Osteoporosis is a major disease burden - 22 million women and 5.5 million men aged between 50-84 years of age were estimated to have osteoporosis in the EU (2010 figures). Due to the EU’s aging population, this is expected to increase by 25% by 2025. The majority of these patients are treated with bisphosphonates (BPs), a drug that prevents bone loss. However, many patients remain on these drugs for years, if not for the remainder of their lives. Long-term BP therapy leads to over-suppression of bone remodelling, an impaired ability to repair skeletal micro-fractures, and increased skeletal fragility. As a result, there is an emerging and devastating challenge associated with prolonged BP use known as atypical femoral fracture (AFF). These fractures are excruciatingly painful and associated with high levels of morbidity and mortality. The intrinsic challenge with this medical problem is that these fractures are recalcitrant to treatment and there are currently no effective therapies available. During this MSCA fellowship, the goal was to design and develop a novel injectable therapeutic biomaterial technology that would stimulate repair of AFFs. The devise consisted of a thermoresponsive shear-thinning collagen-hydroxyapatite biomaterial that would serve as a regenerative template. In addition, therapeutics can be incorporated within the biomaterial to promote bone repair. The overall objective was to formulate and fabricate this injectable therapeutic device and to test the idea that continuous local delivery of parathyroid hormone (PTH(1-34)) would restore remodelling and facilitate bone healing.