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NCT04903509

A Study in Men With Overweight to Test How Well Different Doses of BI 1820237 Are Tolerated When Given as an Injection Alone or in Combination With Liraglutide

Completed Phase 1 Last updated 31 August 2022
What this trial tests

Phase 1 trial testing BI 1820237 in Healthy in 95 participants. Completed in 26 August 2022.

Timeline
8 June 2021
Primary endpoint
26 August 2022
26 August 2022

Quick facts

Lead sponsorBoehringer Ingelheim
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment95
Start date8 June 2021
Primary completion26 August 2022
Estimated completion26 August 2022
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Boehringer Ingelheim — full company profile →

Who can join

Adults 18 to 50, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main objective of this trial is to investigate safety, tolerability and pharmacokinetics (PK) and pharmacodynamics (PD) of BI 1820237 alone or together with a single low dose of liraglutide in male subjects with overweight/obesity (otherwise healthy) following subcutaneous administration of single rising doses.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A randomized phase I study of BI 1820237, a novel neuropeptide Y receptor type 2 agonist, alone or in combination with low-dose liraglutide in otherwise healthy men with overweight or obesity.
    Beetz N, Kalsch B, Forst T, Schmid B, et al · · 2025 · cited 8× · PMID 39373311 · DOI 10.1111/dom.15984

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Other trials of BI 1820237

Trials testing the same drug.

Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Boehringer Ingelheim trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04903509.

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