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A Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of JNJ-39439335 in Patients With Osteoarthritis

NCT ID: NCT01343303

Last Updated: 2012-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

43 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-03-31

Study Completion Date

2011-12-31

Brief Summary

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The purpose of this study is to evaluate the safety of multiple oral doses of JNJ-39439335 and to assess how JNJ-39439335 is absorbed (taken in), distributed, metabolized (broken down), and eliminated from the body (referred to as pharmacokinetics) in osteoarthritis patients. This study will also assess the effectiveness of JNJ-39439335 on pain.

Detailed Description

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This will be a double-blind (patient and study staff will not know the identity of assigned treatment), randomized (assignment to 1 to 3 treatment groups will be by chance, like "flipping a coin"), placebo-controlled, multiple dose study conducted at up to two clinical sites. Up to 42 patients with osteoarthritis of the knee will be enrolled in 3 cohorts (Cohort 1 to 3). Additional cohorts (up to 14 patients per cohort) may be added after completion of Cohort 3. The study consists of eligibility screening, a treatment phase, and 4 follow-up visits. The study duration for each patient will be approximately 10 weeks. Patients safety will be closely monitored during the study by review of adverse events, electrocardiograms, vital signs (including oral temperature), clinical laboratory tests, and physical examinations. During specified study visits, blood samples will be collected for pharmacokinetics, pharmacodynamics (inpatient patients), and pharmacogenomic (optional) evaluations of JNJ-39439335. The effectiveness of JNJ-39439335 will be evaluated by assessing pain using an 11-point numerical rating scale and by the Western Ontario and McMaster Osteoarthritis Index. In Cohort 1 and 2, all patients will take their study medication orally, twice a day for 21 days. The treatment groups for Cohort 1 are JNJ-39439335 10 mg, naproxen 500 mg every 12 hours, and placebo. The treatment groups for Cohort 2 are JNJ-39439335 25 mg, naproxen 500 mg every 12 hours, and placebo. The treatment groups for Cohort 3 will be determined based on the results of Cohort 1 and 2.

Conditions

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Osteoarthritis, Knee

Keywords

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Osteoarthritis, knee knee pain pain measurement

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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001

JNJ-39439335 2 x 5 mg tablets once daily for 21 days

Group Type EXPERIMENTAL

JNJ-39439335

Intervention Type DRUG

2 x 5 mg tablets once daily for 21 days

002

JNJ-39439335 2 x 25 mg tablets once daily for 21 days

Group Type EXPERIMENTAL

JNJ-39439335

Intervention Type DRUG

2 x 25 mg tablets once daily for 21 days

003

Naproxen 500 mg capsule every 12 hours for 21 days

Group Type OTHER

Naproxen

Intervention Type DRUG

500 mg capsule every 12 hours for 21 days

004

Placebo Placebo tablet/capsule every 12 hours for 21 days

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Placebo tablet/capsule every 12 hours for 21 days

Interventions

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Placebo

Placebo tablet/capsule every 12 hours for 21 days

Intervention Type DRUG

JNJ-39439335

2 x 25 mg tablets once daily for 21 days

Intervention Type DRUG

Naproxen

500 mg capsule every 12 hours for 21 days

Intervention Type DRUG

JNJ-39439335

2 x 5 mg tablets once daily for 21 days

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Nonsmoker \>= 6 months prior to first dose
* body mass index (BMI) \<= 36 kg/m2
* Meet American College of Rheumatology (ACR) clinical classification criteria for osteoarthritis of knee by meeting at least 3 of the following: age \> 50, morning stiffness \< 30 minutes, crepitus on active motion, bony tenderness, bony enlargement, no palpable warmth of synovium
* Has Functional Class I-III osteoarthritis (OA) of knee with continuing OA-knee joint pain \>= 5 days/week x 3 months prior to screening, and has been taking a non-opioid analgesic for OA knee pain daily for \>=5 days prior to screening with benefit
* Otherwise healthy based on physical exam, medical history, vital signs, 12-lead electrocardiogram (ECG), can clinical laboratory tests
* Women must be postmenopausal or surgically sterile.

Exclusion Criteria

* Oral temperature \>37.5 deg C at Screening or Day -1
* Failure of burn prevention measures quiz at Screening
* patients with occupations or hobbies in which they are routinely exposed to situations in which they could sustain burns
* orthopedic and/or prosthetic device on target knee joint
* Significant pain outside the target knee, including significant hip or back pain (bilateral knee OA is permitted)
* Unable to discontinue prior analgesic medications/non-steroidal antiinflammatory drugs (NSAIDS) other than paracetamol during the study
* Surgical intervention for any pain within 3 months prior to screening or has plans for surgical intervention while in the study
* History of prior diagnosis of inflammatory arthritis (including rheumatoid arthritis)
* Treatment with local corticosteroid injections or viscosupplementation in target joint, or use of oral or intramuscular corticosteroids, within 3 months prior to Screening
* History of active peptic ulceration, active dyspepsia, gastrointestinal bleeding, Crohn's disease, ulcerative colitis, chronic diarrhea esophageal, and gastric or duodenal ulcer within 3 months prior to screening or any other condition, which in the Investigator's opinion, precludes use of an NSAID.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Janssen Research & Development, LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Janssen Research & Development, LLC

Principal Investigators

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Janssen Research & Development, LLC C. Clinical Trial

Role: STUDY_DIRECTOR

Janssen Research & Development, LLC

Locations

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George, , South Africa

Site Status

Countries

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South Africa

Other Identifiers

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39439335EDI1014

Identifier Type: OTHER

Identifier Source: secondary_id

CR018292

Identifier Type: -

Identifier Source: org_study_id