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