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Research Report
Zinlirvimab (10-1074-LS): A Comprehensive Analysis of a Long-Acting Broadly Neutralizing Antibody for HIV Treatment and Prevention
Section 1: Executive Summary & Overview of Zinlirvimab (10-1074-LS)
Introduction and Nomenclature
10-1074-LS is an investigational human monoclonal antibody being developed for the treatment and prevention of Human Immunodeficiency Virus Type 1 (HIV-1) infection. It represents a significant advancement in the field of passive immunotherapy, belonging to a class of molecules known as broadly neutralizing antibodies (bNAbs).[1] Originally discovered by researchers at The Rockefeller University, the antibody and its long-acting variant have been licensed for clinical development by Gilead Sciences, Inc..[3] In this context, it is identified by several names: the research designation 10-1074-LS, the generic name zinlirvimab, and the Gilead development code GS-2872.[2] The "-LS" suffix denotes a critical modification engineered to extend its biological half-life, a feature central to its therapeutic strategy.
Classification and Therapeutic Rationale
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/11/07 | Phase 1 | Recruiting | Shandong Suncadia Medicine Co., Ltd. | ||
2023/03/23 | Phase 1 | Not yet recruiting |
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
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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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