A patent review on cathepsin K inhibitors to treat osteoporosis (2011 - 2021).
Fernanda R RochoVinícius BonattoRafael da Fonseca LameiroJeronimo LameiraAndrei LeitãoCarlos Alberto MontanariPublished in: Expert opinion on therapeutic patents (2022)
As one of the most potent lysosomal proteins whose primary function is to mediate bone resorption, cathepsin K remains an excellent target for therapeutic intervention. Nevertheless, there is no record of any approved drug that targets CatK. The most notable cases of drug candidates targeting CatK were balicatib and odanacatib, which reached Phase II and III clinical trials, respectively, but did not enter the market. Further developments include exploring new chemical entities beyond the nitrile-based chemical space, with improved ADME and safety profiles. In addition, CatK's role in cancer immunoexpression and its involvement in the pathophysiology of osteo- and rheumatoid arthritis have raised the race to develop activity-based probes with excellent potency and selectivity.
Keyphrases
- phase ii
- clinical trial
- rheumatoid arthritis
- open label
- bone mineral density
- papillary thyroid
- postmenopausal women
- randomized controlled trial
- phase iii
- small molecule
- bone loss
- molecular docking
- placebo controlled
- disease activity
- squamous cell carcinoma
- single molecule
- cancer therapy
- study protocol
- living cells
- lymph node metastasis
- childhood cancer
- emergency department
- bone regeneration
- idiopathic pulmonary fibrosis
- systemic lupus erythematosus
- systemic sclerosis
- molecular dynamics simulations
- fluorescence imaging
- fluorescent probe