Centre de Recherche Appliqué en Allergie de Québec
Québec, Quebec, G1V 4M6, Canada
NCT Number: NCT01166061
Grass pollen allergens are universally recognised as a major cause of allergic diseases in humans and animals, including asthma, allergic rhinitis, conjunctivitis and dermatitis. Worldwide, at least 40% of allergic patients are sensitized to grass pollen allergens and between 50-90% of hayfever or seasonal allergy sufferers are allergic to grass pollen.
ToleroMune Grass is a novel, synthetic, allergen-derived peptide desensitising vaccine, currently being developed for the treatment of grass allergy.
The purpose of the present study is to evaluate the safety and tolerability of multiple ascending doses of ToleroMune Grass in subjects allergic to grass.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Québec, Quebec, G1V 4M6, Canada
This study is designed as a randomised, double-blind, placebo-controlled study to evaluate the safety and tolerability of escalating multiple doses of ToleroMune Grass in subjects with a documented history of allergic rhinoconjunctivitis on exposure to grass. The efficacy of ToleroMune HDM will also be explored LPSR, EPSR, CPT and levels of grass specific IgE.
The study will consist of 3 study periods. In Period 1, Screening will be performed up to a maximum of 6 weeks before randomisation.
Period 2 (Treatment Period) will consist of 4 visits (Visits 3A-3D) four weeks apart. The first cohort will receive the lowest dose and successive dose groups will increasing doses of ToleroMune Grass, provided the first administration of the previous dose was safe and well tolerated.
In Period 3, 2 Post-treatment Challenge visits will take place, the first will be 2 weeks after the last administration in the Treatment Period and the second will be 17 weeks after the first administration. Follow-up will be conducted 3-10 days after the second PTC.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Solution resembling active solution but without peptides
1 x4 administrations 4 weeks apart
Time frame: Upto 22 weeks
Time frame: Baseline and 14 weeks
Time frame: Baseline and 14 weeks
Time frame: Baseline and 4 weeks
Time frame: Baseline and 14 weeks
Time frame: Baseline and 14 weeks
Time frame: Baseline and 17 weeks
Time frame: Baseline and 17 weeks
Time frame: Baseline and 17 weeks
Time frame: 17 weeks after start of treatment
Time frame: Baseline and 8 weeks
Time frame: Baseline and 12 weeks
Time frame: Baseline and 14 weeks
Circassia Limited
Industry
An Escalating, Multiple-dose Study in Grass Allergic Subjects to Assess the Safety of Intradermal Injection of ToleroMune Grass
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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