A Randomized, Double-blind, Placebo-controlled Study on the Efficacy and Safety of CVT-E002 in the Treatment of Upper Respiratory Tract Infections in a Pediatric (3-11 Years) Population

Afexa Life Sciences Inc293 enrolled

Overview

Parents with children aged 3-11 will participate in this study. About 500 children will take part in the study. We expect about half of those children will develop symptoms of a respiratory infection. Active participation in this study will last 14 days after a parent reports symptoms of a respiratory infection in a participant. Those children who do meet the study criteria of symptoms will then be randomly placed (like a flip of a coin) into one of 2 groups to take either COLD-FX® or placebo for 3 days. A placebo will look exactly like COLD-FX® but contains no active ingredients. The participant has an equal chance of being placed in either of the above groups. The study is double-blind, so neither the participant nor the study staff will know which study group the participant was placed in until the study is completed. If this information is needed in an emergency at any time throughout the study, it is quickly available from the sponsor. Participation in the study will be for 14 days after symptoms of a respiratory infection are reported to study staff. Your child will take the study product for 3 days, you will complete a daily diary, receive 4 phone calls and be seen for a final study visit to review the diary and complete a final health check of your child.

The primary objective is to assess the efficacy of acute dosing of CVT-E002 in reducing the duration of URTI symptoms in children 3-11 years of age. The secondary objectives are to asses the efficacy of acute dosing of CVT-E002 in reducing: (1) symptom severity; (2) peak CARIFS scores and; (3) absenteeism for participant and/or parent/guardian. The ease of administration and the safety of acute dosing of CVT-E002 in children 3-11 years of age will also be assessed.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

293

Eligibility

Sex: ALLMin age: 3 YearsMax age: 11 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Healthy individuals of both genders aged years 3 - 11 2. Willing to adhere to the requirements of the protocol, including availability for follow-up visits 3. Parent/guardian willing and able to sign written consent Exclusion Criteria: 1. Medical conditions: * Asthma requiring treatment in the last 3 months with oral steroids - prednisone greater than 10 mg/day * Received influenza vaccination for the winter season when the trial is run. * Active tuberculosis * Cystic fibrosis * Significant pulmonary disorders (chronic bronchitis, emphysema or other chronic respiratory illness) * Any ongoing allergen immunotherapy during study or for 6 months prior HIV/AIDS * Malignancy (under active observation or treatment) * Unstable cardiovascular disease (physician visit or hospitalization for unstable cardiovascular disease in the last 6 months) * Known renal abnormalities (serum creatinine known to be \> upper limit for age group) * Acute or active chronic liver disease * Diabetes * Neurological or psychiatric disease (progressive or currently under treatment) * Bleeding disorders * Major surgery in the last 6 months or planned surgery over the course of the study * Crohn's disease, Juvenile arthritis, Ulcerative Colitis or any other autoimmune disease * Other serious medical conditions 2. Medications: * Medications for allergic rhinitis/conjunctivitis, including: antihistamines; oral, parenteral, nasal, and ophthalmic corticosteroids; cromolyn sodium; nedocromil; and intranasal anticholinergics (If the participants agree to stop taking these products prior to study entry and for the duration of the study, they can participate in the study.) * Oral or long-acting beta-agonists, theophylline, and leukotriene modifiers * Phenelzine * Pentobarbital * Haloperidol * Warfarin * Heparin * Immunosuppressants * Any other natural health products or dietary supplements, with the exception of vitamins and minerals with dose of \<600 mg/day of vitamin E and containing no vitamin K. Natural health products or dietary supplements include products such as, but not limited to, Echinacea, Ginseng (beverages, foods, extracts, capsules, or tablets), St. John's Wort, Gingko, Glucosamine, Fish Oil supplements, Evening Primrose Oil, Green Tea or other herbal products consumed in the form of a pill or capsule. (If the participants agree to stop taking these products prior to study entry and for the duration of the study, they can participate in the study.) 3. Known allergy to any ingredient in the study product or placebo, including: ginseng, icing sugar, stevia leaf powder, mixed berries natural flavour (MC010946), grape natural flavour (MC010947) or caramel color liquid (DN700 caramelan 8-110).

Locations (4)

Alberta Health Services

Edmonton, Alberta, Canada

Saint John Regional Hospital

Saint John, New Brunswick, Canada

Canadian Center for Vaccinology, Dalhousie University

Halifax, Nova Scotia, Canada

JDM Research

Toronto, Ontario, Canada

Outcomes

Primary Outcomes

The primary objective is to assess the efficacy of acute dosing of CVT-E002 in reducing the duration of URTI symptoms in children 3-11 years of age

Time frame: 14 days

Secondary Outcomes

To asses the efficacy of acute dosing of CVT-E002 in reducing: (1) symptom severity; (2) peak CARIFS scores and; (3) absenteeism for participant and/or parent/guardian.