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

NCT06572111 | Terminated Phase 1

• 3 other identifiers: 1490-00062024-510870-26-00U1111-1308-5227
• Study Type: interventional
• Target: 8
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Healthy

Outcome Measures

Primary Outcomes (2)

• Mass balance and total recovery of [C-14]-radioactivity in urine and feces.

  Part A

  From drug administration up to Day 21.

• Area under the concentration-time curve of Carbon-14-labeled BI 1839100 after intravenous administration and BI 1839100 after oral administration, extrapolated to infinity (AUC0-∞).

  Part B

  From drug administration up to Day 21.

Secondary Outcomes (4)

• Maximum measured concentration of BI 1839100 and Carbon-14-labeled BI 1839100 in plasma (Cmax).

  Two hours before drug administration up to Day 21.

• Area under the concentration-time curve of BI 1839100 and Carbon-14-labeled BI 1839100 from 0 to the last quantifiable time point (AUC0-tz).

  Two hours before drug administration up to Day 21.

• Area under the concentration-time curve of Carbon-14-labeled BI 1839100 in plasma after intravenous administration and BI 1839100 after oral administration, from 0 to the last quantifiable time point (AUC0-tz).

  Two hours before drug administration up to 72 hours (Day 4).

• Maximum measured concentration of Carbon-14-labeled BI 1839100 in plasma after intravenous administration and BI 1839100 after oral administration (Cmax).

  Two hours before drug administration up to 72 hours (Day 4).

Study Arms (2)

Part A: BI 1839100 (C-14) formulation 1

EXPERIMENTAL

BI 1839100 (C-14) = BI 1839100 Carbon 14 Radiolabelled

Drug: BI 1839100 (C-14) formulation 1

Part B: BI 1839100 followed by BI 1839100 (C-14) formulation 2

EXPERIMENTAL

Drug: BI 1839100; Drug: BI 1839100 (C-14) formulation 2

Interventions

BI 1839100 (C-14) formulation 1 DRUG

BI 1839100 (C-14) formulation 1

Part A: BI 1839100 (C-14) formulation 1

BI 1839100 DRUG

BI 1839100

Part B: BI 1839100 followed by BI 1839100 (C-14) formulation 2

BI 1839100 (C-14) formulation 2 DRUG

BI 1839100 (C-14) formulation 2

Part B: BI 1839100 followed by BI 1839100 (C-14) formulation 2

Eligibility Criteria

• Age: 18 Years - 59 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy male subjects according to the assessment of the investigator, as based on a complete medical history including a physical examination, vital signs (blood pressure (BP), pulse rate (PR)), 12-lead electronic cardiogram (ECG), and clinical laboratory tests.
• Age of 18 to 59 years (inclusive at screening)
• Body mass index (BMI) of 18.5 to 30.0 kg/m2 (inclusive at screening)
• Signed and dated written informed consent in accordance with ICH-GCP and local legislation prior to admission to the trial

You may not qualify if:

• Any finding in the medical examination (including blood pressure (BP), pulse rate (PR), or ECG that deviates from normal and is assessed as clinically significant by the investigator
• Repeated measurement of systolic BP outside the range of 90 to 140 mmHg, diastolic BP outside the range of 50 to 90 mmHg, or PR outside the range of 45 to 90 bpm (subjects with PR values between 45 and 50 bpm may only be enrolled in case they have normal thyroid function (thyroid-stimulating hormone (TSH) and free thyroxine (FT4) at baseline-screening, no clinical symptoms associated with the bradycardia and no apparent signs of other diseases causing bradycardia such as hypothyroidism or heart conduction abnormalities)
• Any laboratory value outside the reference range that the investigator considers to be of clinical significance
• Any evidence of a concomitant disease assessed as clinically significant by the investigator
• Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders assessed as clinically significant by the investigator
• Cholecystectomy or other surgery of the gastrointestinal tract that could interfere with the Pharmacokinetics (PKs) of the trial medication (except appendectomy or simple hernia repair)
• Diseases of the central nervous system (including but not limited to any kind of seizures or stroke), and other relevant neurological or psychiatric disorders assessed as clinically relevant by the investigator

Sponsors & Collaborators

• Boehringer Ingelheim: lead

Study Sites (1)

ICON-Groningen-62040

Groningen, 9728 NZ, Netherlands

Location

Related Links

• Related Info

MeSH Terms

Interventions

Carbon-14

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Part A: open-label, single arm, single-dose Part B: non-randomized, open-label, single-arm, single period, fixed sequence, crossover

Study Record Dates

• First Submitted: August 23, 2024
• First Posted: August 26, 2024
• Study Start: September 30, 2024
• Primary Completion: October 28, 2024
• Study Completion: September 2, 2025
• Last Updated: September 23, 2025

Record last verified: 2025-09

Data Sharing

• IPD Sharing: Will not share

Locations

NL (1)