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Neil Ahluwalia

Vertex Pharmaceuticals
H指数:25
被引数:4,129

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Effects of Elexacaftor/Tezacaftor/Ivacaftor on cough frequency, physical activity patterns, and sleep quality in adolescents and adults with cystic fibrosis

Elexacaftor/Tezacaftor/Ivacaftor对囊性纤维化青少年和成人患者咳嗽频率、身体活动模式及睡眠质量的影响

2026-03-310
OAAI
Long-term safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis and at least one F508del allele: 144-week interim results from a 192-week open-label extension study
2023-11-0921
OAAI
Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged ≥6 Years with Cystic Fibrosis and at Least One F508del Allele A Phase 3, Open-Label Clinical Trial
2023-07-0122
OA
Phase 3 Open-Label Clinical Trial of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged 2-5 Years with Cystic Fibrosis and at Least One F508del Allele
2023-07-0150
OAAI
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for F508del and a Minimal Function Mutation A Phase 3b, Randomized, Placebo-controlled Study
2022-12-0162
OAAI
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
2022-07-018
OAAI
Triple Therapy for Cystic Fibrosis Phe508del-Gating and -Residual Function Genotypes
2021-08-26168
OA
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study
2021-07-0136
OAAI
A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/lvacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele
2021-06-15156
OAAI
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
2021-01-0147
OAAI
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
LANCET
IF88.5
2019-11-01858
OAAI
ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosis (vol 23, pg 1405, 2017)
2017-12-014
OAAI
ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosis
2017-10-23109
OAAI