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Safety of Eluxadoline in Patients with Irritable Bowel Syndrome with Diarrhea.
Cash, Brooks D; Lacy, Brian E; Schoenfeld, Philip S; Dove, Leonard S; Covington, Paul S.
Afiliação
  • Cash BD; Department of Medicine, University of South Alabama, Mobile, Alabama, USA.
  • Lacy BE; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Schoenfeld PS; University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
  • Dove LS; Furiex Pharmaceuticals, Inc., an affiliate of Allergan plc, Parsippany, New Jersey, USA.
  • Covington PS; Furiex Pharmaceuticals, Inc., an affiliate of Allergan plc, Parsippany, New Jersey, USA.
Am J Gastroenterol ; 112(2): 365-374, 2017 02.
Article em En | MEDLINE | ID: mdl-27922029
ABSTRACT

OBJECTIVES:

Eluxadoline is a mixed µ-opioid receptor (OR) and κ-OR agonist and δ-OR antagonist, approved for the treatment of irritable bowel syndrome with diarrhea (IBS-D). This analysis evaluated the safety and tolerability of eluxadoline 75 and 100 mg twice daily (BID) in one Phase 2 (IBS-2001) and two Phase 3 (IBS-3001 and IBS-3002) studies.

METHODS:

Adults with IBS-D (Rome III criteria) were randomized to placebo or eluxadoline (75 or 100 mg) BID for 12 (IBS-2001), 26 (IBS-3002), or 52 (IBS-3001) weeks. Safety data were pooled. Adverse events (AEs) were assessed, with special focus on opioid-related AEs, including suspected sphincter of Oddi spasm (SOS) events.

RESULTS:

2,776 patients were included in the enrolled set; the safety set comprised 2,814 patients, based on actual treatments received. The most frequent AEs in the placebo and eluxadoline 75 and 100 mg groups were constipation (2.5, 7.4, and 8.1%, respectively) and nausea (5.0, 8.1, and 7.1%, respectively); discontinuation due to constipation was uncommon (0.3, 1.1, and 1.5%, respectively). Ten SOS events (10/1,839; 0.5%) occurred in eluxadoline-treated patients, manifesting as acute abdominal pain with elevated aminotransferases or lipase, or pancreatitis; all occurred in patients without a gallbladder. Eight of these events occurred with the higher dose of eluxadoline, within 1 week of initiation of therapy, and all resolved with eluxadoline discontinuation. There were five events independently adjudicated as pancreatitis not associated with SOS, three of which were associated with heavy alcohol use.

CONCLUSIONS:

Eluxadoline was well tolerated in Phase 2 and 3 trials, with constipation and nausea the most common AEs. Consistent with the known adverse effects of opioid agonists, clinically apparent SOS events were observed in eluxadoline-treated patients. All occurred in patients without a gallbladder and the majority were observed in patients on the higher dose of eluxadoline, suggesting a possible association.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenilalanina / Espasmo / Fármacos Gastrointestinais / Constipação Intestinal / Síndrome do Intestino Irritável / Disfunção do Esfíncter da Ampola Hepatopancreática / Diarreia / Imidazóis / Náusea Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenilalanina / Espasmo / Fármacos Gastrointestinais / Constipação Intestinal / Síndrome do Intestino Irritável / Disfunção do Esfíncter da Ampola Hepatopancreática / Diarreia / Imidazóis / Náusea Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article