
Symkevi - European Medicines Agency (EMA)
Symkevi is a medicine used to treat cystic fibrosis in patients aged 6 years and above. Cystic fibrosis is an inherited disease that has severe effects on the lungs, the digestive system and …
Symkevi(tezacaftor/ivacaftor)FDA官方说明书 - 知乎 - 知乎专栏
SYMDEKO是tezacaftor和ivacaftor的组合,适用于治疗6岁及以上的F508del突变纯合子或对tezacaftor / ivacaftor有反应的囊性纤维化跨膜电导调节剂(CFTR)基因中至少有一种突变的患 …
What is Symkevi and what is it used for? Symkevi is a medicine used to treat cystic fibrosis in patients aged 6 years and above. Cystic fibrosis is an inherited disease that has severe effects …
Symkevi说明书-价格-功效与作用-副作用 - pidrug.com
2023年6月5日 · 2018年11月2日,Vertex 制药宣布欧盟批准其新型两药复方药物 Symkevi(tezacaftor/ivacaftor),这次批准有助于该药物用于治疗更多的囊性纤维化(CF)患 …
Symkevi 100 mg/150 mg film-coated tablets - Summary of …
2025年1月13日 · Symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (CF) aged 6 years and older who are homozygous for …
欧盟批准 Vertex 囊性纤维化药物 Symkevi - 丁香园
2018年11月5日 · PMLiVE 于 11 月 2 日报道,Vertex 制药宣布欧盟批准其新型两药复方药物 Symkevi(tezacaftor/ivacaftor),这次批准有助于该药物用于治疗更多的囊性纤维化(CF) …
Symkevi is indicated in a combination regimen with ivacaftor tablet s for the treatment of patients with cystic fibrosis (CF) aged 6 years and older who are homozygous for the F508del mutation
Tezacaftor / ivacaftor (Symkevi) for the treatment of cystic fibrosis ...
2020年10月29日 · The fixed-dose combination of tezacaftor / ivacaftor (trade name: Symkevi) has been approved in Germany since October 2018 for the treatment of cystic fibrosis in people …
Symkevi - Vertex Pharmaceuticals (Ireland) Limited - 药物在线
Symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (CF) aged 6 years and older who are homozygous for the F508del mutation …
Tezacaftor with ivacaftor | Drugs | BNF | NICE
Tezacaftor with ivacaftor (Symkevi®) in combination with ivacaftor for the treatment of patients with cystic fibrosis aged 6 years and older who are homozygous for the F508del mutation or …
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