Osteoporosis is a systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue, with a subsequent increase in bone fragility and susceptibility to fracture. Osteoporosis is one of the most common and debilitating chronic diseases, and a global health concern with a high prevalence not only in Western countries, but also in Asia and Latin America. Most efficacious anti-osteoporotic treatments either inhibit bone resorption like bisphosphonates or denosumab or increase bone formation like teripartide an anabolic agent. Anti-osteoporotic drugs have demonstrated safety and efficacy with an increase in bone mass and a decrease of fracture risk (at the hip) by 30 to 50% after 3 years of treatment (Black et al., 1996; Neer et al., 2001; Meunier et al., 2004). Despite the availability of pharmacological treatments, osteoporosis remains a significant health problem for patients who do not respond to the available treatments or fail to comply with their regimens. The present phase 2a study aims to demonstrate the safety and efficacy of PREOB®, a proprietary population of autologous osteoblastic cells, in the treatment of osteoporotic patients who do not respond to pharmacological treatments.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Each patient will undergo a single intravenous administration of PREOB®.
Investigating site BE01
Anderlecht, Belgium
Cell biodistribution after intravenous infusion as assessed by SPECT/CT scan
Time frame: 72 hours
Potential occurrence of any AE or SAE, related to the product, using patient open non-directive questionnaire, physical examination and laboratory measurements
Time frame: 12 months
Pain measured by the Visual Analogue Scale
Time frame: 12 months
Well-being score using SF-36 questionnaire
Time frame: 12 months
Occurrence of new vertebral fractures as assessed by X-ray
Time frame: 12 months
Bone mineral density evolution as assessed by Dual-energy X-ray absorptiometry (DEXA)
Time frame: 12 months
Measurement of bone formation and resorption markers
Time frame: 12 months
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