Overview
No overview information available.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
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
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/06/03 | Phase 1 | Not yet recruiting | |||
2025/04/08 | Phase 1 | Recruiting | |||
2024/02/13 | Phase 1 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
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No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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