Annual Congress 2023 of the European Academy of Allergy and Clinical Immunology: New Adaptive Trial Design Supports Evaluation of Therapeutic Strategies for Allergic Patients

In a recent Phase II study, PQ Grass demonstrated a significant dose-response relationship in reducing symptoms, leading to the identification of the optimally effective and safe cumulative dose of 27,600 standardised units (SU). Building on these promising results, an exploratory Phase III trial was conducted to evaluate the combined symptom and medication score (CSMS) of PQ Grass compared to placebo. In a recent Phase II study, PQ Grass demonstrated a significant dose-response relationship in...
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In a recent Phase II study, PQ Grass demonstrated a significant dose-response relationship in reducing symptoms, leading to the identification of the optimally effective and safe cumulative dose of 27,600 standardised units (SU). Building on these promising results, an exploratory Phase III trial was conducted to evaluate the combined symptom and medication score (CSMS) of PQ Grass compared to placebo.

The trial employed a randomized, parallel-group, double-blind, placebo-controlled design across 14 sites in the United States and Germany. Subjects were randomized into four treatment groups, including two PQ Grass groups receiving either a conventional or extended regimen, and two placebo groups receiving an active placebo or saline. The primary efficacy endpoint was the CSMS averaged over the peak grass pollen season (GPS).

The results of the trial demonstrated a significant improvement in the CSMS for both the PQ Grass extended and conventional regimens compared to placebo, with relative reductions of 39.5% and 33.1%, respectively. This translates to an absolute reduction in symptoms of 0.67 and 0.56 points compared to placebo. The PQ Grass extended regimen also showed a significant improvement in the total combined score (TCS).

"These findings highlight the potential of PQ Grass as an effective therapeutic option for allergic patients. The adaptive trial design utilized in this study enables a more efficient evaluation of treatment strategies, providing valuable insights into the clinical and immunological effects of novel therapies. The results support the continued development of PQ Grass and its potential to address the unmet needs of allergic patients by offering a short-course SCIT treatment option," says EAACI VP Congresses, Professor of Immunology and Allergy of Imperial College London Mohamed Shamji.

Annual Congress 2023 of the European Academy of Allergy and Clinical Immunology: New Adaptive Trial Design Supports Evaluation of Therapeutic Strategies for Allergic Patients

Further research and clinical studies will be conducted to confirm the safety and efficacy of PQ Grass. If approved, this innovative therapeutic approach could significantly impact the management of allergic rhinitis and rhinoconjunctivitis, offering a potential cure for patients suffering from these chronic allergic conditions.

About EAACI:
The European Academy of Allergy and Clinical Immunology (EAACI) is an association of clinicians,researchers and allied health professionals founded in 1956. EAACI is dedicated to improving the healthof people affected by allergic diseases. With more 13 000 members from 125 countries and over 75National Allergy Societies, EAACI is the primary source of expertise in Europe and worldwide for allaspects of allergy. 

Contact: 
EAACI Headquarters, Hagenholzstrasse 111, 3rd Floor 8050 Zurich, CH- Switzerland 
Tel: +41799561865 
communications@eaaci.org 
www.eaaci.org

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