M
mememanw24
Iron
- Joined
- May 7, 2025
- Posts
- 50
- Reputation
- 37
Nintedanib is available in my country and hits FGFR3 while infigratinib is basically impossible to get.
Infigratinib has real achondroplasia trial data showing increased growth velocity by inhibiting FGFR3 over-signaling.
Since nintedanib also inhibits FGFR3 (though broader/weaker), could it give similar bone growth benefits in normal teens with open plates?
Or is the FGFR3 affinity too low at safe doses (100–200 mg/day cancer dose) and it’s cope compared to infigratinib?
Infigratinib has real achondroplasia trial data showing increased growth velocity by inhibiting FGFR3 over-signaling.
Since nintedanib also inhibits FGFR3 (though broader/weaker), could it give similar bone growth benefits in normal teens with open plates?
Or is the FGFR3 affinity too low at safe doses (100–200 mg/day cancer dose) and it’s cope compared to infigratinib?