Study to Evaluate a Procedure for Intra-articular Injection of FX006 in Patients With Osteoarthritis of the Hip

Completed · Phase 2

Conditions studied: Osteoarthritis, Hip

In brief

This is a multi-center, single-arm, open-label study of FX006 in patients with hip OA. A maximum number of approximately 30 patients may be enrolled in this protocol. All enrolled patients will receive a single intra-articular (IA) injection of FX006.

Key facts

Study ID

NCT04065074

Run by

Pacira Pharmaceuticals, Inc

People needed

16

Starts

2019-07-30

Expected to finish

2019-12-30

Last updated by the study team

2024-01-24

Who can join

Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Willingness and ability to comply with the study procedures and visit schedules and ability to follow verbal and written instructions
• Patients 40 to 80 years of age, inclusive, on the day of consent
• Body Mass Index (BMI) ≤ 40 kg/m\^2
• Has a documented clinical diagnosis of unilateral or bilateral hip OA for at least six months
• Kellgren-Lawrence (KL) Grade 2 or 3 in the index hip as confirmed by local read of X-ray obtained during Screening or ≤ 6 months of Screening visit
• Has clinically significant pain in the index hip

You may not qualify if…

• Has a history of hypersensitivity to triamcinolone acetonide, PLGA or lidocaine
• Is receiving anticoagulants (including warfarin, dabigatran, rivaroxaban, apixaban or low molecular weight heparin, ritonavir or cobicistat)
• Has had any previous surgery on the index hip
• Presence of surgical hardware or other foreign body in the index hip
• Has a history of infection of the index hip
• Has a diagnosis of other disorders in the index hip that can cause pain
• Has received any intra-articular injection in the index hip of corticosteroids, investigational (including FX006) or marketed (including Zilretta®) within the 3 months prior to Screening
• Has had trauma to the index hip in the past 3 months requiring immobilization
• Has a history or evidence of active or latent systemic fungal or mycobacterial infection (including tuberculosis), or of ocular herpes simplex
• Has within the past 3 months received corticosteroids by mouth, or by parenteral injection. Multiple courses or chronic intermittent use of inhaled, intranasal, or topical steroids is also exclusionary. Single courses of 14 days or less by those routes are permitted
• Has, at screening, or any time prior to day of scheduled injection (Day 1), clinical suspicion of local or systemic infection, including any infection in the index leg.
• Has a history of or active significant concomitant illness (known or suspected)
• Any bacterial or viral infection requiring parental antibiotics within 4 weeks of Day 1 or oral antibiotics within 2 weeks of Day 1
• Is a woman who is pregnant, nursing, lactating, or plans to become pregnant during the study
• Is a man who plans to conceive during the study

Where it is running

• Noble Clinical Research — Tucson, Arizona, United States
• Hope Clinical Research — Canoga Park, California, United States
• Biosolutions Clinical Research Center — La Mesa, California, United States
• Dream Team Clinical Research — Pomona, California, United States
• Lenox Hill Hospital — New York, New York, United States

Full record on ClinicalTrials.gov

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