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Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Rising Subcutaneous Doses and Multiple Subcutaneous Doses Over 6 Weeks of BI 3006337 in Healthy Male Japanese Subjects (Single-blind, Randomised Within Dose Groups, Placebo-controlled, Parallel Group Design)

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Trial Profile

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Rising Subcutaneous Doses and Multiple Subcutaneous Doses Over 6 Weeks of BI 3006337 in Healthy Male Japanese Subjects (Single-blind, Randomised Within Dose Groups, Placebo-controlled, Parallel Group Design)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 28 Jan 2025

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At a glance

  • Drugs BI 3006337 (Primary)
  • Indications Non-alcoholic fatty liver disease; Obesity
  • Focus Adverse reactions
  • Sponsors Boehringer Ingelheim

Most Recent Events

  • 06 Nov 2024 Status changed from active, no longer recruiting to completed.
  • 29 Aug 2024 Status changed from recruiting to active, no longer recruiting.
  • 05 Apr 2024 Status changed from not yet recruiting to recruiting.

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