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Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Different Titration Schedules of Subcutaneous Doses of BI 1820237 Alone or Together With Either Semaglutide or BI 456906 in Otherwise Healthy Male and Female Individuals With Obesity/Overweight (Multiple Dose, Single-blind, Randomised, Placebo-controlled, Parallel Group Design)

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Trial Profile

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Different Titration Schedules of Subcutaneous Doses of BI 1820237 Alone or Together With Either Semaglutide or BI 456906 in Otherwise Healthy Male and Female Individuals With Obesity/Overweight (Multiple Dose, Single-blind, Randomised, Placebo-controlled, Parallel Group Design)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 19 Nov 2024

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At a glance

  • Drugs BI 1820237 (Primary) ; Survodutide (Primary) ; Semaglutide
  • Indications Obesity
  • Focus Adverse reactions
  • Sponsors Boehringer Ingelheim

Most Recent Events

  • 06 Aug 2024 Status changed from active, no longer recruiting to completed.
  • 23 Feb 2024 Status changed from recruiting to active, no longer recruiting.
  • 15 Jan 2024 Planned End Date changed from 25 Apr 2024 to 31 Jul 2024.

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