Overview
The most significant modifiable risk factor for cardiovascular disease and the most prominent contributor to all-cause mortality is hypertension. Characterized by an office blood pressure of ≥140/90, hypertension is pervasive and impacts an estimated 25% of adults globally. Treatment for hypertension should include a number of lifestyle changes (ie. reduced sodium intake) along with pharmacotherapy - it should be noted that treatment with several antihypertensive agents may be required in order to achieve blood pressure targets. Thiazide-like diuretics such as indapamide are a valuable tool for the treatment of hypertension and continue to grow in popularity, falling behind only ACE inhibitors in terms of prescription frequency. When compared to hydrochlorothiazide (another commonly prescribed diuretic), indapamide has been shown to be superior at lowering systolic blood pressure, reducing left ventricular mass index, lowering oxidative stress, inhibiting platelet aggregation, and reducing microalbuminuria associated with diabetes. Interestingly, unlike thiazide diuretics, several sources suggest that indapamide is not associated with glucose or lipid disturbances. Indapamide is characterized by both a methylindoline and a sulfamoyl chlorobenzamide functional group, with the former being largely responsible for the molecule’s lipid solubility.
Background
The most significant modifiable risk factor for cardiovascular disease and the most prominent contributor to all-cause mortality is hypertension. Characterized by an office blood pressure of ≥140/90, hypertension is pervasive and impacts an estimated 25% of adults globally. Treatment for hypertension should include a number of lifestyle changes (ie. reduced sodium intake) along with pharmacotherapy - it should be noted that treatment with several antihypertensive agents may be required in order to achieve blood pressure targets. Thiazide-like diuretics such as indapamide are a valuable tool for the treatment of hypertension and continue to grow in popularity, falling behind only ACE inhibitors in terms of prescription frequency. When compared to hydrochlorothiazide (another commonly prescribed diuretic), indapamide has been shown to be superior at lowering systolic blood pressure, reducing left ventricular mass index, lowering oxidative stress, inhibiting platelet aggregation, and reducing microalbuminuria associated with diabetes. Interestingly, unlike thiazide diuretics, several sources suggest that indapamide is not associated with glucose or lipid disturbances. Indapamide is characterized by both a methylindoline and a sulfamoyl chlorobenzamide functional group, with the former being largely responsible for the molecule’s lipid solubility.
Indication
Indapamide is a diuretic indicated for use as monotherapy or in combination with other blood pressure-lowering agents to treat hypertension. It may also be used to treat fluid and salt retention associated with congestive heart failure.
Associated Conditions
- Hypertension
- Recurrent Nephrolithiasis
- Sodium and fluid retention
Research Report
Platelet-Rich Plasma: A Comprehensive Analysis of its Composition, Mechanisms, and Clinical Utility in Regenerative Medicine
I. Introduction to Platelet-Rich Plasma (PRP)
A. Definition and Core Concept
Platelet-Rich Plasma (PRP) is an autologous biological product derived from a patient's own whole blood. It represents a processed liquid fraction of peripheral blood characterized by a platelet concentration significantly above baseline physiological levels.[1] Normal human blood typically contains approximately 150,000 to 350,000 platelets per microliter. In contrast, therapeutic PRP preparations are generally designed to achieve platelet concentrations that are 3 to 5 times higher than this baseline, often aiming for or exceeding 1 million platelets per microliter.[3] Some advanced preparation systems report the capability to achieve even greater concentration factors, potentially up to 9-fold or 11-fold increases.[3]
