Grass pollen allergens are recognised as a major cause of allergic diseases in humans and animals. Worldwide, at least 40% of allergic patients are sensitised 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 this optional observational follow-on study is to further evaluate rhinoconjunctivitis symptoms on exposure to Grass in the EEU among subjects who completed all dosing visits in study TG002 approximately one year after the start of treatment.
Subjects who completed all dosing visits and the post treatment challenge (PTC) in study TG002 will be invited to attend the Screening Visit for TG002a. Subjects will attend for 4 visits to the EEU on successive days. Following the last EEC visit a follow-up visit will be performed 3-10 days later.
Study Type
OBSERVATIONAL
Enrollment
163
Total Rhinoconjunctivitis Symptom Score
Time frame: Eighteen months post first dose in TG002
Symptom scores for nasal and non nasal symptoms
Time frame: Eighteen months post first dose in TG002
Skin prick wheal diameter
Time frame: Eighteen months post first dose in TG002
Peak Nasal Inspiratory Flow
Time frame: Eighteen months post first dose in TG002
Grass specific IgA
Time frame: Eighteen months post first dose in TG002
Grass specific IgE
Time frame: Eighteen months post first dose in TG002
Grass specific IgG4
Time frame: Eighteen months post first dose in TG002
Adverse Events
Time frame: Eighteen months post first dose in TG002
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