Cystic fibrosis (CFTR F508del homozygous mutation) [DS:H00218] Cystic fibrosis (at least one mutation in CFTR) [DS:H00218]
Target
CFTR* [HSA_VAR:1080v1] [HSA:1080] [KO:K05031]
Pathway
hsa02010
ABC transporters
hsa04971
Gastric acid secretion
hsa04972
Pancreatic secretion
hsa04976
Bile secretion
Brite
Anatomical Therapeutic Chemical (ATC) classification [BR:br08303]
R RESPIRATORY SYSTEM
R07 OTHER RESPIRATORY SYSTEM PRODUCTS
R07A OTHER RESPIRATORY SYSTEM PRODUCTS
R07AX Other respiratory system products
R07AX31 Ivacaftor and tezacaftor
D11042 Tezacaftor and ivacaftor <US>
USP drug classification [BR:br08302]
Respiratory Tract/Pulmonary Agents
Cystic Fibrosis Agents
Conductance Regulator Potentiator
Tezacaftor/ Ivacaftor
D11042 Tezacaftor and ivacaftor
Target-based classification of drugs [BR:br08310]
Transporters
ABC transporters
ABCC subfamily
CFTR* [HSA_VAR:1080v1]
D11042 Tezacaftor and ivacaftor <US>
New drug approvals in the USA [br08319.html]
New molecular entities and new therapeutic biological products
D11042
New drug approvals in Europe [br08329.html]
European public assessment reports (EPAR) authorised medicine
D11042
New drug approvals in the USA, Europe and Japan [br08328.html]
Approval dates by FDA, EMA and PMDA
D11042
Pharmacogenomic biomarkers [br08341.html]
Germline mutations in genetic disorder treatments
D11042