Vytorin

Coronary heart disease, prophylaxis of cardiovascular event, Diabetes + 11 more

Treatment

19 FDA approvals

20 Active Studies for Vytorin

What is Vytorin

Simvastatin

The Generic name of this drug

Treatment Summary

Ezetimibe is a medicine used to lower cholesterol levels. It works by blocking the absorption of cholesterol and phytosterols in the intestines. This drug was first studied in the 1990s and has been proven to be effective in treating high cholesterol levels due to primary hyperlipidemia, mixed hyperlipidemia, homozygous familial hypercholesterolemia, and homozygous sitosterolemia. Unlike other cholesterol-lowering drugs such as statins and bile acid sequestrants, Ezetimibe works by targeting a specific protein called Niemann-Pick C1-Like 1 (NPC1

Zocor

is the brand name

image of different drug pills on a surface

Vytorin Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Zocor

Simvastatin

1991

620

Approved as Treatment by the FDA

Simvastatin, otherwise called Zocor, is approved by the FDA for 19 uses like Diabetes Mellitus and Homozygous Familial Hypercholesterolemia .

Diabetes Mellitus

Homozygous Familial Hypercholesterolemia

Used to treat Homozygous Familial Hypercholesterolaemia (HoFH) in combination with Ezetimibe

Hypercholesterolemia

Used to treat Heterozygous Familial Hypercholesterolemia (HeFH) in combination with Ezetimibe

Mixed Hyperlipidemia

Used to treat Mixed Hyperlipidemia in combination with Ezetimibe

Diet

Used to treat Diet in combination with Ezetimibe

Lipid-Lowering Therapy

Used to treat Lipid-Lowering Therapy in combination with Ezetimibe

Homozygous Familial Hypercholesterolaemia (HoFH)

Used to treat Homozygous Familial Hypercholesterolaemia (HoFH) in combination with Ezetimibe

history of stroke or other cerebrovascular disease cardiovascular event

prophylaxis of cardiovascular event

Heterozygous Familial Hypercholesterolemia (HeFH)

Used to treat Heterozygous Familial Hypercholesterolemia (HeFH) in combination with Ezetimibe

Physical Activity

Used to treat Exercise in combination with Ezetimibe

history of coronary heart disease cardiovascular event

Cardiovascular Events

cholesterol

Helps manage High Cholesterol

Peripheral Vascular Disease Patient

Diabetes

Coronary heart disease

Peripheral Vascular Disease

Cerebrovascular Disorders

Effectiveness

How Vytorin Affects Patients

Ezetimibe helps lower cholesterol levels such as total cholesterol, low-density lipoprotein cholesterol, apoprotein B, non-high-density lipoprotein cholesterol and triglycerides, while increasing the level of high-density lipoprotein cholesterol. When taken in the recommended dose, it can reduce LDL levels by 15-20% and increase HDL-C by 2.5-5%. Those with moderate-severe liver impairment should avoid taking ezetimibe, and it is important to note that there have been reports of muscle pain and damage (rhabdomyolysis) in those taking ezetim

How Vytorin works in the body

Ezetimibe works to reduce cholesterol levels by blocking a protein in the intestine that helps absorb cholesterol. Ezetimibe attaches to the protein, called NPC1L1, and prevents it from pulling cholesterol into the cell. This reduces the amount of cholesterol that is absorbed by the intestine and sent to the liver, resulting in lower cholesterol levels in the body. It is not fully understood how Ezetimibe works, but one study suggests that it prevents the NPC1L1 protein from binding to cholesterol, while another suggests that it disrupts other proteins involved in cholesterol absorption.

When to interrupt dosage

The prescribed dosage of Vytorin is contingent upon the established condition, such as Diet, Homozygous Familial Hypercholesterolemia and Hyperlipidemia. The measure of dosage alters, as per the delivery approach (e.g. Oral or Tablet), outlined in the table below.

Condition

Dosage

Administration

Mixed Hyperlipidemia

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Peripheral Vascular Disease

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Coronary heart disease

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

prophylaxis of cardiovascular event

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Diabetes

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Cardiovascular Events

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Physical Activity

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Type 2 Diabetes

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

cholesterol

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Diet

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Lipid-Lowering Therapy

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Hypercholesterolemia

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Cerebrovascular Disorders

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Homozygous Familial Hypercholesterolemia

, 80.0 mg, 10.0 mg, 20.0 mg, 40.0 mg, 5.0 mg, 20.0 mg/mL, 40.0 mg/mL, 4.0 mg/mL

Oral, Tablet, film coated - Oral, , Tablet, film coated, Tablet, Tablet - Oral, Tablet, film coated, extended release, Tablet, film coated, extended release - Oral, Suspension, Suspension - Oral, Tablet, orally disintegrating, Tablet, orally disintegrating - Oral, Tablet, coated, Tablet, coated - Oral, Periarticular, Tablet, film coated - Periarticular

Warnings

Vytorin Contraindications

Condition

Risk Level

Notes

Pulse Frequency

Do Not Combine

Pulse Frequency

Do Not Combine

Pulse Frequency

Do Not Combine

Pulse Frequency

Do Not Combine

Liver Diseases

Do Not Combine

There are 20 known major drug interactions with Vytorin.

