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A Phase 1, Open-label, Single-dose Study in Healthy Adult Participants to Assess the Bioequivalence Between Immediate Release Tablets and Minitablets, and to Assess the Food and pH Effect on the Pharmacokinetics of Deucravacitinib (BMS-986165) Administered as Minitablets

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Trial Profile

A Phase 1, Open-label, Single-dose Study in Healthy Adult Participants to Assess the Bioequivalence Between Immediate Release Tablets and Minitablets, and to Assess the Food and pH Effect on the Pharmacokinetics of Deucravacitinib (BMS-986165) Administered as Minitablets

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 04 Mar 2025

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At a glance

  • Drugs Deucravacitinib (Primary) ; Deucravacitinib (Primary) ; Famotidine
  • Indications Alopecia areata; Crohn's disease; Cutaneous lupus erythematosus; Discoid lupus erythematosus; Erythrodermic psoriasis; Hidradenitis suppurativa; Lupus nephritis; Plaque psoriasis; Psoriasis; Psoriatic arthritis; Pustular psoriasis; Sjogren's syndrome; Systemic lupus erythematosus; Ulcerative colitis
  • Focus Pharmacokinetics
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 04 Mar 2025 New trial record

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