NCT Number: NCT02447276
Study of REGN475 in Patients With Pain Due to Osteoarthritis of the Knee or Hip
The primary objective of this study is to evaluate the effectiveness of REGN475 compared to placebo in participants with pain due to osteoarthritis (OA) of the knee or hip and a history of inadequate joint pain relief or intolerance to current analgesic therapy.
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Notify MeKey information
Conditions
Age range
40 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2 / Phase 3
Primary location
Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
- Body mass index ≤39
- Clinical diagnosis of OA of the knee or hip
- History of inadequate pain relief or intolerance to analgesics used for OA
- Moderate to severe pain in the index joint
- History of regular use of analgesic medications for OA pain
- Willing to discontinue current non-steroidal anti-inflammatory drug (NSAID) and opioid pain medications
Key Exclusion Criteria:
- Other diseases that may involve index knee or hip, including inflammatory joint diseases, crystalline disease (gout or pseudogout), endocrinopathies, metabolic joint disease, lupus erythematosus, rheumatoid arthritis, joint infections, neuropathic disorders, avascular necrosis, Paget's disease, renal osteodystrophy or tumors
- History of osteonecrosis, destructive arthropathy (RPOA), hip dislocation, pathologic fractures, neuropathic joint arthropathy, knee dislocation or hip dislocation
- Trauma to the index joint in the 30 days before screening
- Active fibromyalgia, regional pain caused by lumbar or cervical compression with radiculopathy or other moderate to severe pain that may confound assessments or self-evaluation of the pain associated with OA
- Prior to the start of the study has received a recommendation for, or is scheduled for joint replacement surgery to be performed during the study period
- Presence of subchondral insufficiency fracture on screening films or MRI
- Received an intra-articular injection of hyaluronic acid in the affected index joint within 90 days prior to the screening visit
- Systemic (ie, oral or intramuscular) corticosteroids within 30 days prior to the screening visit. Intra-articular corticosteroids in the index joint within 12 weeks of the screening visit, or to any other joint within 30 days prior to the screening visit.
- History of autonomic neuropathy, diabetic neuropathy, or presence of clinically relevant peripheral neuropathy at the time of screening
- Women of childbearing potential who have a positive pregnancy test result, or who do not have their pregnancy test results at baseline
- Pregnant or breastfeeding women
Treatment and study plan
Placebo
DrugPrimary outcomes
-
The primary endpoint in the study is the change from baseline to week 16 in the Western Ontario and McMaster Osteoarthritis Index (WOMAC) pain subscale score.
Time frame: Baseline to week 16
Secondary outcomes
-
Change from baseline to week 16 in the WOMAC physical function subscale score
Time frame: Baseline to week 16
-
Change from baseline to week 16 in the Patient Global Assessment score
Time frame: Baseline to week 16
-
Incidence of treatment-emergent adverse events (TEAEs)
Time frame: Baseline to week 36 (end of study)
-
Incidence of anti-REGN475 antibody development
Time frame: Baseline to week 36 (end of study)
Sponsors and collaborators
Lead sponsor
Regeneron Pharmaceuticals
Industry
Registry information
Official study title
A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to Evaluate the Efficacy and Safety of REGN475 in Patients With Pain Due to Osteoarthritis of the Knee or Hip
Important dates
- Study start
- 2015
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- May 18, 2015
- Registry last updated
- Mar 27, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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