This concentration of platelets results in a product rich in a diverse array of growth factors, cytokines, chemokines, and other bioactive molecules. These components are integral to the body's natural processes of tissue repair and regeneration.[1] The fundamental therapeutic rationale for utilizing PRP is to leverage and amplify these endogenous healing mechanisms. By delivering a supraphysiological dose of these reparative biomolecules directly to a site of injury, chronic degeneration, or surgical intervention, PRP aims to accelerate and enhance the natural healing cascade, potentially leading to improved clinical outcomes.[1]
B. Historical Background and Evolution
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/06/24 | Phase 4 | Recruiting | Lars Rejnmark | ||
2024/07/15 | Phase 3 | Completed | |||
2023/11/01 | Phase 2 | Recruiting | |||
2022/03/24 | Phase 4 | UNKNOWN | |||
2022/03/21 | Phase 3 | Completed | |||
2021/11/02 | Phase 2 | Completed | |||
2021/08/19 | Phase 2 | Recruiting | |||
2020/07/02 | Phase 4 | UNKNOWN | Shanghai Jiao Tong University School of Medicine | ||
2019/01/23 | Phase 3 | Withdrawn | EMS | ||
2019/01/23 | Phase 3 | Withdrawn | EMS |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Actavis Pharma, Inc. | 0228-2571 | ORAL | 2.5 mg in 1 1 | 10/26/2023 | |
Rebel Distributors Corp | 21695-576 | ORAL | 1.25 mg in 1 1 | 11/28/2006 | |
ANI Pharmaceuticals, Inc. | 62559-510 | ORAL | 1.25 mg in 1 1 | 4/24/2017 | |
ANI Pharmaceuticals, Inc. | 62559-511 | ORAL | 2.5 mg in 1 1 | 4/24/2017 | |
Rising Pharma Holdings, Inc. | 16571-875 | ORAL | 1.25 mg in 1 1 | 6/26/2023 | |
Actavis Pharma, Inc. | 0228-2597 | ORAL | 1.25 mg in 1 1 | 10/26/2023 | |
Bryant Ranch Prepack | 71335-1541 | ORAL | 1.25 mg in 1 1 | 2/4/2022 | |
Bryant Ranch Prepack | 63629-1953 | ORAL | 1.25 mg in 1 1 | 4/24/2017 | |
Rising Pharma Holdings, Inc. | 16571-876 | ORAL | 2.5 mg in 1 1 | 6/26/2023 | |
Preferred Pharmaceuticals Inc. | 68788-7247 | ORAL | 2.5 mg in 1 1 | 7/13/2023 |
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 |
---|---|---|---|---|---|
RINALIX TABLET 2.5 mg | SIN11664P | TABLET, FILM COATED | 2.5 mg | 9/13/2001 | |
NATRIXAM MODIFIED RELEASE TABLET 1.5 mg/10 mg | SIN14902P | TABLET, MULTILAYER, EXTENDED RELEASE | 1.5 mg | 12/3/2015 | |
SWILIX SR TABLET 1.5MG | SIN16750P | TABLET, FILM COATED, EXTENDED RELEASE | 1.50mg | 3/30/2023 | |
APO-INDAPAMIDE TABLET 2.5 mg | SIN10161P | TABLET, FILM COATED | 2.5 mg | 10/5/1998 | |
NATRILIX SR TABLET 1.5 mg | SIN09074P | TABLET, FILM COATED | 1.5 mg | 12/14/1996 | |
COVERSYL PLUS TABLET 5mg/1.25mg | SIN13633P | TABLET, FILM COATED | 1.25mg | 4/24/2009 | |
TRIPLIXAM FILM COATED TABLET 10 mg/ 2.5 mg/ 5 mg | SIN15013P | TABLET, FILM COATED | 2.5 mg | 5/23/2016 | |
TRIPLIXAM FILM COATED TABLET 10 mg/ 2.5 mg/ 10 mg | SIN15014P | TABLET, FILM COATED | 2.5 mg | 5/23/2016 | |
TRIPLIXAM FILM COATED TABLET 5 mg/ 1.25 mg/ 5 mg | SIN15011P | TABLET, FILM COATED | 1.25 mg | 5/23/2016 | |
NATRIXAM MODIFIED RELEASE TABLET 1.5 mg/5 mg | SIN14901P | TABLET, MULTILAYER, EXTENDED RELEASE | 1.5 mg | 12/3/2015 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
Indapamide Sustained-release Capsules | 国药准字H20051554 | 化学药品 | 胶囊剂 | 8/29/2020 | |
Indapamide Sustained-release Capsules | 国药准字H20090010 | 化学药品 | 胶囊剂 | 8/23/2023 | |
Indapamide Sustained-release Capsules | 国药准字H20130090 | 化学药品 | 胶囊剂 | 12/20/2022 | |
Indapamide Sustained Release Tablets | 国药准字H20052001 | 化学药品 | 片剂 | 8/28/2020 | |
Indapamide Sustained Release Tablets | 国药准字H20244057 | 化学药品 | 片剂 | 6/18/2024 | |
Indapamide Sustained Release Tablets | 国药准字H20213537 | 化学药品 | 片剂 | 6/22/2021 | |
Indapamide Sustained Release Tablets | 国药准字H20253856 | 化学药品 | 片剂 | 4/8/2025 | |
Indapamide Sustained Release Tablets | 国药准字HJ20171296 | 化学药品 | 片剂 | 4/25/2023 | |
Indapamide Sustained Release Tablets | 国药准字H20031281 | 化学药品 | 片剂 | 12/4/2019 | |
Indapamide Sustained Release Tablets | 国药准字H20051896 | 化学药品 | 片剂 | 4/7/2020 |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
VICK-TRILIX TAB 2.5MG | N/A | vickmans laboratories ltd | N/A | N/A | 3/6/2006 |
MOREEZ COMPLEX TABLETS | N/A | wilcome pharmaceutical co ltd | N/A | N/A | 5/24/2018 |
INDAPIN SR FILM-COATED TAB 1.5MG | N/A | wilcome pharmaceutical co ltd | N/A | N/A | 7/28/2009 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Indapamide 2.5 mg tablet bottle | 481776 | Medicine | A | 3/5/2025 | |
Indapamide 1.25 mg tablet bottle | 481775 | Medicine | A | 3/5/2025 |