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However, long-acting formulation still exhibited systemic side effects and is currently in the early stage, phase 1 or two clinical trial ( 2.2 Therapeutic advantages of Abs in AGA treatment mAb therapy was first administrated via intravenous (i.v.) route, has shifted towards to subcutaneous (s.c.) injections in order to be a more patient-friendly approach (Sanchez-Felix et al., 2020)

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in Orthopaedic Journal of Sports Medicine reviewing the complete BPC-157 musculoskeletal literature to June 2024 confirmed pre-clinical evidence of improved structural, biomechanical, and functional research applications across fracture, muscle, tendon, and ligamentous injury models

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Third, the compound has shown a favorable safety profile in preclinical studies