A Study of Tolerability and Safety of a New Cumulative Dose of Grass MATA MPL (G104)

This is an interventional treatment trial for Seasonal Allergic Rhinitis focused on measuring Grass MATA MPL, Safety Read More

Inclusion Criteria:

• Patients must have a positive skin prick test for grass pollen allergen.
• Positive skin prick test to positive histamine control
• Negative skin prick test to negative control
• Specific IgE for grass pollen as documented by ImmunoCAP test with class ≥ 2
• A history of moderate to severe symptoms of seasonal allergic rhinitis and/or conjunctivitis due to grass (Pooideae) pollen exposure that required repeated use of antihistamines, nasal steroids, and/or leukotriene modifiers for relief of symptoms during the last two consecutive seasons prior to the study
• Males or non-pregnant, non-lactating females who are not of child-bearing potential or using effective contraception
• Patients who are normally active and otherwise judged to be in good health
• For patients with a history of asthma, forced expiratory volume in 1 second (FEV1) ≥ 80% of National Health and Nutrition Examination Surveys (NHANES) predicted, with a FEV1/forced vital capacity (FVC) ratio ≥ 70%.
• Able to observe the drug washout times listed in the Prohibited Medications Table below prior to screening
• Patients willing and able to attend required study visits and able to follow the protocol requirements.
• Patients willing and able to give written informed consent.

Exclusion Criteria:

• Symptoms outside the grass pollen season due to a perennial and/or non-grass seasonal allergen, if the patient is unable to avoid the offending allergen.
• Immunological disorders or other diseases that in the opinion of the investigator may pose a safety risk.
• Presence of moderate to severe asthma, characterized by the current use of inhaled steroids at a daily dose above 400 micrograms of budesonide (or equivalent)
• Emergency room visit or admission for asthma in the 12 months prior to Visit 1 or history of a life-threatening asthma attack ever.
• Presence of non-atopic rhinitis and/or rhino-sinusitis (with or without polyps).
• Presence of any skin conditions (skin abnormalities, tattoos etc.) which might interfere with the interpretation of the SPT results.
• Current diagnosis of type I diabetes. Patients with type II diabetes will only be allowed to participate at the discretion of the investigator.
• Treatment with a preparation containing MPL (e.g. Cervarix) within 6 months prior to screening
• Moderate to severe upper or lower respiratory tract infections requiring medication within 14 days of or a diagnosis of sinusitis within 30 days of randomisation
• Clinical history of severe or life-threatening anaphylactic reactions to foods, insect venom, exercise, drugs or idiopathic anaphylaxis.
• Clinical history of allergy, hypersensitivity or intolerance to the excipients of the study medication.
• Tyrosine metabolism disorders, especially tyrosinemia and alkaptonuria.
• Unable to receive epinephrine therapy (i.e., use of epinephrine is contraindicated).
• Clinical history of immunodeficiency, including those who are on immunosuppressant therapy.
• Clinical history of recurrent idiopathic angioedema.
• Beta-blocker medication, including eye drops, for any indication.
• Treatment with monoamine oxidase inhibitors, tricyclic antidepressants or ACE inhibitors.
• Clinical history of drug or alcohol abuse which, in the investigator's opinion, could interfere with the patient's ability to participate in the study.
• Participation in a clinical research trial with any investigational medicinal product within 4 weeks of screening or concomitantly with this study.