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A Randomized, Placebo-Controlled, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunologic Effects of BMS-986256, and a Relative Bioavailability Study in Healthy Participants

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Trial Profile

A Randomized, Placebo-Controlled, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunologic Effects of BMS-986256, and a Relative Bioavailability Study in Healthy Participants

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 05 Jan 2022

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At a glance

  • Drugs Afimetoran (Primary)
  • Indications Autoimmune disorders; Cutaneous lupus erythematosus; Systemic lupus erythematosus
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 09 Nov 2021 Results assessing the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of BMS-986256 in healthy volunteers (HV), presented at the ACR Convergence 2021.
    • 25 Nov 2019 Status changed from active, no longer recruiting to completed.
    • 23 Sep 2019 Planned End Date changed from 25 Jul 2019 to 7 Oct 2019.

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