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Pleconaril and ribavirin in new-onset type 1 diabetes: a phase 2 randomized trial

Krogvold, Lars; Mynarek, Ida Maria; Ponzi, Erica; Mørk, Freja Barrett; Hessel, Trine Witzner; Roald, Trine; Lindblom, Nina; Westman, Jacob; Barker, Peter; Hyöty, Heikki; Ludvigsson, Johnny; Hanssen, Kristian F.; Johannesen, Jesper; Dahl-Jørgensen, Knut (2023-11)

 
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s41591-023-02576-1.pdf (3.376Mt)
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Krogvold, Lars
Mynarek, Ida Maria
Ponzi, Erica
Mørk, Freja Barrett
Hessel, Trine Witzner
Roald, Trine
Lindblom, Nina
Westman, Jacob
Barker, Peter
Hyöty, Heikki
Ludvigsson, Johnny
Hanssen, Kristian F.
Johannesen, Jesper
Dahl-Jørgensen, Knut
11 / 2023

NATURE MEDICINE
doi:10.1038/s41591-023-02576-1
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-2023120410443

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Peer reviewed
Tiivistelmä
<p>Previous studies showed a low-grade enterovirus infection in the pancreatic islets of patients with newly diagnosed type 1 diabetes (T1D). In the Diabetes Virus Detection (DiViD) Intervention, a phase 2, placebo-controlled, randomized, parallel group, double-blind trial, 96 children and adolescents (aged 6–15 years) with new-onset T1D received antiviral treatment with pleconaril and ribavirin (n = 47) or placebo (n = 49) for 6 months, with the aim of preserving β cell function. The primary endpoint was the mean stimulated C-peptide area under the curve (AUC) 12 months after the initiation of treatment (less than 3 weeks after diagnosis) using a mixed linear model. The model used longitudinal log-transformed serum C-peptide AUCs at baseline, at 3 months, 6 months and 1 year. The primary endpoint was met with the serum C-peptide AUC being higher in the pleconaril and ribavirin treatment group compared to the placebo group at 12 months (average marginal effect = 0.057 in the linear mixed model; 95% confidence interval = 0.004–0.11, P = 0.037). The treatment was well tolerated. The results show that antiviral treatment may preserve residual insulin production in children and adolescent with new-onset T1D. This provides a rationale for further evaluating antiviral strategies in the prevention and treatment of T1D. European Union Drug Regulating Authorities Clinical Trials identifier: 2015-003350-41 .</p>
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  • TUNICRIS-julkaisut [20210]
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste
 

 

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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste