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topic_facet:"Quinolones"
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PubPharm (21)
1
A Phase 3, open-label, 96-week trial to study the safety, tolerability, and efficacy of tezacaftor/ivacaftor in children ≥ 6 years of age homozygous for F508del or heterozygous for F508del and a residual function CFTR variant
enthalten in:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
| 2022
von
Sawicki, G.
|
Chilvers, M.
|
McNamara, J.
| +10
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2
Long-term safety and efficacy of lumacaftor-ivacaftor therapy in children aged 6-11 years with cystic fibrosis homozygous for the F508del-CFTR mutation : a phase 3, open-label, extension study
enthalten in:
The Lancet. Respiratory medicine
| 2021
von
Chilvers, M.
|
Davies, J.
|
Milla, C.
| +5
ErratumIn: Lancet Respir Med. 2021 Apr;9(4):e38. - PMID 33607008
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3
Ivacaftor in People with Cystic Fibrosis and a 3849+10kb C→T or D1152H Residual Function Mutation
enthalten in:
Annals of the American Thoracic Society
| 2021
von
Kerem, E.
|
Cohen-Cymberknoh, M.
|
Tsabari, R.
| +13
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4
Ivacaftor in Infants Aged 4 to <12 Months with Cystic Fibrosis and a Gating Mutation. Results of a Two-Part Phase 3 Clinical Trial
enthalten in:
American journal of respiratory and critical care medicine
| 2021
von
Davies, J.
|
Wainwright, C.
|
Sawicki, G.
| +7
CommentIn: Am J Respir Crit Care Med. 2021 Mar 1;203(5):536-537. - PMID 33113333
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5
Entering the era of highly effective modulator therapies
enthalten in:
Pediatric pulmonology
| 2021
von
Dave, K.
|
Dobra, R.
|
Scott, S.
| +4
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6
A phase 3, double-blind, parallel-group study to evaluate the efficacy and safety of tezacaftor in combination with ivacaftor in participants 6 through 11 years of age with cystic fibrosis homozygous for F508del or heterozygous for the F508del-CFTR mutation and a residual function mutation
enthalten in:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
| 2021
von
Davies, J.
|
Sermet-Gaudelus, I.
|
Naehrlich, L.
| +10
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7
An open-label extension study of ivacaftor in children with CF and a CFTR gating mutation initiating treatment at age 2-5 years (KLIMB)
enthalten in:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
| 2019
von
Rosenfeld, M.
|
Cunningham, S.
|
Harris, W.
| +10
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8
GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients : An open-label, single-arm, phase 2a study (SAPHIRA1)
enthalten in:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
| 2019
von
Davies, J.
|
Van de Steen, O.
|
van Koningsbruggen-Rietschel, S.
| +8
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9
VX-659-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles
enthalten in:
The New England journal of medicine
| 2018
von
Davies, J.
|
Moskowitz, S.
|
Brown, C.
| +61
CommentIn: N Engl J Med. 2018 Oct 25;379(17):1671-1672. - PMID 30334694
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10
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL) : a phase 3 single-arm study
enthalten in:
The Lancet. Respiratory medicine
| 2018
von
Rosenfeld, M.
|
Wainwright, C.
|
Higgins, M.
| +38
CommentIn: Lancet Respir Med. 2018 Jul;6(7):483-484. - PMID 29886025
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Thema: Quinolones
Medienart
21
Aufsätze
21
E-Artikel
21
E-Ressourcen
Zeitschriftentitel
7
The Lancet. Respiratory medicine
5
Journal of cystic fibrosis : official journal o...
3
American journal of respiratory and critical ca...
3
The New England journal of medicine
1
Annals of the American Thoracic Society
1
Journal of the Royal Society of Medicine
1
Pediatric pulmonology
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Thema
21
Aminophenols
Quinolones
20
126880-72-6
20
1Y740ILL1Z
20
Cystic Fibrosis Transmembrane Conductance Regul...
20
Journal Article
20
ivacaftor
17
Research Support, Non-U.S. Gov't
12
Chloride Channel Agonists
11
CFTR protein, human
10
Multicenter Study
9
Benzodioxoles
9
Clinical Trial, Phase III
8
Randomized Controlled Trial
6
Indoles
6
tezacaftor
5
Drug Combinations
5
Ivacaftor
4
Aminopyridines
4
Cystic fibrosis
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Erscheinungszeitraum
6
2020-
15
2010-2019
Erscheinungsjahr(e)
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21
Englisch
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