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Concomitant Administration of Ozanimod and Serotonergic Antidepressants in Patients With Ulcerative Colitis or Relapsing Multiple Sclerosis.
Regueiro, Miguel; Siegmund, Britta; Horst, Sara; Moslin, Ryan; Charles, Lorna; Petersen, AnnKatrin; Tatosian, Daniel; Wu, Hsiuanlin; Lawlor, Garrett; Fischer, Monika; D'Haens, Geert; Colombel, Jean-Frederic.
Afiliação
  • Regueiro M; Cleveland Clinic, Cleveland, OH, USA.
  • Siegmund B; Department of Gastroenterology, Infectious Diseases, and Rheumatology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
  • Horst S; Vanderbilt University Medical Center, Nashville, TN, USA.
  • Moslin R; Bristol Myers Squibb, Princeton, NJ, USA.
  • Charles L; Bristol Myers Squibb, Princeton, NJ, USA.
  • Petersen A; Bristol Myers Squibb, Princeton, NJ, USA.
  • Tatosian D; Bristol Myers Squibb, Princeton, NJ, USA.
  • Wu H; Bristol Myers Squibb, Princeton, NJ, USA.
  • Lawlor G; Bristol Myers Squibb, Princeton, NJ, USA.
  • Fischer M; Indiana University School of Medicine, Indianapolis, IN, USA.
  • D'Haens G; Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • Colombel JF; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Inflamm Bowel Dis ; 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-39018016
ABSTRACT

BACKGROUND:

Ozanimod, approved for the treatment of moderately to severely active ulcerative colitis (UC) and relapsing multiple sclerosis (RMS), is a weak in vitro monoamine oxidase B (MAO-B) inhibitor. MAO-B inhibitors can cause serotonin accumulation with concomitant use of selective serotonin reuptake inhibitors (SSRIs) or serotonin and norepinephrine reuptake inhibitors (SNRIs). We evaluated the incidence of treatment-emergent adverse events (TEAEs) potentially associated with serotonin accumulation during ozanimod and concomitant SSRI/SNRI use in this post hoc analysis of pooled UC studies and the open-label extension RMS DAYBREAK.

METHODS:

Data for ozanimod 0.92 mg from pooled UC studies (n = 1158; cutoff January 10, 2022) and RMS DAYBREAK (n = 2257; cutoff February 1, 2022) were analyzed. Concomitant SSRI/SNRI use was allowed in the UC (n = 67) and RMS (n = 274) studies. A narrow Medical Dictionary for Regulatory Activities search ("serotonin syndrome," "neuroleptic malignant syndrome," and "malignant hyperthermia") and a broad search including terms potentially associated with serotonin accumulation were conducted. The percentages of patients with TEAEs in both searches were analyzed by concomitant SSRI/SNRI use when the TEAE occurred.

RESULTS:

No patients had TEAEs matching the narrow search criteria. No differences were observed in the percentages of patients with ≥1 TEAE matching the broad search regardless of SSRI/SNRI use in UC (with 25.4% [n = 17 of 67]; without 15.0% [n = 164 of 1091]) and RMS (with 12.4% [n = 34 of 274]; without 15.6% [n = 310 of 1982]) studies.

CONCLUSIONS:

No evidence of increased TEAEs potentially associated with serotonin accumulation was observed with concurrent use of ozanimod and SSRIs/SNRIs. CLINICAL TRIAL REGISTRATION NCT01647516, NCT02531126, NCT02435992, NCT02576717.
No evidence of increased treatment-emergent adverse effects potentially associated with serotonin accumulation was observed with concurrent use of ozanimod and serotonergic antidepressants. Our findings support the absence of clinically meaningful ozanimod monoamine oxidase B inhibition in vivo.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article