ATC Group: M05BX Other drugs affecting bone structure and mineralization

The World Health Organization's ATC classification organizes medical drugs based on therapeutic properties, chemical composition, and anatomy. It helps make essential medicines readily available globally and is widely used in the pharmaceutical industry.

Position of M05BX in the ATC hierarchy

Level Code Title
1 M Musculo-skeletal system
2 M05 Drugs for treatment of bone diseases
3 M05B Drugs affecting bone structure and mineralization
4 M05BX Other drugs affecting bone structure and mineralization

Group M05BX contents

Code Title
M05BX01 Ipriflavone
M05BX02 Aluminium chlorohydrate
M05BX03 Strontium ranelate
M05BX04 Denosumab
M05BX05
M05BX06
M05BX07
M05BX08
M05BX53

Active ingredients in M05BX

Active Ingredient Description
Burosumab

Burosumab is a recombinant human monoclonal antibody (IgG1) that binds to and inhibits the activity of fibroblast growth factor 23 (FGF23). By inhibiting FGF23, burosumab increases tubular reabsorption of phosphate from the kidney and increases serum concentration of 1,25 dihydroxy-Vitamin D.

Denosumab

Denosumab is a human monoclonal antibody (IgG2) that targets and binds with high affinity and specificity to RANKL, preventing activation of its receptor, RANK, on the surface of osteoclast precursors and osteoclasts. Prevention of the RANKL/RANK interaction inhibits osteoclast formation, function and survival, thereby decreasing bone resorption in cortical and trabecular bone.

Menatetrenone
Romosozumab

Romosozumab is a humanized monoclonal antibody (IgG2) that binds and inhibits sclerostin, thereby increasing bone formation due to the activation of bone lining cells, increasing bone matrix production by osteoblasts, and recruitment of osteoprogenitor cells. Additionally, romosozumab results in changes to expression of osteoclast mediators, thereby decreasing bone resorption.

Strontium ranelate

In vitro, strontium ranelate increases bone formation in bone tissue culture as well as osteoblast precursor replication and collagen synthesis in bone cell culture and reduces bone resorption by decreasing osteoclast differentiation and resorbing activity. This results in a rebalance of bone turnover in favour of bone formation.

Vosoritide

Vosoritide is a modified type C natriuretic peptide (CNP). In patients with achondroplasia, endochondral bone growth is negatively regulated due to a gain of function mutation in fibroblast growth factor receptor 3 (FGFR3). Binding of vosoritide to natriuretic peptide receptor-B (NPR-B) antagonises FGFR3 downstream signalling by inhibiting the extracellular signal-regulated kinases 1 and 2 (ERK1/2) in the mitogen-activated protein kinase (MAPK) pathway at the level of rapidly accelerating fibrosarcoma serine/threonine protein kinase (RAF-1). As a result, vosoritide, like CNP, acts as a positive regulator of endochondral bone growth as it promotes chondrocyte proliferation and differentiation.

Related product monographs

Title Information Source Document Type  
CRYSVITA Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
CRYSVITA Solution for injection European Medicines Agency (EU) MPI, EU: SmPC
EVENITY Solution for injection European Medicines Agency (EU) MPI, EU: SmPC
EVENITY Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
JUBBONTI Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
PROLIA Solution for injection European Medicines Agency (EU) MPI, EU: SmPC
VOXZOGO Powder and solvent for solution for injection European Medicines Agency (EU) MPI, EU: SmPC
WYOST Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
WYOST Solution for injection European Medicines Agency (EU) MPI, EU: SmPC