Common Vytorin Drug Interactions

Drug Name

Risk Level

Description

Abemaciclib

Major

The serum concentration of Abemaciclib can be increased when it is combined with Simvastatin.

Amitriptyline

Major

The metabolism of Amitriptyline can be decreased when combined with Simvastatin.

Amoxapine

Major

The metabolism of Amoxapine can be decreased when combined with Simvastatin.

Astemizole

Major

The metabolism of Astemizole can be decreased when combined with Simvastatin.

Axitinib

Major

The serum concentration of Axitinib can be increased when it is combined with Simvastatin.

Vytorin Toxicity & Overdose Risk

The toxic dose of sitostanol in rats is greater than 2000mg/kg. In mice and dogs it is greater than 5000mg/kg and 3000mg/kg, respectively. One person has accidentally overdosed on sitostanol in clinical studies, but did not experience any adverse effects. Treatment for an overdose of sitostanol includes symptomatic care.

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Vytorin Novel Uses: Which Conditions Have a Clinical Trial Featuring Vytorin?

Currently, 8 clinical trials are underway to assess the potential of Vytorin to ameliorate sitosterols, Dietary Lipids and other associated conditions.

Condition

Clinical Trials

Trial Phases

Type 2 Diabetes

167 Actively Recruiting

Not Applicable, Phase 1, Phase 2, Phase 3, Phase 4, Early Phase 1

Diabetes

74 Actively Recruiting

Phase 1, Not Applicable, Phase 4, Phase 2, Phase 3

Homozygous Familial Hypercholesterolemia

2 Actively Recruiting

Phase 3

cholesterol

4 Actively Recruiting

Phase 3, Not Applicable

prophylaxis of cardiovascular event

0 Actively Recruiting

Physical Activity

24 Actively Recruiting

Not Applicable, Phase 1, Phase 2

Hypercholesterolemia

4 Actively Recruiting

Phase 1, Phase 3

Lipid-Lowering Therapy

0 Actively Recruiting

Cerebrovascular Disorders

2 Actively Recruiting

Phase 1, Not Applicable

Diet

5 Actively Recruiting

Not Applicable, Phase 1

Cardiovascular Events

4 Actively Recruiting

Not Applicable

Coronary heart disease

0 Actively Recruiting

Mixed Hyperlipidemia

0 Actively Recruiting

Peripheral Vascular Disease

6 Actively Recruiting

Phase 1, Phase 2, Not Applicable, Phase 4, Phase 3

Vytorin Reviews: What are patients saying about Vytorin?

5

Patient Review

11/24/2012

Vytorin for High Cholesterol

I experienced muscle weakness within months of starting this drug. Blood tests (Ck) also confirmed muscle damage, so stopped taking it after 18 months and transferred to the 10/20 dosage, which has been working out well so far.

5

Patient Review

9/1/2012

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

If I don't take this cholesterol medication, my levels will get as high as 400 or 500. That's not good for me, so I'm thankful for this medication.

5

Patient Review

11/24/2012

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

I take this in the morning because I can't take it at night - it makes me tired. However, when taken at night I get bad heartburn.

5

Patient Review

2/18/2013

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

I stopped taking this medicine after 19 months of use and immediately felt better. I was skeptical at first, but now I realize that the medicine was causing all of my problems.

5

Patient Review

12/31/2011

Vytorin for Homozygous Inherited High Blood Cholesterol

So far this medication is working well for me and I have not had any muscle problems with it.

4.7

Patient Review

10/1/2012

Vytorin for Homozygous Inherited High Blood Cholesterol

This lowered my cholesterol levels by 40 points in a short period of time, which was amazing.

4.7

Patient Review

7/15/2015

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

I've been using Vytorin for years without any problems. It's effective for me.

4.3

Patient Review

8/2/2012

Vytorin for High Cholesterol

This treatment lowered my cholesterol an impressive amount in a short period of time.

4.3

Patient Review

10/21/2011

Vytorin for Homozygous Inherited High Blood Cholesterol

4.3

Patient Review

12/20/2013

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

I hadn't tried this medication before, but my cholesterol and triglyceride levels were really high so I decided to give it a shot.

