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Study of the Safety, Tolerability and Pharmacokinetics of LY3016859 After Single Intravenous and Subcutaneous Dosing in Healthy Volunteers

Trial Profile

Study of the Safety, Tolerability and Pharmacokinetics of LY3016859 After Single Intravenous and Subcutaneous Dosing in Healthy Volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Fepixnebart (Primary) ; Fepixnebart (Primary)
  • Indications Diabetic nephropathies
  • Focus Adverse reactions
  • Sponsors Eli Lilly and Company

Most Recent Events

  • 01 Jan 2018 Results from two initial early-phase clinical studies(TGAA; NCT01545583 and TGAB; NCT01774981), published in the Clinical Pharmacology in Drug Development Journal.
  • 13 Jun 2014 New trial record

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