A functional comparison of readthrough agent ELX-02 across a wide range of nonsense CFTR variants.

Authors

Marlies Destoop, Anabela S Ramalho, Iris A L Silva, Annelotte M Vonk, Sylvia Suen, Marlou C Bierlaagh, Sylvia F Boj, Robert G J Vries, Jeffrey M Beekman, Kris De Boeck, Cornelis K van der Ent, Margarida D Amaral, Francois Vermeulen, Sacha Spelier, HIT-CF Organoid Study Group

Published in

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. Sep 11, 2026. Epub Sep 11, 2026.

Abstract

Nonsense variants in CFTR account for ∼10% of cystic fibrosis (CF) variants and cannot be treated with available CFTR modulators. Translational readthrough agents such as ELX-02 offer a potential therapeutic strategy for CFTR nonsense variants, but clinical trials, conducted primarily in individuals carrying the G542X variant, have demonstrated limited efficacy. Our study aimed to evaluate ELX-02-mediated CFTR rescue across a broad range of nonsense variants using patient-derived intestinal organoids (PDIOs) to define variant-specific determinants of readthrough efficacy and assess its potential across a genetically diverse CF population.
The ex vivo response to ELX-02 was assessed in 206 PDIOs carrying heterogeneous nonsense variants. CFTR function was quantified using the forskolin-induced swelling (FIS) assay after 48-hour exposure to ELX-02. Responses were analysed by genotype and stop codon identity, with secondary validation performed in a selected subset of PDIOs (n = 60).
ELX-02-mediated CFTR rescue varied markedly, ranging from responses approaching those observed with approved CFTR modulators (LUM/IVA) to responses at or below detection limit. Overall, maximal responses were modest and at the lower end of the functional range for CFTR modulators. Rescue was dose-dependent and higher in PDIOs carrying two nonsense variants when compared with PDIOs carrying a single nonsense variant combined with a residual or minimal function variant. Nonsense variants in nucleotide-binding domain 1, including G542X, S466X, G550X and R553X, showed relatively higher responsiveness.
ELX-02 induces limited and highly heterogeneous CFTR rescue across nonsense variants. PDIO-based functional screening provides a framework to guide patient selection and stratification for future readthrough therapy trials.

PMID:
42728176
Bibliographic data and abstract were imported from PubMed on 12 Sep 2026.

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