Drugs / ELX/TEZ/IVA
last change Sep 2025 re-read 3 minutes ago

ELX/TEZ/IVA

Developed for
cystic fibrosis
Investigated by
Vertex Pharmaceuticals Incorporated

Trials 1

202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 3 NCT05882357 Jun 2023 → Sep 2025 cystic fibrosis Vertex Pharmaceuticals Incorporated Completed No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2024-06-07 Vertex Pharmaceuticals Incorporated Results Vertex Presents New Data at the European Cystic Fibrosis Conference Demonstrating Significant Benefits of Treatment with TRIKAFTA® vrtx.com ↗
Data from a randomized, double-blind, Phase 3 study (abstract WS06.04) demonstrated that people with CF who have rare, non-F508del mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene responsive to TRIKAFTA® in vitro demonstrated clinical benefit from receiving TRIKAFTA®.
2023-06-09 Vertex Pharmaceuticals Incorporated Results Vertex Presents Data Demonstrating Significant Benefits of Long-Term Treatment With CFTR Modulators at the European Cystic Fibrosis Conference vrtx.com ↗
The data on TRIKAFTA in particular demonstrate that this medicine improves lung function sustainably and in a real-world setting.
2019-10-31 Vertex Pharmaceuticals Incorporated Results Phase 3 Results from Two Studies of TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) Triple Combination Treatment for Cystic Fibrosis Concurrently Published in The New England Journal of Medicine and The Lancet vrtx.com ↗
Both studies met primary and all key secondary endpoints, demonstrating statistically significant and clinically meaningful improvements in lung function and other measures of disease.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as ELX/TEZ/IVA ClinicalTrials.gov intervention name — accepted as the source's own label NCT05882357 ↗
Route Oral “Fixed-dose combination granules for oral administration.” NCT05882357 ↗