Efficacy and Safety of FX201, a Novel Intra-Articular IL-1Ra Gene Therapy for Osteoarthritis Treatment, in a Rat Model.
Rebecca K SenterRogely BoyceMarko RepicEmily Walsh MartinMonika ChabicovskyGeneviève Langevin-CarpentierAgathe BédardNeil BodickPublished in: Human gene therapy (2022)
Osteoarthritis (OA) is a disabling, degenerative disease characterized by progressive cartilage and bone damage. There remains a need for local therapies that, following a single injection, can provide long-term pain relief and functional improvement and potentially delay disease progression. FX201 is a novel, intra-articular (IA), interleukin-1 receptor antagonist (IL-1Ra) gene therapy in development for the treatment of OA. In this study, we assessed the efficacy, biodistribution, and safety of helper-dependent adenovirus (HDAd)-ratIL-1Ra, the rat surrogate of FX201, and the biodistribution of FX201, in the anterior cruciate ligament transection (ACLT) rat OA model. A single IA injection of HDAd-ratIL-1Ra administered 7 days post-ACLT mitigated OA-related changes to cartilage, bone, and the synovial membrane at week 12 following surgery. Furthermore, FX201 and HDAd-ratIL-1Ra persisted for at least 92 days in the injected joint and proximal tissues with minimal evidence of vector spreading peripherally. Finally, HDAd-ratIL-1Ra showed a favorable safety profile without any local or systemic adverse effects. In conclusion, HDAd-ratIL-1Ra demonstrated local therapeutic and disease-modifying effects and was well tolerated, supporting further clinical development of FX201.
Keyphrases
- rheumatoid arthritis
- disease activity
- knee osteoarthritis
- gene therapy
- ankylosing spondylitis
- oxidative stress
- systemic lupus erythematosus
- minimally invasive
- multiple sclerosis
- bone mineral density
- gene expression
- pain management
- clinical trial
- pet imaging
- neuropathic pain
- body composition
- coronary artery bypass
- soft tissue
- genome wide
- postmenopausal women
- computed tomography
- dna methylation
- bone loss
- replacement therapy
- drug induced