Hypertension
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Sign up freeTop drugs studied for this disease
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CLINICAL_TRIALS trial_result · 2024-05-02Clinical Trial Update: Using Night-time Blood Pressure to Treat Hypertension [NA]
A clinical trial conducted at the Chinese University of Hong Kong evaluating night-time blood pressure management as a treatment for hyperte…
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CLINICAL_TRIALS research · 2024-05-01Clinical Trial Update: Home Blood Pressure Variability and Its Link to Arteriosclerosis and Metabolic Dysfunction in Hypertensive Patients
A clinical trial investigating how home blood pressure variability relates to arteriosclerosis and metabolic dysfunction in hypertensive pat…
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FDA approval · 2024-04-30FDA Approved: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — Supplemental Application (Jubilant Cadista Pharmaceuticals Inc.)
FDA approves a supplemental application for Jubilant Cadista's generic Losartan potassium and hydrochlorothiazide product.
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FDA label_change · 2024-04-30FDA Approved: VALSARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Alembic Pharmaceuticals Limited)
The FDA approved a supplemental application for valsartan and hydrochlorothiazide by Alembic Pharmaceuticals Limited, resulting in updates t…
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FDA approval · 2024-04-30FDA Approved: HYDROCHLOROTHIAZIDE — Supplemental Application (Accord Healthcare Inc.)
The FDA approved a supplemental application for hydrochlorothiazide filed by Accord Healthcare Inc. under ANDA 202556. The document does not…
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FDA approval · 2024-04-30FDA Approved: VALSARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Zydus Lifesciences Limited)
The FDA approved a supplemental application for a valsartan and hydrochlorothiazide generic product from Zydus Lifesciences Limited.
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FDA approval · 2024-04-30FDA Approved: HYDROCHLOROTHIAZIDE — Supplemental Application (ScieGen Pharmaceuticals Inc)
The FDA approved a supplemental application for hydrochlorothiazide submitted by ScieGen Pharmaceuticals Inc., endorsing changes to the prod…
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CLINICAL_TRIALS trial_result · 2024-04-29Clinical Trial Update: Effect of Home-exercise Programs Versus Supervised Core Stability Exercises on Hypertensive Patient With Low Back Pain [NA]
The study comparing home-exercise programs versus supervised core stability exercises in hypertensive patients with low back pain has comple…
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CLINICAL_TRIALS trial_result · 2024-04-29Clinical Trial Update: Preventing Weight Gain and Controlling Blood Pressure During Smoking Cessation in Hypertensive Smokers [NA]
This clinical trial evaluated strategies to prevent weight gain and control blood pressure during smoking cessation in hypertensive smokers.…
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CLINICAL_TRIALS trial_result · 2024-04-29Clinical Trial Update: Telemedicine Management of Hypertension [NA]
This document reports the completion of a clinical trial evaluating telemedicine management for hypertension.
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CLINICAL_TRIALS research · 2024-04-26Clinical Trial Update: Genetics of Hypertension Associated Treatments (GenHAT)
GenHAT is a genetics-focused clinical trial examining how genetic variation influences responses to hypertension treatments; the study statu…
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CLINICAL_TRIALS research · 2024-04-25Clinical Trial Update: The African-PREDICT Study
The African-PREDICT study, sponsored by North-West University in South Africa, investigates cardiovascular diseases and hypertension with a …
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CLINICAL_TRIALS trial_result · 2024-04-23Clinical Trial Update: A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention [NA]
A completed clinical trial evaluating a nurse-led intervention to extend the HIV treatment cascade and support cardiovascular disease preven…
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FDA approval · 2024-04-23FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (FRESENIUS KABI USA, LLC)
FDA approved the original application for Verapamil hydrochloride as a generic drug, manufactured by Fresenius Kabi USA, LLC. Verapamil hydr…
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FDA approval · 2024-04-17FDA Approved: NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE — Original Application (WG Critical Care, LLC)
FDA approved the original ANDA for NICARDIPINE HYDROCHLORIDE IN SODIUM CHLORIDE, a generic intravenous formulation from WG Critical Care, LL…
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CLINICAL_TRIALS trial_result · 2024-04-17Clinical Trial Update: SPYRAL DYSTAL Renal Denervation Global Clinical Study [NA]
Clinical trial update for SPYRAL DYSTAL Renal Denervation study conducted by Medtronic Vascular; trial status completed with results posted …
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CLINICAL_TRIALS trial_result · 2024-04-16Clinical Trial Update: Vascular Benefits of Adding CarvedilolCR to Type2 Diabetic Patients on ACEI. [Phase 4]
Phase 4 trial investigating whether adding carvedilolCR to ACE inhibitors provides vascular benefits in patients with type 2 diabetes and hy…
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FDA approval · 2024-04-16FDA Approved: CARVEDILOL PHOSPHATE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for carvedilol phosphate from Sun Pharmaceutical, confirming approval of this generic salt formulati…
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CLINICAL_TRIALS research · 2024-04-12Clinical Trial Update: Understanding the Exercise-Hypertension Paradox [NA]
A completed clinical trial update examining the exercise-hypertension paradox, with results posted in 2024.
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FDA approval · 2024-04-11FDA Approved: VALSARTAN AND HYDROCHLOROTHIAZIDE — Supplemental Application (Mylan Pharmaceuticals Inc.)
FDA granted approval of a supplemental application for valsartan and hydrochlorothiazide by Mylan Pharmaceuticals, enabling its generic prod…
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CLINICAL_TRIALS research · 2024-04-09Clinical Trial Update: Supporting Self-Management of Healthy Behaviors in Chronic Kidney Disease [NA]
This ClinicalTrials.gov update notes the study is completed and results have been posted for a University of Pennsylvania trial evaluating s…
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CLINICAL_TRIALS trial_result · 2024-04-05Clinical Trial Update: A Study to Evaluate the Efficacy and Safety of AD-209 [Phase 2]
Phase 2 clinical trial assessing efficacy and safety of AD-209 for hypertension (essential hypertension) has completed.
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FDA approval · 2024-04-04FDA Approved: HYDROCHLOROTHIAZIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Hydrochlorothiazide from Aurobindo Pharma Limited (generic).
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FDA approval · 2024-04-02FDA Approved: BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE — Supplemental Application (GLENMARK PHARMACEUTICALS INC., USA)
FDA approved a supplemental application for a generic fixed-dose combination of bisoprolol fumarate and hydrochlorothiazide for hypertension…
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FDA approval · 2024-04-02FDA Approved: FUROSEMIDE — Original Application (Devatis Inc.)
FDA approved Devatis Inc.'s original application for a generic furosemide product, enabling its marketing in the United States.