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HP-211 Safety and Proof of Concept Dose Ranging Study in Patients With Type 2 Diabetes

Status: Recruiting
Location: See all (25) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Blood sugar levels are controlled by insulin, a hormone made by cells in the pancreas. After a meal, carbohydrates are broken down into glucose which is absorbed from the intestine into the blood leading to a rise in glucose (blood sugar) which triggers the secretion of insulin. Insulin binds to cells in several tissues including liver, muscle, and fat, triggering cells to take up glucose and bring the blood glucose level back to normal. A high blood sugar level is known as diabetes. The most common form of diabetes, type 2 diabetes, is caused by insulin resistance; that is, a reduced ability of insulin to stimulate glucose uptake into cells. The body compensates for insulin resistance by making more insulin; type 2 diabetes occurs when the pancreas can no longer make enough insulin to control blood glucose. The high blood glucose and insulin levels lead to long-term complications such as heart attacks, kidney failure, reduced sensation and poor circulation in the feet and legs. High insulin levels also increase the incidence of cancers, stroke, and dementia. Reducing blood glucose levels with oral medications and insulin reduces risk of diabetic complications. There are several types of oral medications available for treating diabetes; however, they do not always control blood glucose adequately. In addition, these drugs have complications and are not used to treat insulin resistance and prediabetes - a condition when blood glucose is higher than normal but not high enough to be classified as diabetes. Prediabetes often progresses to diabetes over a period of months or years. Effective and safe treatments for insulin resistance may prevent the onset of diabetes or even reverse diabetes if diagnosed in its early stages before substantial damage to the pancreas has occurred. HP-211 is a botanical extract whose active ingredients are derived from herbs and vegetables present in normal diets. HP-211 has been shown in laboratory studies in cell culture, in animal studies, and in a previous Phase 1 study to enhance the ability of insulin to stimulate glucose uptake into cells. Thus, HP-211 may reduce the blood glucose and circulating insulin levels of subjects with type 2 diabetes after a meal. HP-211 may also reduce glucose and insulin responses to a greater extent in insulin-resistant as compared to insulin-sensitive subjects. Subjects will take 0, 1, 2 or 3 tablets of HP-211 in the morning and evening for 90 days. Hemoglobin A1c (HbA1c, or A1c), a measure of the average amount of glucose present in the blood, will be measured during the trial period.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Have type 2 diabetes for greater than 3 months and no longer than 5 years by history prior to entering the trial, based upon ADA disease diagnostic criteria.

• Have an HbA1c \> 6.5% and ≤ 10% as determined by the central lab at Visit 1 (Screening).

• Have been on a stable maximum dose of metformin for at least 3 months prior to entering the study or have been on stable therapy of diet and exercise only for at least 3 months. Stable treatment is defined as no change in treatment or dose in the last 3 months.

Locations
United States
California
Alliance Clinical Canoga Park (Hope Clinical Research)
RECRUITING
Canoga Park
Florida
Universal Axon Clinical Research
RECRUITING
Doral
Velocity Clinical Research New Smyrna Beach
RECRUITING
Edgewater
Southwest General Healthcare Center
RECRUITING
Fort Myers
Avantis Clinical Research
RECRUITING
Miami
IMIC Research
RECRUITING
Miami
South Broward Research
RECRUITING
Miramar
Georgia
David Kavtaradze MD InC
RECRUITING
Cordele
Kansas
AMR Clinical - El Dorado
RECRUITING
El Dorado
Louisiana
Tandem Clinical Research (Interspond)
RECRUITING
Marrero
Michigan
Arcturus Healthcare, PLC, Troy Internal Medicine Research Division
RECRUITING
Troy
Nebraska
Velocity Clinical Research Norfolk
RECRUITING
Norfolk
Nevada
Alliance Clinical Las Vegas (Excel Clinical Research)
RECRUITING
Las Vegas
Ohio
Diabetes & Endocrinology Associates of Stark County, Inc.
RECRUITING
Canton
Advanced Medical Research
RECRUITING
Maumee
Rhode Island
Velocity Clinical Research Providence
RECRUITING
East Greenwich
Texas
Velocity Clinical Research Dallas
RECRUITING
Dallas
Tekton Research
RECRUITING
Irving
Alliance Clinical Lewisville (Epic Clinical Research)
RECRUITING
Lewisville
Tekton Research
RECRUITING
Mckinney
Tekton Research
RECRUITING
San Antonio
Simcare Medical Research, LLC.
RECRUITING
Sugar Land
Velocity Clinical Research Waco
RECRUITING
Waco
Virginia
Burke Internal Medicine & Research
RECRUITING
Burke
Tekton Research
RECRUITING
Midlothian
Contact Information
Primary
Housey Study Info
StudyInfo@housey.com
(248) 663-7000
Time Frame
Start Date: 2023-02-03
Estimated Completion Date: 2026-10
Participants
Target number of participants: 300
Treatments
Experimental: HP-211 Dose Level 1
HP-211 0.98grams BID
Experimental: HP-211 Dose Level 2
HP-211 1.96grams BID
Experimental: HP-211 Dose Level 3
HP-211 2.94grams BID
Placebo_comparator: HP-211 Dose Level 4
Placebo BID
Sponsors
Leads: Housey Healthcare ULC

This content was sourced from clinicaltrials.gov