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Research Report
An Overview of the Investigational HIV-1 Maturation Inhibitor GSK3739937 (VH3739937)
I. Introduction to GSK3739937
A. Overview of GSK3739937 (VH3739937)
GSK3739937, also identified in scientific literature and development programs as VH3739937 or by the internal research code VH-937, is an investigational small molecule compound.[1] It has been developed primarily for its potential therapeutic application in the management of Human Immunodeficiency Virus Type 1 (HIV-1) infection.[1] The compound is structurally related to GSK3640254, an earlier-generation HIV-1 maturation inhibitor.[5] The consistent use of dual nomenclature, GSK3739937 and VH3739937, across research publications and trial registries is noteworthy, with "VH" likely indicating the involvement of ViiV Healthcare in its development. This is a common practice in pharmaceutical development where internal research codes (e.g., VH-937) and corporate identifiers (e.g., GSK3739937) may be used concurrently. Clarification of this nomenclature is important for accurately tracking the compound's progress through various stages of research and development.
B. Chemical Nature and Drug Class (HIV-1 Maturation Inhibitor)
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/09/29 | Phase 2 | Terminated |
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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