CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 80 enrolled
Drug / intervention
BI 3006337 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05076422
NCT05076422Phase 1Completed

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

Boehringer Ingelheim·interventional·Posted Oct 13, 2021·Updated Jan 8, 2026

In Brief

A Phase 1 clinical trial evaluating BI 3006337 and Placebo for Healthy. Completed, enrolled 80 participants across 2 sites in 2 countries.

Detailed Summary

The main objectives of this trial are to investigate safety, tolerability and pharmacokinetics of BI 3006337 in healthy male subjects following subcutaneous administration of single-rising doses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesBelgium, Netherlands
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedOct 13, 2021
Enrollment StartOct 18, 2021
Primary CompletionMar 3, 2023
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 4.7 years ago

Interventions

BI 3006337drug

BI 3006337

Placebodrug

Placebo