MedPath

BI-3031185

Generic Name
BI-3031185

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: May 15, 2025

Comprehensive Report on the Investigational Compound BI-3031185

1. Executive Summary

BI-3031185 is an orally administered small molecule investigational drug, classified as a New Molecular Entity (NME), currently under development by the global pharmaceutical company Boehringer Ingelheim. The compound is in the early stages of Phase 1 clinical development, with studies primarily focused on evaluating its safety, tolerability, and pharmacokinetic profile in healthy male volunteers. Completed and ongoing trials are assessing single ascending doses, multiple ascending doses, the influence of food on bioavailability, and potential drug-drug interactions, notably with Midazolam, a CYP3A4 probe substrate.

To date, the specific mechanism of action and the intended therapeutic target(s) for BI-3031185 have not been publicly disclosed by the developer. Preclinical development was reportedly completed in Germany prior to February 2024, enabling the transition to human trials. While associated patent information is indicated in some databases, specific details are not publicly available. The compound does not currently hold Orphan Drug Status. The successful outcome of the current Phase 1 program, particularly regarding safety and pharmacokinetic characterization, will be crucial in determining the future development pathway for BI-3031185, including its potential progression into patient-based studies and the eventual elucidation of its therapeutic utility.

2. Introduction to BI-3031185

Overview

Continue reading the full research report

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.