Recruiting
Phase 2

HP-211

Sponsor:

Housey Healthcare ULC

Code:

NCT07546929

Conditions

Type 2 Diabetes

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

HP-211

Placebo

Study Details

Brief 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.

Conditions

Type 2 Diabetes

Study ID

NCT07546929

Start date

Feb 3, 2023

Status verified date

Apr, 2026

Completion date

Oct, 2026

Anticipated

Primary completion date

Oct, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

300 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

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

Interventions

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).

Primary outcome measure

  • Change from Baseline in Hemoglobin A1c (HbA1c) [ Time Frame: After 12 weeks of treatment. ]

Central Contacts and Locations

Central contacts

Locations

Alliance Clinical Canoga Park (Hope Clinical Research)

Recruiting

Canoga Park, California, United States, 91303

Contacts

Principal Investigator:

Hessam Aazami, MD

Universal Axon Clinical Research

Recruiting

Doral, Florida, United States, 33166

Contacts

Principal Investigator:

Luis Martinez, MD

Velocity Clinical Research New Smyrna Beach

Recruiting

Edgewater, Florida, United States, 32132

Contacts

Principal Investigator:

Margaret Chang, MD

Southwest General Healthcare Center

Recruiting

Fort Myers, Florida, United States, 33907

Contacts

Principal Investigator:

Jose Rodriguez, MD

Avantis Clinical Research

Recruiting

Miami, Florida, United States, 33155

Contacts

Principal Investigator:

Jacqueline Diaz, MD

IMIC Research

Recruiting

Miami, Florida, United States, 33176

Contacts

Principal Investigator:

Ramon Leon, MD

South Broward Research

Recruiting

Miramar, Florida, United States, 33027

Contacts

Principal Investigator:

Kenneth Blaze, DO

David Kavtaradze MD InC

Recruiting

Cordele, Georgia, United States, 31015

Contacts

Principal Investigator:

David Kavtaradze, MD

AMR Clinical - El Dorado

Recruiting

El Dorado, Kansas, United States, 67042

Contacts

Principal Investigator:

Michael Rausch, MD

Tandem Clinical Research (Interspond)

Recruiting

Marrero, Louisiana, United States, 70072

Contacts

Principal Investigator:

Adil Fatakia, MD

Arcturus Healthcare, PLC, Troy Internal Medicine Research Division

Recruiting

Troy, Michigan, United States, 48098

Contacts

Principal Investigator:

Neil Fraser, MD

Velocity Clinical Research Norfolk

Recruiting

Norfolk, Nebraska, United States, 68701

Contacts

Principal Investigator:

Charles Harper, MD

Alliance Clinical Las Vegas (Excel Clinical Research)

Recruiting

Las Vegas, Nevada, United States, 89109

Contacts

Principal Investigator:

Robby Quintos, MD

Diabetes & Endocrinology Associates of Stark County, Inc.

Recruiting

Canton, Ohio, United States, 44718

Contacts

Principal Investigator:

Arvind Krishna, MD

Advanced Medical Research

Recruiting

Maumee, Ohio, United States, 43537

Contacts

Principal Investigator:

Nizar Daboul, MD

Velocity Clinical Research Providence

Recruiting

East Greenwich, Rhode Island, United States, 02818

Contacts

Principal Investigator:

David Fried, MD

Velocity Clinical Research Dallas

Recruiting

Dallas, Texas, United States, 75230

Contacts

Principal Investigator:

Dan Lender, MD

Tekton Research

Recruiting

Irving, Texas, United States, 75039

Contacts

Principal Investigator:

Samata Basani, MD

Alliance Clinical Lewisville (Epic Clinical Research)

Recruiting

Lewisville, Texas, United States, 75057

Contacts

Principal Investigator:

Manjoo Sharma, MD

Tekton Research

Recruiting

McKinney, Texas, United States, 75069

Contacts

Principal Investigator:

Muhammad Siddiqui, MD

Tekton Research

Recruiting

San Antonio, Texas, United States, 78258

Contacts

Principal Investigator:

Jara McDonald, MD

Simcare Medical Research, LLC.

Recruiting

Sugar Land, Texas, United States, 77478

Contacts

Principal Investigator:

Imran Siddiqui, MD

Velocity Clinical Research Waco

Recruiting

Waco, Texas, United States, 76710

Contacts

Principal Investigator:

Gregg Lucksinger, MD

Burke Internal Medicine & Research

Recruiting

Burke, Virginia, United States, 22015

Contacts

Principal Investigator:

Nabil Andrawis, MD

Tekton Research

Recruiting

Midlothian, Virginia, United States, 23112

Contacts

Principal Investigator:

Ben Phillips, MD

More Information

Sponsor

Housey Healthcare ULC

Last update posted

Apr 23, 2026

Last verified

Apr, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Housey Healthcare ULC on 2026-04-23.