drugset / Trial / NCT06572111

A Study in Healthy Men to Test How BI 1839100 is Taken up and Handled by the Body

NCT06572111 ↗

Phase 1 Terminated 8 enrolled Boehringer Ingelheim
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This trial is conducted in healthy male subjects to evaluate the drug BI 1839100. The trial has two main parts. Part A aims to understand how BI 1839100 is processed in the body after an oral dose. It measures the total recovery of the drug and its radioactive label in urine and feces. It also determines the concentrations in blood plasma and investigates the drug's metabolic pathways. Part B aims to compare the absolute bioavailability of BI 1839100 when administered orally and intravenously.

Timeline

Start
2024-09-30
Primary completion
2024-10-28
Completion
2025-09-02

Outcome

Outcome not reported

Stopped: “Company decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1839100 Unknown — Oral

Indications

No indication recorded.