Background: A modified grass allergen subcutaneous immunotherapy (SCIT) product with MicroCrystalline Tyrosine and monophosphoryl lipid-A as an adjuvant system (Grass MATA MPL [PQ Grass]) is being developed as short-course treatment of grass-pollen allergic rhinitis (SAR) and/or rhinoconjunctivitis. We sought to evaluate the combined symptom and medication score (CSMS) of the optimized cumulative dose of 27,600 standardized units (SU) PQ Grass in a field setting prior to embarking on a pivotal Phase III trial.<br />Methods: In this exploratory, randomized, double-blind, placebo-controlled trial subjects were enrolled across 14 sites (Germany and the United States of America). Six pre-seasonal subcutaneous injections of PQ Grass (using conventional or extended regimens) or placebo were administered to 119 subjects (aged 18-65 years) with moderate-to-severe SAR with or without asthma that was well-controlled. The primary efficacy endpoint was CSMS during peak grass pollen season (GPS). Secondary endpoints included Rhinoconjunctivitis Quality of Life Questionnaire standardized (RQLQ-S) and allergen-specific IgG4 response.<br />Results: The mean CSMS compared to placebo was 33.1% (p = .0325) and 39.5% (p = .0112) for the conventional and extended regimens, respectively. An increase in IgG4 was shown for both regimens (p < .01) as well as an improvement in total RQLQ-S for the extended regimen (mean change -0.72, p = .02). Both regimens were well-tolerated.<br />Conclusions: This trial demonstrated a clinically relevant and statistically significant efficacy response to PQ Grass. Unprecedented effect sizes were reached for grass allergy of up to ≈40% compared to placebo for CSMS after only six PQ Grass injections. Both PQ Grass regimens were considered equally safe and well-tolerated. Based on enhanced efficacy profile extended regime will be progressed to the pivotal Phase III trial.<br /> (© 2023 Allergy Therapeutics Plc and The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.)
- Subjects :
- Humans
Adult
Male
Female
Middle Aged
Young Adult
Treatment Outcome
Injections, Subcutaneous
Adolescent
Aged
Double-Blind Method
Quality of Life
Poaceae immunology
Rhinitis, Allergic, Seasonal drug therapy
Rhinitis, Allergic, Seasonal therapy
Rhinitis, Allergic, Seasonal diagnosis
Desensitization, Immunologic methods
Allergens administration & dosage
Allergens immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1398-9995
- Volume :
- 78
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Allergy
- Publication Type :
- Academic Journal
- Accession number :
- 37366581
- Full Text :
- https://doi.org/10.1111/all.15788