Allergen-specific immunotherapy (SIT), the administration of gradually increasing quantities of an allergen extract to an allergic patient, is a curative approach which directly treats the underlying allergic disease. Tree MATA MPL has been developed to provide pre-seasonal specific immunotherapy for patients with an allergy to tree pollen (hay fever). The purpose of this double-blind Phase IIb study is to assess the tolerability and immunogenicity of different doses of Tree MATA MPL in volunteers allergic to birch, hazel and alder pollen.

Condition	Intervention	Phase
Type I Hypersensitivity	Vaccine: Tree MATA MPL	Phase II

Further Study Details: 

Primary Outcomes: immunological response to the three Tree MATA MPL treatment arms compared to placebo (birch specific)
Secondary Outcomes: tolerability of different subcutaneous doses; tolerability of the cumulative subcutaneous doses; clinical chemistry and hematology; number of adverse events; number of adverse reactions; immunological response to the three Tree MATA MPL treatment arms compared to placebo (alder and hazel specific)
Expected Total Enrollment:  68

Ages Eligible for Study:  18 Years   -   50 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• Patients must have a positive skin prick test for birch and hazel and alder allergen.
• Positive skin prick test to positive histamine control
• Negative skin prick test to negative control
• Specific IgE for birch as documented by radioallergosorbent or equivalent test with class ≥ 2
• History of at least 1 season of moderate to severe seasonal rhinoconjunctivitis due to an IgE – mediated allergy to pollen from birch, hazel, and alder
• Patients must score on the disease severity questionnaire as moderate or severe.
• Males or non-pregnant, non-lactating females
• Patients who are normally active and otherwise judged to be in good health
• Patients must be willing and able to attend required study visits.
• Patients must be able to follow instructions.
• Patients must be willing and able to give written informed consent and must provide this consent.

Exclusion Criteria:

• Acute or subacute atopic dermatitis and/or urticaria factitia and/or urticaria due to physical or chemical influence and/or chronic dermatitis
• Moderate to severe asthma
• Visual inspection of the forearms indicates potential problems with the conduct or interpretation of the skin prick test; both forearms must be available for testing.
• History or presence of diabetes, cancer or any clinically significant cardiac, metabolic, renal, or hematologic diseases or disorders
• Recent clinically significant history of hepatic, gastrointestinal, dermatologic, venereal, neurologic or psychiatric diseases or disorders
• Any clinically significant abnormal laboratory value at Visit 1
• Perennial allergens: clinically relevant sensitivity to house dust mites, molds, and epithelia
• Patient has clinically relevant sensitivity to the following summer/autumn season flowering plants: plantain, orache, nettle, mugwort, Parietaria judaica, Bermuda grass, or ragweed.
• Secondary alteration at the affected organ
• History of autoimmune diseases and/or rheumatoid diseases
• Patient is taking ß-blockers for any indication including eye drops
• Patient who is not allowed to receive adrenalin
• Patients in whom tyrosine metabolism is disturbed
• Presence of a disease with a pathogenesis interfering with the immune response and patient has received medication which could influence the results of this study
• Acute or significant chronic infection
• History of anaphylaxis
• Documented history of angioedema
• Hypersensitivity to excipients in the study medications
• Previous or current immunotherapy with comparable tree allergen extracts
• Currently using anti-allergy medication and other drugs with antihistaminic activity
• Patients currently participating in a clinical trial or who have been exposed to study medication within the last 30 days
• Patients who cannot communicate reliably with the Investigator or who are not likely to cooperate with the requirements of the study
• Patient is pregnant or planning pregnancy and/or lactating
• Patient has received treatment with preparation containing MPL during the past 12 months
• Concurrent use of any prohibited medication(s), as listed in the study protocol, or inadequate washout of any medication
• Any systemic disorder that could interfere with the evaluation of the study medication(s)
• Clinical history of drug or alcohol abuse, at the Investigator’s discretion, that would interfere with the patient’s participation in the study
• Study site staff or immediate relatives of study site staff or other individuals who would have access to the clinical study protocol

Please refer to this study by ClinicalTrials.gov identifier  NCT00118612

Canada, Ontario
      Allied Research International Inc., Mississauga,  Ontario,  L4W 1N2,  Canada; Recruiting

Study chairs or principal investigators

Deepen Patel, MD,  Principal Investigator,  Allied Research International Inc.   

Study ID Numbers:  TreeMATAMPL203; P2DP05003
Record last reviewed:  July 2005
Last Updated:  July 25, 2005
Record first received:  July 11, 2005
ClinicalTrials.gov Identifier:  NCT00118612
Health Authority: United States: Food and Drug Administration; Canada: Health Canada
ClinicalTrials.gov processed this record on 2005-07-26