Filter the drugs by the phase of research, how they help and the responsive mutations.

Cystic fibrosis is a genetic disease caused by mutations in the CFTR gene. Browse the database of drugs treating specific mutations compiled by the AIM tool.
Drug Marketed as Description Phase of research How it helps
Ataluren Translarna™

Suppresses premature stop mutation

EMA-approved for Other Purpose Restore CFTR Function
Curcumin

CFTR potentiator

Accessible Dietary Supplement Restore CFTR Function
Elexacaftor Trikafta™

CFTR corrector

FDA-approved for Cystic Fibrosis Restore CFTR Function
G418

Aminoglycoside antibiotic capable of translational readthrough

Pre-clinical Restore CFTR Function
Gentamicin 

Aminoglycoside antibiotic capable of translational readthrough

FDA-/EMA-approved for Other Purpose Restore CFTR Function
Ivacaftor Kalydeco® (ivacaftor), Orkambi® (ivacaftor/lumacaftor), Symdeko® (ivacaftor/tezacaftor), Symkevi® (ivacaftor/tezacaftor), Trikafta™(elexacaftor/tezacaftor/ivacaftor)

CFTR potentiator

FDA-/EMA-approved for Cystic Fibrosis Restore CFTR Function
NB30 

Aminoglycoside capable of translational readthrough

Pre-clinical Restore CFTR Function
NB54

Aminoglycoside capable of translational readthrough

Pre-clinical Restore CFTR Function
Paromomycin

Aminoglycoside capable of translational readthrough

FDA-/EMA-approved for Other Purpose Restore CFTR Function
Tezacaftor Symdeko® (ivacaftor/tezacaftor), Symkevi® (ivacaftor/tezacaftor), Trikafta™(elexacaftor/tezacaftor/ivacaftor)

CFTR corrector

FDA-/EMA-approved for Cystic Fibrosis Restore CFTR Function