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Research Report
An In-Depth Analysis of the Investigational Compound GS-1720 and Clarification of the "GS-17" Designation
Executive Summary
This report provides a comprehensive analysis of the medication designated "GS-17," a query that encompasses multiple distinct pharmaceutical, supplemental, and investigational entities. Initial analysis reveals that the designation is ambiguous. The pill imprint "G 17" refers to at least two different commercially available medications: an over-the-counter analgesic and sleep aid combining diphenhydramine and naproxen sodium, and a prescription urinary tract analgesic, phenazopyridine hydrochloride. Furthermore, "GS 17 CAP" is the name of a multivitamin supplement produced in India. However, the most significant and data-rich subject associated with this nomenclature is the investigational compound GS-1720, a novel, long-acting oral antiretroviral for the treatment of HIV-1 infection developed by Gilead Sciences.
GS-1720 is an integrase strand transfer inhibitor (INSTI) designed for once-weekly administration, representing a potential paradigm shift from the current standard of daily oral therapy. Developed to be co-administered with GS-4182 (a prodrug of the capsid inhibitor lenacapavir), the combination regimen aims to address the unmet need for more convenient HIV treatment options, potentially improving long-term adherence and quality of life for people with HIV. Early-phase clinical trials demonstrated a promising profile for GS-1720, characterized by potent antiviral activity, a high barrier to resistance, a long pharmacokinetic half-life suitable for weekly dosing, and a favorable initial safety profile in both healthy volunteers and people with HIV.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2025/09/24 | Not Applicable | Not yet recruiting | |||
2025/06/26 | Phase 1 | Not yet recruiting | |||
2025/06/17 | Phase 2 | Not yet recruiting | |||
2024/09/19 | Phase 1 | Recruiting | |||
2024/06/03 | Phase 1 | Recruiting | |||
2024/02/28 | Phase 1 | Recruiting | |||
2023/08/07 | Phase 1 | Recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| No Health Canada approvals found for this drug. | |||||
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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