Seasonal Allergic Rhinitis
Conditions
Keywords
Seasonal allergies, Allergic rhinitis
Brief summary
A single and multiple dose study to assess the safety of JNJ 38224342 compared to placebo in healthy volunteers and in volunteers with seasonal allergies.
Detailed description
A four-part, single and multiple dose study to investigate the safety of JNJ-38224342 versus placebo in healthy patients and in patients with seasonal allergies. Volunteers (or patients) are randomly assigned to one of four treatment groups or Parts. Part 1 and 2 are randomized (study drug will be assigned by chance) and double-blind (neither the physician nor volunteer knows the identity of the assigned drug). In Part 1 patients receive a single oral dose of either 25, 100, 300, 600, 1250 or 2000 mg of JNJ-38224342 or placebo. In Part 2 patients receive multiple oral doses of either 100, 250, 500 or 700 mg of JNJ-38224342 or placebo administered over 14 days. Part 3 (for male volunteers only) is open-label (all people involved know the identity of the assigned drug), 2-period crossover (meaning that volunteers will receive both treatments at different times) study of the effects of food on JNJ-38224342. Participants will be given a single 100 mg oral dose (either solution or capsule formulation). Part 4 is for patients with seasonal allergies only. The dose of JNJ-38224342 will be determined based on information collected in Parts 1 - 3. Patients that participate in part 4 of the study will also have their nasal passage flushed out with salt water and the contents will be collected. Patients will be asked to remain in the clinic for either 5 days or 18 days depending on what part of the study they are participating in. A physical exam will be performed and a medical history collected. Safety evaluations include adverse event monitoring, blood pressure measurements, ECG and lab work requiring blood and urine samples at various time points throughout the study. Single oral dose of either 25, 100, 300, 600, 1250 or 2000mg of JNJ-38224342 or placebo; Multiple oral dose of either 100, 250, 500 or 700 mg of JNJ-38224342 or placebo administered over 14 days; single oral 100mg dose of JNJ 38224342 as a solution versus capsule with or without food; multiple oral doses of JNJ38224342 or placebo administered for up to 14 days where the number of days dosed, actual dose levels, food requirements will be determined based on the data from Parts 1, 2, and 3
Interventions
DRUGJNJ38224342
multiple ascending oral doses (100, 250, 500, 750 mg) of JNJ 38224342 or matching placebo, administered for 14 consecutive days in healthy male or female volunteers
DRUGJNJ38224342/placebo
up to four (4) additional cohorts consisting of healthy male volunteers may be added
Sponsors
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Non-smokers * If male, willing to use an acceptable method of birth control for duration of study and for 90 days post study * Females must be post menopausal, surgically sterilized and cannot be pregnant or lactating (all parts of study) * Have a clinical history of allergic rhinitis during the ragweed pollen season and a positive skin test for ragweed allergy are required (for part 4 of study only)
Exclusion criteria
* Clinically significant medical illnesses, laboratory or ECG findings * History of allergy to aspirin or nonsteroidal anti-inflammatory drugs * history of alcohol or drug abuse within the last 5 years * HIV or Hepatitis B or C positive * Receipt of an investigational drug or use of an investigational medical device within the last month * History of asthma or severe respiratory infection or disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess safety and pharmacokinetics of single and multiple oral ascending doses of JNJ-38224342 with and without food in healthy volunteers and patients with seasonal allergies as determined by occurrence of adverse events, lab test results, vital sign | from the time of the first dose to 7-11 days after the last dose administered |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the results of biomarker assessments performed during Parts 2 and 4 of the trial. | from 7-11 days post the last administered dose |
| Evaluate the effectiveness of treatment based on nasal symptoms for Part 4. | from 7-11 days post the last administered dose |
Countries
Canada
Outcome results
None listed