Overview
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Indication
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Associated Conditions
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Research Report
Comprehensive Report on the Investigational Compound LY3872386
I. Executive Summary
LY3872386 was an investigational small molecule compound developed by Eli Lilly and Company, primarily targeting atopic dermatitis. Classified therapeutically as an anti-inflammatory agent for skin disorders, its specific mechanism of action remained undefined throughout its development.1 The compound advanced to Phase 1 clinical evaluation in a multicenter, multifaceted study (NCT06119529) designed to assess its safety, tolerability, and pharmacokinetics in both healthy volunteers and patients with atopic dermatitis.2 However, clinical development was abruptly terminated in July 2024, reportedly due to "emerging nonclinical data".1 This early-stage termination, occurring relatively shortly after trial initiation, suggests the discovery of a significant safety or developability concern in concurrent or newly reviewed nonclinical studies, leading to a swift cessation of human investigation.
II. Introduction to LY3872386
A. Compound Identification and Originator
The investigational drug LY3872386, also referred to as LY 3872386, was under development by Eli Lilly and Company.1 As a novel therapeutic candidate, it represented an effort by a major pharmaceutical entity to address unmet needs in dermatological conditions.
B. Pharmacological Classification
LY3872386 was identified as a small molecule drug.4 Its intended therapeutic applications placed it within the categories of "Anti-inflammatories" and "Skin disorder therapies".1 It was designated as a New Molecular Entity (NME), indicating a chemical structure not previously approved for therapeutic use.1 The compound did not hold Orphan Drug Status.1
C. Mechanism of Action
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/11/07 | Phase 1 | Terminated |
FDA Drug Approvals
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No FDA approvals found for this drug. |
EMA Drug Approvals
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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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