3.7

Patient Review

10/23/2012

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

Even with a strict diet, this medication didn't lower my cholesterol levels enough to make a difference. It also had no effect on my triglyceride levels.

3.7

Patient Review

11/8/2011

Vytorin for High Cholesterol

2.3

Patient Review

9/10/2012

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

Vytotin lowered my LDL cholesterol from 98 to 49 in just six weeks, and it stayed at around 40 after six months. My heart disease has actually reversed, and my Ebt scan now shows zero plaque. Plus, my carotid artery stenosis is reversing. I haven't experienced any discernable side effects, which is great.

2

Patient Review

12/24/2011

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

I didn't get any relief from this treatment and it was quite expensive.

1.7

Patient Review

10/17/2011

Vytorin for Combined High Blood Cholesterol and Triglyceride Level

1.3

Patient Review

2/18/2013

Vytorin for High Cholesterol

I've been taking Vytorin for years with no issues, but my doctor recently lowered the dosage. I'm happy to report that it's still just as effective.
image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about vytorin

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is Vytorin better than Lipitor?

"The study found that VYTORIN 10/40 mg decreased LDL cholesterol by 59 percent compared to 48 percent for Lipitor 40 mg in the subgroup of high risk patients with baseline LDL cholesterol values of 169 mg/dL and 175 mg/dL respectively (p<0.001)."

Answered by AI

What are side effects of Vytorin?

"difficulty urinating,

You may experience a headache, nausea, vomiting, diarrhea, dizziness, depression, memory problems, confusion, or difficulty urinating."

Answered by AI

What is Vytorin used for?

"Simvastatin belongs to a group of drugs known as "statins." It works by reducing the amount of cholesterol made by the liver.

This combination medication helps lower "bad" cholesterol and fats (such as LDL, triglycerides) and raise "good" cholesterol (HDL) in the blood. Ezetimibe works by reducing the amount of cholesterol your body absorbs from your diet. Simvastatin belongs to a group of drugs known as "statins." It works by reducing the amount of cholesterol made by the liver."

Answered by AI

What are the side effects of Vytorin?

"A headache, nausea, vomiting, diarrhea, dizziness, depression, memory problems, confusion may be caused by a concussion."

Answered by AI

What is the difference between Vytorin and Crestor?

"Vytorin was found to be more effective than Crestor at reducing LDL cholesterol by 52 to 61 percent depending on the dosage, according to a study funded by Merck and Schering-Plough."

Answered by AI

Why was Vytorin taken off the market?

"The US Food and Drug Administration (FDA) has not approved Zetia and Vytorin, Merck's medicines that are used to reduce the risk of cardiovascular events in patients with coronary heart disease. Feb 15, 2016"

Answered by AI

Clinical Trials for Vytorin

Image of VA Greater Los Angeles Healthcare System, West Los Angeles, CA in West Los Angeles, United States.

EBQI Strategies for Women's Health

Any Age
All Sexes
West Los Angeles, CA

Women Veterans are the fastest growing segment of VA users, with most users in midlife. This dramatic growth has created challenges for VA to ensure that appropriate services are available to meet women Veterans' needs, and that they will want and be able to use those services. Furthermore, few VA improvement efforts have focused on women Veterans' health and health care in midlife. The EMPOWER QUERI 3.0 Program is a cluster randomized type 3 hybrid implementation-effectiveness trial testing two strategies designed to support implementation and sustainment of evidence-based practices for women Veterans in at least 18 VA facilities from 4 regions.

Waitlist Available
Has No Placebo

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

Erin P Finley, PhD MPH

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Saskatoon Berries for Type 2 Diabetes

18 - 74
All Sexes
Winnipeg, Canada

Diabetes becomes epidemic in worldwide countries. Diabetes Canada indicated that 30% of adults in Manitoba are diabetes or prediabetes. Nine out of ten diabetic patients are type 2 diabetes (T2D). T2D is characterized by insulin resistance and obesity. Uncontrolled diabetes leads to serious consequences including heart attack, stroke, chronic renal failure, liver failure, blindness and low limb amputation. Most of hypoglycemic medications have certain side effects. Natural foods or nutraceuticals with hypoglycemic potential are expected to provide a safer management for diabetic patients. Saskatoon berry is a popular fruit in Canadian Prairie and Northern states in USA. Our previous studies demonstrated Saskatoon berry (SB) powder attenuated hyperglycemia, hyperlipidemia, insulin resistance, inflammation, liver steatosis and gut dysbiosis in diet-induced insulin resistant mice, a model for T2D. The findings of the glucose and lipid lowering or liver protective effects of SB powder have been supported by another group in Australia in high fat fed rats. Our preliminary studies in 20 healthy subjects demonstrated that dried whole SB (40 g/day for 10 weeks) significantly reduced fasting plasma glucose, total and LDL-cholesterol, systolic blood pressure, and increased plasma glucagon-like peptide compared to baseline, which was associated with increased intake of total fiber and decreased intake of saturated fat. The changes in metabolic and vascular variables significantly correlated with the alterations in gut microbiota The combination of findings suggest that SB is good candidate of prebiotic functional food as a supplemental remedy for reducing the risk for metabolic syndrome and preventing or managing T2D. The effect of Saskatoon berry and its products on metabolic disorders have not been studied in diabetic subjects. We propose to examine the effects of oral administration of freeze-dried whole SB on glucose metabolism, insulin resistance and gut microbiota in untreated prediabetes and new type 2 diabetic patients compared to a control dried fruit in a randomized controlled trial.

Waitlist Available
Dietary Supplement

Faculty of Health Sciences

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CX11 for Type 2 Diabetes

18 - 75
All Sexes
Birmingham, AL

This study is testing whether a new medication called CX11 works and is safe for participants with type 2 diabetes who have not reached good blood sugar control while taking a steady dose of metformin, with or without a steady dose of an SGLT2 inhibitor, for at least 90 days. The study is being done at multiple medical centers. Participants are assigned by chance (randomized) to different groups, and neither the participants nor the study staff know which group they're in (double-blind). The groups are compared side by side (parallel), and some participants will receive inactive pills (placebo) to help measure the true effect of the study drug. After screening, participants will be randomly placed into one of six groups, with equal chances of being in any group. Each group will receive a different dose of CX11 or a placebo. Treatment will last 24 weeks. After that, all participants will have a 2-week follow-up period to check on safety.

Phase 2
Waitlist Available

Central Research Associates - Flourish - PPDS (+29 Sites)

Corxel Pharmaceuticals

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Rosuvastatin for Cancer-Associated Blood Clots

18+
All Sexes
Boston, MA

Patients with cancer are at high risk for life-threatening venous thromboembolism (VTE) yet rarely receive anticoagulant prophylaxis due to bleeding risks. Thus, effective prophylaxis in oncology requires a method to reduce VTE without increasing hemorrhage. The primary aim of the Statin Therapy to Prevent Cancer Associated Venous Thromboembolism (STAT-CAT) trial is to test whether rosuvastatin 20 mg daily for 12 months compared to placebo can safely prevent VTE in patients with newly diagnosed or recently relapsed cancer who are at increased thrombotic risk, are not planned to be anticoagulated, and who do not otherwise take statin therapy.

Phase 4
Waitlist Available

Brigham and Women's Hospital (+1 Sites)

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Glucagon for Diabetes

18 - 45
All Sexes
Durham, NC

This study examines how glucagon works to regulate glucose metabolism, based on new findings that suggest glucagon signaling in the liver has more than one role, and that these multiple roles can be opposing in nature. Understanding this biology provides an opportunity to develop new generations of glucagon-based drugs that target specific pathways, making them more effective at controlling blood glucose. Participants will complete paired, 5-hour hyperinsulinemic glucose clamp visits in which they receive either glucagon or saline infusions while blood glucose is maintained and frequent blood samples are collected. The primary focus is whether coordinated glucagon and insulin signaling enhances hepatic insulin sensitivity.

Phase 1 & 2
Waitlist Available

Duke Center for Living

David D'Alessio, MD

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We made a collection of clinical trials featuring Vytorin, we think they might fit your search criteria.
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Adaptive Dietary Intervention for Type 2 Diabetes

18+
All Sexes
New York, NY

The investigators will examine the feasibility, acceptability, and effect of an adaptive dietary intervention over 24 weeks (12-week intervention, 12-week follow-up) among Asian Americans with Type 2 diabetes. Participants (N=120; 60 Chinese Americans and 60 Vietnamese Americans) will be 2:1 randomized to one of two arms: adaptive dietary intervention or standard of care (SC). The intervention will begin with continued glucose monitoring (CGM) use only during weeks 0-4. At week 4, participants who achieve the glycemic control goal (at least an 8% increase in time in range \[TIR\] from baseline) will continue with the CGM alone during weeks 4-12 ("CGM Alone"); otherwise, culturally and linguistically adapted glucose excursion minimization (GEM) will be augmented with CGM ("CGM-GEM").

Waitlist Available
Has No Placebo

NYU Langone Health

Yaguang Zheng, PhD, RN

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We made a collection of clinical trials featuring Vytorin, we think they might fit your search criteria.
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