These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
432 related articles for article (PubMed ID: 35633605)
1. Who are the 10%? - Non eligibility of cystic fibrosis (CF) patients for highly effective modulator therapies. Desai M; Hine C; Whitehouse JL; Brownlee K; Charman SC; Nagakumar P Respir Med; 2022 Aug; 199():106878. PubMed ID: 35633605 [TBL] [Abstract][Full Text] [Related]
2. Corrector therapies (with or without potentiators) for people with cystic fibrosis with class II CFTR gene variants (most commonly F508del). Heneghan M; Southern KW; Murphy J; Sinha IP; Nevitt SJ Cochrane Database Syst Rev; 2023 Nov; 11(11):CD010966. PubMed ID: 37983082 [TBL] [Abstract][Full Text] [Related]
3. Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week, multicentre, randomised, double-blind, active-controlled, phase 3b trial. Sutharsan S; McKone EF; Downey DG; Duckers J; MacGregor G; Tullis E; Van Braeckel E; Wainwright CE; Watson D; Ahluwalia N; Bruinsma BG; Harris C; Lam AP; Lou Y; Moskowitz SM; Tian S; Yuan J; Waltz D; Mall MA; Lancet Respir Med; 2022 Mar; 10(3):267-277. PubMed ID: 34942085 [TBL] [Abstract][Full Text] [Related]
4. Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial. Heijerman HGM; McKone EF; Downey DG; Van Braeckel E; Rowe SM; Tullis E; Mall MA; Welter JJ; Ramsey BW; McKee CM; Marigowda G; Moskowitz SM; Waltz D; Sosnay PR; Simard C; Ahluwalia N; Xuan F; Zhang Y; Taylor-Cousar JL; McCoy KS; Lancet; 2019 Nov; 394(10212):1940-1948. PubMed ID: 31679946 [TBL] [Abstract][Full Text] [Related]
5. Patients eligible for modulator drugs: Data from cystic fibrosis registry of Turkey. Çobanoğlu N; Özçelik U; Çakır E; Şişmanlar Eyüboğlu T; Pekcan S; Cinel G; Yalçın E; Kiper N; Emiralioğlu N; Şen V; Şen HS; Ercan Ö; Çokuğraş H; Kılınç AA; Al Shadfan LM; Yazan H; Altıntaş DU; Karagöz D; Demir E; Kartal Öztürk G; Bingöl A; Başaran AE; Sapan N; Çekiç Ş; Çelebioğlu E; Aslan AT; Gürsoy TR; Tuğcu G; Özdemir A; Harmancı K; Yıldırım GK; Köse M; Hangül M; Tamay Z; Süleyman A; Yüksel H; Yılmaz Ö; Özcan G; Topal E; Can D; Korkmaz Ekren P; Çaltepe G; Kılıç M; Özdoğan Ş; Doğru D Pediatr Pulmonol; 2020 Sep; 55(9):2302-2306. PubMed ID: 32453906 [TBL] [Abstract][Full Text] [Related]
6. Improvement in Lung Clearance Index and Chest Computed Tomography Scores with Elexacaftor/Tezacaftor/Ivacaftor Treatment in People with Cystic Fibrosis Aged 12 Years and Older - The RECOVER Trial. McNally P; Lester K; Stone G; Elnazir B; Williamson M; Cox D; Linnane B; Kirwan L; Rea D; O'Regan P; Semple T; Saunders C; Tiddens HAWM; McKone E; Davies JC; Am J Respir Crit Care Med; 2023 Nov; 208(9):917-929. PubMed ID: 37703083 [No Abstract] [Full Text] [Related]
7. Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two Graeber SY; Vitzthum C; Pallenberg ST; Naehrlich L; Stahl M; Rohrbach A; Drescher M; Minso R; Ringshausen FC; Rueckes-Nilges C; Klajda J; Berges J; Yu Y; Scheuermann H; Hirtz S; Sommerburg O; Dittrich AM; Tümmler B; Mall MA Am J Respir Crit Care Med; 2022 Mar; 205(5):540-549. PubMed ID: 34936849 [No Abstract] [Full Text] [Related]
8. Real-life impact of highly effective CFTR modulator therapy in children with cystic fibrosis. Olivier M; Kavvalou A; Welsner M; Hirtz R; Straßburg S; Sutharsan S; Stehling F; Steindor M Front Pharmacol; 2023; 14():1176815. PubMed ID: 37229253 [No Abstract] [Full Text] [Related]
9. The preclinical discovery and development of the combination of ivacaftor + tezacaftor used to treat cystic fibrosis. Guerra L; Favia M; Di Gioia S; Laselva O; Bisogno A; Casavola V; Colombo C; Conese M Expert Opin Drug Discov; 2020 Aug; 15(8):873-891. PubMed ID: 32290721 [TBL] [Abstract][Full Text] [Related]
10. Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two Graeber SY; Renz DM; Stahl M; Pallenberg ST; Sommerburg O; Naehrlich L; Berges J; Dohna M; Ringshausen FC; Doellinger F; Vitzthum C; Röhmel J; Allomba C; Hämmerling S; Barth S; Rückes-Nilges C; Wielpütz MO; Hansen G; Vogel-Claussen J; Tümmler B; Mall MA; Dittrich AM Am J Respir Crit Care Med; 2022 Aug; 206(3):311-320. PubMed ID: 35536314 [No Abstract] [Full Text] [Related]
11. Tezacaftor/Ivacaftor in Subjects with Cystic Fibrosis and F508del/F508del-CFTR or F508del/G551D-CFTR. Donaldson SH; Pilewski JM; Griese M; Cooke J; Viswanathan L; Tullis E; Davies JC; Lekstrom-Himes JA; Wang LT; Am J Respir Crit Care Med; 2018 Jan; 197(2):214-224. PubMed ID: 28930490 [TBL] [Abstract][Full Text] [Related]
12. 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. Davies JC; Sermet-Gaudelus I; Naehrlich L; Harris RS; Campbell D; Ahluwalia N; Short C; Haseltine E; Panorchan P; Saunders C; Owen CA; Wainwright CE; J Cyst Fibros; 2021 Jan; 20(1):68-77. PubMed ID: 32967799 [TBL] [Abstract][Full Text] [Related]
13. Disease burden in people with cystic fibrosis heterozygous for F508del and a minimal function mutation. Sawicki GS; Van Brunt K; Booth J; Bailey E; Millar SJ; Konstan MW; Flume PA J Cyst Fibros; 2022 Jan; 21(1):96-103. PubMed ID: 34289939 [TBL] [Abstract][Full Text] [Related]
14. The rescue of F508del-CFTR by elexacaftor/tezacaftor/ivacaftor (Trikafta) in human airway epithelial cells is underestimated due to the presence of ivacaftor. Becq F; Mirval S; Carrez T; Lévêque M; Billet A; Coraux C; Sage E; Cantereau A Eur Respir J; 2022 Feb; 59(2):. PubMed ID: 34266939 [TBL] [Abstract][Full Text] [Related]
15. Triple Therapy for Cystic Fibrosis Barry PJ; Mall MA; Álvarez A; Colombo C; de Winter-de Groot KM; Fajac I; McBennett KA; McKone EF; Ramsey BW; Sutharsan S; Taylor-Cousar JL; Tullis E; Ahluwalia N; Jun LS; Moskowitz SM; Prieto-Centurion V; Tian S; Waltz D; Xuan F; Zhang Y; Rowe SM; Polineni D; N Engl J Med; 2021 Aug; 385(9):815-825. PubMed ID: 34437784 [TBL] [Abstract][Full Text] [Related]
16. The expanded French compassionate programme for elexacaftor-tezacaftor-ivacaftor use in people with cystic fibrosis without a F508del CFTR variant: a real-world study. Burgel PR; Sermet-Gaudelus I; Girodon E; Durieu I; Houdouin V; Audousset C; Macey J; Grenet D; Porzio M; Murris-Espin M; Reix P; Baravalle M; Belleguic C; Mely L; Verhille J; Weiss L; Reynaud-Gaubert M; Mittaine M; Hamidfar R; Ramel S; Cosson L; Douvry B; Danner-Boucher I; Foucaud P; Roy C; Burnet E; Raynal C; Audrezet MP; Da Silva J; Martin C; Lancet Respir Med; 2024 Nov; 12(11):888-900. PubMed ID: 39151434 [TBL] [Abstract][Full Text] [Related]
17. Treatment effects of Elexacaftor/Tezacaftor/Ivacaftor in people with CF carrying non-F508del mutations. Livnat G; Dagan A; Heching M; Shmueli E; Prais D; Yaacoby-Bianu K; Stein N; Mei-Zahav M; Gur M; Cohen-Cymberknoh M; Shteinberg M J Cyst Fibros; 2023 May; 22(3):450-455. PubMed ID: 36372699 [TBL] [Abstract][Full Text] [Related]
19. A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One Zemanick ET; Taylor-Cousar JL; Davies J; Gibson RL; Mall MA; McKone EF; McNally P; Ramsey BW; Rayment JH; Rowe SM; Tullis E; Ahluwalia N; Chu C; Ho T; Moskowitz SM; Noel S; Tian S; Waltz D; Weinstock TG; Xuan F; Wainwright CE; McColley SA Am J Respir Crit Care Med; 2021 Jun; 203(12):1522-1532. PubMed ID: 33734030 [No Abstract] [Full Text] [Related]
20. Elexacaftor/Ivacaftor/Tezacaftor: First Approval. Hoy SM Drugs; 2019 Dec; 79(18):2001-2007. PubMed ID: 31784874 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]