Overview
The glycine amide of 4-aminobenzoic acid. Its sodium salt is used as a diagnostic aid to measure effective renal plasma flow (ERPF) and excretory capacity. [PubChem]
Indication
Used to measure effective renal plasma flow (ERPF) and to determine the functional capacity of the tubular excretory mechanism.
Associated Conditions
No associated conditions information available.
Research Report
Aminohippuric Acid (DB00345): A Comprehensive Pharmacological and Clinical Monograph
Executive Summary
Aminohippuric acid, also known as para-aminohippuric acid (PAH), is a small molecule diagnostic agent that has served for decades as the clinical and physiological gold standard for the measurement of renal hemodynamics.[1] As a synthetic derivative of hippuric acid, formed from the amino acid glycine and para-aminobenzoic acid, it is not found endogenously in humans and must be administered intravenously for its diagnostic purposes.[1] The foundational principle of its utility lies in its unique and remarkably efficient handling by the kidneys. In a healthy individual, aminohippuric acid is almost completely extracted from the blood in a single transit through the renal circulation, a process achieved through a dual mechanism of glomerular filtration and highly active tubular secretion.[3]
This high renal extraction ratio, approximately 92%, allows its plasma clearance to be used as a precise and reliable measure of Effective Renal Plasma Flow (ERPF).[1] Furthermore, by infusing the drug to concentrations that saturate the renal transport machinery, it is possible to determine the maximal functional capacity of the tubular secretory mechanism (TmPAH), providing a quantitative index of functional proximal tubular mass.[3] Historically, its properties as a substrate for renal transporters were leveraged in a therapeutic context; during World War II, it was co-administered with penicillin to competitively inhibit the antibiotic's renal clearance, thereby prolonging its therapeutic effect.[1]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/04/13 | Phase 2 | Recruiting | |||
2024/10/30 | Phase 2 | Active, not recruiting | |||
2023/01/23 | N/A | Recruiting | University Hospital of North Norway | ||
2022/09/07 | N/A | ENROLLING_BY_INVITATION | |||
2022/08/19 | Phase 2 | Recruiting | |||
2022/04/11 | N/A | Recruiting | |||
2021/10/04 | Phase 1 | Recruiting | |||
2021/08/17 | N/A | Recruiting | |||
2020/12/02 | Phase 4 | Active, not recruiting | |||
2020/10/06 | Phase 3 | Completed | Acceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway, NJ USA |
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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AMINOHIPPURATE SODIUM INJ LIQ 20% | merck frosst canada & cie, merck frosst canada & co. | 00140287 | Liquid - Intravenous | 20 % | 12/31/1991 |
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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