Budesonide Orodispersible Tablets Maintain Remission in a Randomized, Placebo-Controlled Trial of Patients With Eosinophilic Esophagitis.

Details

Serval ID
serval:BIB_2C0D0D781E8F
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Budesonide Orodispersible Tablets Maintain Remission in a Randomized, Placebo-Controlled Trial of Patients With Eosinophilic Esophagitis.
Journal
Gastroenterology
Author(s)
Straumann A., Lucendo A.J., Miehlke S., Vieth M., Schlag C., Biedermann L., Vaquero C.S., Ciriza de Los Rios C., Schmoecker C., Madisch A., Hruz P., Hayat J., von Arnim U., Bredenoord A.J., Schubert S., Mueller R., Greinwald R., Schoepfer A., Attwood S.
Working group(s)
International EOS-2 Study Group
Contributor(s)
Tack J., Miehlke S., Bajbouj M., Brückner S., Fibbe C., Haag S., Schmöcker C., Hartmann D., Lammert F., Madisch A., Reinshagen M., Schubert S., von Arnim U., Börner N., Witzemann D., Caca K., Albert J., Zeuzem S., Wiedbrauck F., Messmann H., Bredenoord A.J., Verdonk R., Wolfhagen F., Villarin A.L., Vaquero C.S., de Los Ríos C.C., Juan A.P., Martinez I.P., Sanchez-Migallon J.R., Andrés J.B., Aisa Á., Straumann A., Hruz P., Schoepfer A., Biedermann L., Hayat J., Dhar A.
ISSN
1528-0012 (Electronic)
ISSN-L
0016-5085
Publication state
Published
Issued date
11/2020
Peer-reviewed
Oui
Volume
159
Number
5
Pages
1672-1685.e5
Language
english
Notes
Publication types: Clinical Trial, Phase III ; Comparative Study ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder. Swallowed topical-acting corticosteroids are effective in bringing active EoE into remission. However, it is not clear whether these drugs are effective for long-term maintenance of remission.
We performed a double-blind trial to compare the efficacy and safety of 2 dosages of a budesonide orodispersible tablet (BOT) vs placebo in maintaining remission of EoE. Maintenance of remission was defined as absence of clinical and histologic relapse and no premature withdrawal for any reason. Two hundred and four adults with EoE in clinical and histologic remission, from 29 European study sites, were randomly assigned to groups given BOT 0.5 mg twice daily (n = 68), BOT 1.0 mg twice daily (n = 68), or placebo twice daily (n = 68) for up to 48 weeks.
At end of treatment, 73.5% of patients receiving BOT 0.5 mg twice daily and 75% receiving BOT 1.0 mg twice daily were in persistent remission compared with 4.4% of patients in the placebo group (P < .001 for both comparisons of BOT with placebo). Median time to relapse in the placebo group was 87 days. The frequency of adverse events was similar in the BOT and placebo groups. Morning serum levels of cortisol were in the normal range at baseline and did not significantly change during treatment. Four patients receiving BOT developed asymptomatic, low serum levels of cortisol. Clinically manifested candidiasis was suspected in 16.2% of patients in the BOT 0.5 mg group and in 11.8% of patients in the BOT 1.0 mg group; all infections resolved with treatment.
In a phase 3 trial, up to 48 weeks of treatment with BOT (0.5 mg or 1.0 mg twice daily) was superior to placebo in maintaining remission of EoE. Both dosages were equally effective and well tolerated. EudraCT number; 2014-001485-99; ClinicalTrials.gov number, NCT02434029.
Keywords
Administration, Oral, Adrenal Cortex Hormones/administration & dosage, Adrenal Cortex Hormones/adverse effects, Adult, Budesonide/administration & dosage, Budesonide/adverse effects, Double-Blind Method, Eosinophilic Esophagitis/diagnosis, Eosinophilic Esophagitis/drug therapy, Europe, Female, Humans, Male, Middle Aged, Remission Induction, Tablets, Time Factors, Treatment Outcome, Dysphagia, Patient-Reported Outcomes, Remission, Topical Corticosteroids
Pubmed
Web of science
Open Access
Yes
Create date
13/08/2020 9:43
Last modification date
16/04/2024 7:12
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