Fasitibant Intra-articular Injection in Patients With Symptomatic Osteoarthritis of the Knee
| Status: | Completed |
|---|---|
| Conditions: | Arthritis, Osteoarthritis (OA) |
| Therapuetic Areas: | Rheumatology |
| Healthy: | No |
| Age Range: | 40 - 80 |
| Updated: | 4/21/2016 |
| Start Date: | April 2014 |
| End Date: | January 2015 |
A Double-blind, Randomised, Placebo-controlled, Four Parallel Arm, Dose-finding Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Single Intra-articular Injections of Fasitibant in Patients With Symptomatic Osteoarthritis of the Knee.
This study is designed as a double-blind, randomised, placebo-controlled, four parallel arm,
dose-finding study, to be conducted in approximately 26 sites, to evaluate the efficacy,
safety, tolerability, and pharmacokinetics of single intra-articular (IA) injections of
fasitibant in patients with symptomatic osteoarthritis (OA) of the knee.
Approximately 400 male and female patients 40-80 years old, with BMI < 30 kg/m² and with a
clinical diagnosis of symptomatic primary osteoarthritis of the knee will be randomised to a
total of 4 treatment arms. Each arm includes a single intra-articular injection of one of
three dosages of fasitibant (low, intermediate and high dose) OR placebo. The randomisation
ratio will be 1:1:1:1.
The primary efficacy variable will be the change of the Western Ontario and McMaster
Universities Visual Analogue Scale 3.1 A (WOMAC VA 3.1 A) (total pain) subscore from
baseline up to 2 weeks after randomisation. Safety will be assessed by monitoring adverse
events and clinical laboratory tests; local tolerability at the injection site will also be
assessed. In addition, the population pharmacokinetics and the exposure-response
relationship will be evaluated.
The individual experimental clinical phase will last up to maximal 15 weeks encompassing 7
planned visits at site, including screening, randomisation, 4 follow-up visits and the End
of study visit.
dose-finding study, to be conducted in approximately 26 sites, to evaluate the efficacy,
safety, tolerability, and pharmacokinetics of single intra-articular (IA) injections of
fasitibant in patients with symptomatic osteoarthritis (OA) of the knee.
Approximately 400 male and female patients 40-80 years old, with BMI < 30 kg/m² and with a
clinical diagnosis of symptomatic primary osteoarthritis of the knee will be randomised to a
total of 4 treatment arms. Each arm includes a single intra-articular injection of one of
three dosages of fasitibant (low, intermediate and high dose) OR placebo. The randomisation
ratio will be 1:1:1:1.
The primary efficacy variable will be the change of the Western Ontario and McMaster
Universities Visual Analogue Scale 3.1 A (WOMAC VA 3.1 A) (total pain) subscore from
baseline up to 2 weeks after randomisation. Safety will be assessed by monitoring adverse
events and clinical laboratory tests; local tolerability at the injection site will also be
assessed. In addition, the population pharmacokinetics and the exposure-response
relationship will be evaluated.
The individual experimental clinical phase will last up to maximal 15 weeks encompassing 7
planned visits at site, including screening, randomisation, 4 follow-up visits and the End
of study visit.
Inclusion Criteria:
- Male or female patients aged 40 to 80 years with BMI < 30 kg/m²
- Patient with Kellgren-Lawrence Grade 2 to 3, symptomatic primary osteoarthritis at
the index knee (ACR criteria), for which an IA treatment is indicated
- Pain of moderate to severe intensity, even if treated with chronic doses of non
steroidal antinflammatory drugs
Exclusion Criteria:
- History of hypersensitivity/allergy to drugs including paracetamol and to
disinfectants
- Any pharmacological treatment of concomitant disease(s) started or changed during 4
weeks prior to randomisation, or likely to be changed during the course of the study
- Use of systemic or topical corticosteroids > 10 mg prednisolone equivalent per day,
or immunosuppressant drugs
- Current use of any pain or OA medication (e.g. NSAIDs, COX-2 inhibitors, analgesics,
antidepressive agents), including topical treatments
- Viscosupplementation to the target knee administered < 4 months prior to
randomisation and/or scheduled during the course of the study
- Evidence of clinically significant hepatic disease or of moderate or severe renal
insufficiency
- Current use of any medications that are substrate of CYP3A4 and/or moderate or strong
CYP3A4 inhibitors
- Patients with any clinically relevant or unstable disease, or malignant neoplasms
that, in the opinion of the Investigator, may pose the patient at risk, or confound
the efficacy and safety results of the study
- Patients with any clinically relevant abnormal safety laboratory test results, and/or
abnormalities in vital signs, and/or ECG parameters
- Pregnant and breastfeeding women
- Any sign of significant immunodeficiency, systemic infection, knee infection or knee
bursitis
- Patients with bleeding diathesis or on therapy with anticoagulants
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