Study to Characterize the PK and Local Extent and Duration of Exposure From FX006 in Patients With OA of the Knee
Status: | Completed |
---|---|
Conditions: | Arthritis, Osteoarthritis (OA) |
Therapuetic Areas: | Rheumatology |
Healthy: | No |
Age Range: | 40 - Any |
Updated: | 1/14/2018 |
Start Date: | November 2015 |
End Date: | September 2016 |
An Open-label, Single Administration Study to Characterize the Systemic Pharmacokinetics and Local Extent and Duration of Exposure of Triamcinolone Acetonide From FX006 in Patients With Osteoarthritis of the Knee
The objectives of this study were to characterize the local extent and duration of exposure
of TA from FX006 and TCA IR, characterize the systemic PK of FX006 and TCA IR, and assess the
safety and general tolerability of a single 5 mL IA injection of 32 mg FX006 relative to 40
mg of TCA IR in patients with OA of the knee.
of TA from FX006 and TCA IR, characterize the systemic PK of FX006 and TCA IR, and assess the
safety and general tolerability of a single 5 mL IA injection of 32 mg FX006 relative to 40
mg of TCA IR in patients with OA of the knee.
This study employed an open-label, single administration design and was conducted in male and
female patients ≥40 years of age with OA of the knee.
Patients were enrolled sequentially with at least 10 patients per cohort as follows:
Cohort A: FX006 32 mg, Final Visit at Week 20 Cohort B: FX006 32 mg, Final Visit at Week 16
Cohort C: FX006 32 mg, Final Visit at Week 12 Cohort D: FX006 32 mg, Final Visit at Week 6
Cohort E: FX006 32 mg, Final Visit at Week 1 Cohort F: TCA IR 40 mg, Final Visit Week 6
Each patient was screened to confirm eligibility and assigned to a cohort on Day 1/baseline.
Each patient was evaluated for safety during his/her participation in the study at 6, 12, 16,
or 20 weeks following a single IA injection depending on the assigned Cohort, and plasma and
synovial fluid was collected for drug concentration measurements.
Safety and tolerability was assessed by physical examinations, index knee examinations, vital
signs, clinical laboratory evaluations, and adverse events (AEs).
No efficacy assessments were employed in this study.
female patients ≥40 years of age with OA of the knee.
Patients were enrolled sequentially with at least 10 patients per cohort as follows:
Cohort A: FX006 32 mg, Final Visit at Week 20 Cohort B: FX006 32 mg, Final Visit at Week 16
Cohort C: FX006 32 mg, Final Visit at Week 12 Cohort D: FX006 32 mg, Final Visit at Week 6
Cohort E: FX006 32 mg, Final Visit at Week 1 Cohort F: TCA IR 40 mg, Final Visit Week 6
Each patient was screened to confirm eligibility and assigned to a cohort on Day 1/baseline.
Each patient was evaluated for safety during his/her participation in the study at 6, 12, 16,
or 20 weeks following a single IA injection depending on the assigned Cohort, and plasma and
synovial fluid was collected for drug concentration measurements.
Safety and tolerability was assessed by physical examinations, index knee examinations, vital
signs, clinical laboratory evaluations, and adverse events (AEs).
No efficacy assessments were employed in this study.
Inclusion Criteria:
- Written consent to participate in the study
- Willingness and ability to comply with the study procedures and visit schedules and
ability to follow verbal and written instructions
- Symptoms associated with OA of the knee for ≥ 6 months prior to Screening (patient
reported is acceptable)
- Currently meets American College of Rheumatology (ACR) Criteria (clinical and
radiological) for OA
- Index knee pain for >15 days over the last month (as reported by the patient)
- Body mass index (BMI) ≤ 40 kg/m2
- Ambulatory and in good general health
Exclusion Criteria:
- Fibromyalgia, Reiter's syndrome, rheumatoid arthritis, psoriatic arthritis, ankylosing
spondylitis, or arthritis associated with inflammatory bowel disease
- History of infection in the index knee joint
- Clinical signs and symptoms of active knee infection or crystal disease of the index
knee within 1 month of Screening
- Presence of surgical hardware or other foreign body in the index knee
- Unstable joint within 12 months of Screening
- IA corticosteroid (investigational or marketed) in any joint within 6 months of
Screening
- IA hyaluronic acid (investigational or marketed) in the index knee within 6 months of
Screening
- Intravenous or Intramuscular corticosteroids (investigational or marketed) within 3
months of Screening
- Oral corticosteroids (investigational or marketed) within 1 month of Screening
- Inhaled, intranasal or topical corticosteroids (investigational or marketed) within 2
weeks of Screening
- Any other IA investigational drug/biologic use within 6 months of Screening or 5
half-lives (whichever is longer)
- Prior use of FX006
- Women of child-bearing potential not using effective contraception or who are pregnant
or nursing
We found this trial at
4
sites
Click here to add this to my saved trials
Duncansville, Pennsylvania 16635
Phone: 814-693-0400
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials