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Clinical Trials in the USA / NCT07546929
Recruiting Phase 2

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

NCT07546929 · tracked via the Priya Life Science USA tracker
Sponsor
Housey Healthcare ULC
Phase
Phase 2
Started
2023-02-03
Last updated
2026-04-23

Condition(s) studied

Type 2 Diabetes

Investigational drug(s) / intervention(s)

HP-211Placebo

HP-211: HP-211 is an investigational botanical extract derived from Cichorium endivia var. latifolium, Lactuca sativa, and Artemisia dracunculus.

Placebo: Matching placebo administered orally twice daily (BID).

Study 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

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * 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. Key Exclusion Criteria: * Have known type 1 diabetes. * Diabetic complications * Have taken any oral (other than metformin) or injectable treatment (insulin or GLP-1 RA classes or other) for type 2 diabetes currently or for greater than a 4 week duration previously. Previous treatment must have been stopped at least 3 months prior to screening * Systolic blood pressure greater than 150 mmHg or a diastolic blood pressure greater than 100 mmHg at Visit 1 on average after three supine measurements, or a known history of renal artery stenosis. * At baseline, the QT interval corrected by Fridericia (QTcF) ECG findings (\>450 msec for males and \>470 msec for females), left bundle branch block, or cardiac arrhythmia requiring medical or surgical treatment within 6 months prior to Visit 1 on the ECG.

Primary outcome measure(s)

Trial sites (25)

FacilityCityRegionStatus
Alliance Clinical Canoga Park (Hope Clinical Research) Canoga Park California Recruiting
Universal Axon Clinical Research Doral Florida Recruiting
Velocity Clinical Research New Smyrna Beach Edgewater Florida Recruiting
Southwest General Healthcare Center Fort Myers Florida Recruiting
Avantis Clinical Research Miami Florida Recruiting
IMIC Research Miami Florida Recruiting
South Broward Research Miramar Florida Recruiting
David Kavtaradze MD InC Cordele Georgia Recruiting
AMR Clinical - El Dorado El Dorado Kansas Recruiting
Tandem Clinical Research (Interspond) Marrero Louisiana Recruiting
Arcturus Healthcare, PLC, Troy Internal Medicine Research Division Troy Michigan Recruiting
Velocity Clinical Research Norfolk Norfolk Nebraska Recruiting
Alliance Clinical Las Vegas (Excel Clinical Research) Las Vegas Nevada Recruiting
Diabetes & Endocrinology Associates of Stark County, Inc. Canton Ohio Recruiting
Advanced Medical Research Maumee Ohio Recruiting
Velocity Clinical Research Providence East Greenwich Rhode Island Recruiting
Velocity Clinical Research Dallas Dallas Texas Recruiting
Tekton Research Irving Texas Recruiting
Alliance Clinical Lewisville (Epic Clinical Research) Lewisville Texas Recruiting
Tekton Research McKinney Texas Recruiting
Tekton Research San Antonio Texas Recruiting
Simcare Medical Research, LLC. Sugar Land Texas Recruiting
Velocity Clinical Research Waco Waco Texas Recruiting
Burke Internal Medicine & Research Burke Virginia Recruiting
Tekton Research Midlothian Virginia Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07546929 on ClinicalTrials.gov ↗ ← All trials in the USA