| Eligibility |
Inclusion Criteria:
- Patients must be male or female and aged 18 to 50 years inclusive.
- Patients must have at least a two-year clinical history of SAR due to birch pollen
allergy.
- Patients must have allergy to tree pollen allergen, defined by positive case history
and positive skin prick test for tree pollen allergen (wheals of = 5 mm (birch) and =
3 mm (hazel and alder) greater than the negative control after skin prick testing) at
Visit 1. Patients who will be skin tested at Visit 1 must adhere to the washout time
for antihistamines.
- Specific IgE for birch tree pollen as documented by a radioallergosorbent test (RAST),
or equivalent test, with class = 2.
- Patients must obtain minimum qualifying symptom scores on the final two pre-treatment
birch pollen exposure sessions (Visits 4 and 5) to be enrolled into the study. Minimum
qualifying symptom scores are defined as a TSS of at least 12 out of a possible 24 and
a NSS of at least 7 out of a possible 12 on at least one symptom diary card on each of
Visits 4 and 5. Furthermore, a minimum priming criteria for NSS of 7 out of a possible
12, including a score of at least 2 for runny nose, on two diary cards during each of
Visits 4 and 5, must be obtained.
- Patients must observe the drug washout times prior to Screening (Visit 1). The use of
other medications will be permitted if they are not expected to interfere with the
ability of the patient to participate in the study and provided they have been on a
stable regimen (i.e., the same dosage and administration) for six weeks prior to
Screening.
- Males or non-pregnant, non-lactating females who are post-menopausal or naturally or
surgically sterile (hysterectomy; bilateral oophorectomy; bilateral tubal ligation
with surgery at least 6 weeks prior to study initiation). Postmenopausal is defined as
at least 12 months natural spontaneous amenorrhea, or at least six weeks following
surgical menopause (bilateral oophorectomy). Females of childbearing potential should
be using one of the following acceptable birth control methods:Intrauterine device
(IUD) in place for at least 3 months;Barrier method (condom or diaphragm) with
spermicide; Stable hormonal contraceptive for at least 3 months prior to study and
through study completion;Abstinence; Non-heterosexual lifestyle.
- Patients who are normally active and otherwise judged to be in good health on the
basis of medical history, physical examination and routine laboratory tests.
- Patients must be willing and able to give written informed consent and must provide
this consent.
- Patients must be willing and able to attend required study visits. 11.Patients must be
able to follow instructions.
Exclusion Criteria:
A patient will not be included in this study if one or more of the following criteria
apply:
- Have a positive skin prick test [wheal (longest diameter) = 3 mm greater than the
negative control] at Visit 1 to any of the following perennial allergens: house dust
mites (Dermatophagoides pteronyssinus and Dermatophagoides farinae), molds
(Cladosporium cladosporioides, Alternaria alternata, Penicillium chyrsogenum
(notatum), and Aspergillus fumigatus), or epithelia (cat, dog, and horse). In these
cases, a careful history is to be taken and if moderate or severe symptoms are
reported when exposed to the aforementioned allergens, the subject is to be excluded.
Exception: the source of the allergen (cat, dog, horse) can be avoided for the entire
study. Subjects with mild or no symptoms when exposed to the aforementioned allergens
during the 3 years prior to Visit 1 will be allowed to enroll. Mild symptoms are
defined as: sign/symptom clearly present, but minimal awareness, easily tolerated.
- Concurrent disease that might complicate or interfere with investigation or evaluation
of the study medications or the skin prick test result, such as:
Rhinitis medicamentosa; Large obstructive nasal polyps; Documented evidence of acute or
significant chronic sinusitis, or upper respiratory tract infection as determined by the
individual Investigator; Asthma, with the exception of mild intermittent asthma, to lessen
confounding by asthma medications; History of hospitalization for asthma; History or
presence of acute or subacute atopic dermatitis, chronic dermatitis, urticaria factitia, or
urticaria due to physical/chemical influence.
- Current diagnosis of seasonal asthma caused by tree pollen exposure.
- Concurrent use or inadequate washout of any prohibited medication.
- Chronic or intermittent use of inhaled, nasal, ocular, oral, intramuscular,
intravenous, or potent or super-potent topical corticosteroids (as assessed by the
Investigator).
- Chronic use of long acting antihistamines and other concomitant medications (e.g.,
tricyclic antidepressants) that would affect assessment of the effectiveness of study
drug(s).
- Are pregnant or lactating.
- Any systemic disorder that could interfere with the evaluation of the study
medication(s).
- Upper or lower respiratory infection requiring antibiotics within 14 days of Visit 2.
- Diagnosis of sinusitis within 30 days of Visit 2.
- Any ocular disorder (other than allergic conjunctivitis) including presumed infectious
ocular disease (bacterial, fungal, viral, etc.), which could interfere with the
evaluation of the study medication.
- Hypersensitivity to the study drug(s) excipients.
- Patients with active or quiescent tuberculous infection of the respiratory tract,
untreated local or systemic fungal or bacterial or systemic viral infections or
parasitic or ocular herpes simplex.
- Patients who have experienced nasal septal ulcers, nasal surgery or nasal trauma
within 90 days of enrollment into this study.
- Clinical history of anaphylaxis or idiopathic anaphylaxis.
- Patients with a clinical history of immunodeficiency, including those who are on
immunosuppressant therapy.
- Patients with an auto-immune disease (e.g. of liver, kidney, thyroid, nervous system)
- Patients with a history of angioedema
- Patients in whom tyrosine metabolism is disturbed, especially in the case of
tyrosinemia and alkaptonuria.
- Patients with contraindications to adrenaline.
- Patients taking ß-blockers, including eye drops, for any indication.
- Patients taking Monoamine Oxidase Inhibitors
- Current diagnosis of chickenpox or measles.
- Clinical history of drug or alcohol abuse which would, at the Investigator's
discretion, interfere with the patient's participation in the study.
- Clinical history of severe or uncontrolled cardiovascular, pulmonary, hepatic, renal
and/or other disease/illness that could be expected to interfere with the study.
- Clinical history, or evidence, of nasolacrimal drainage system malfunction.
- Study site staff or immediate relatives of study site staff or other individuals who
would have access to the clinical study protocol.
- Patient that has received TreeMATAMPL in any previous clinical trial.
- History of immunotherapy with tree pollen extract, except if treatment was
successfully completed 3 years prior to Visit 1 and SAR symptoms had reappeared prior
to Visit 1.
- Patient received treatment with preparation containing MPL during the past 12 months.
- Participation in any other investigational study within 30 days before Visit 1 or
concomitantly with this study.
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