Overview
No overview information available.
Indication
Investigated for use/treatment in HIV infection.
Associated Conditions
No associated conditions information available.
Research Report
Alovudine (DB06198): A Comprehensive Report on a Thymidine Analog Antiviral Agent
1. Introduction to Alovudine
Alovudine is a synthetic pyrimidine 2',3'-dideoxyribonucleoside, specifically an analog of the natural nucleoside thymidine.[1] Its primary investigation centered on its potential as an antiviral agent for the treatment of Human Immunodeficiency Virus (HIV) infection.[3] Despite demonstrating in vitro potency, particularly against certain drug-resistant HIV strains, the clinical development of Alovudine for HIV was ultimately discontinued. The cessation of its development was primarily attributed to a challenging toxicity profile observed during clinical trials and, in the later stages, a failure to meet predefined efficacy targets at doses considered tolerable.[4]
Throughout its research and development phases, Alovudine has been identified by several synonyms. These include 3'-deoxy-3'-fluorothymidine (commonly abbreviated as FLT), MIV-310 (a designation used notably during its development by Medivir), and CL 184,824.[1] A comprehensive understanding of these alternative names is essential for navigating the historical literature and tracking the compound's progression through different research and corporate entities.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2014/09/05 | Phase 2 | Completed | |||
2001/08/31 | Not Applicable | Completed | |||
2001/08/31 | Not Applicable | Completed | |||
2001/08/31 | Not Applicable | 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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