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NCT07546929ClinicalTrials.gov

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

قيد التجنيديقبل مشاركين الآن، وفقاً لسجل السجل.
التواصل مع هذه الدراسة

باختصار

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…

المرحلة 2مطلوب 300 مشارك25 موقعاًدولة واحدة

الفئات

مسجَّلة في سجل واحد

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How this study is set up

The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.

  • Not stated: Registered after enrolment began (about 1175 days after the recorded start)First posted 2026-04-23; recorded start 2023-02-03
  • Present: Has a defined primary outcomeA primary outcome measure is listed in the record
  • Present: The primary outcome states a time frameThe primary outcome measure records a time frame
  • Present: Participants are randomly assignedAllocation is recorded as randomised
  • Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one study arm
  • Present: Uses blinding (masking)A masking level is recorded in the record
  • Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
  • Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
  • Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
  • Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
  • Not stated: No other studies from this sponsor are in this databaseCounted from the lead sponsor named in the record (Housey Healthcare ULC)
  • Not stated: No posted results from this sponsor are in this database yetBased on the sponsor’s studies in this database
  • The record lists 1 condition.
  • Lead sponsor type recorded as: industry.
  • Intervention regulatory context: investigational, within a phased regulatory pathway.

Trial stature

Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.

Methodological rigourDEFINITIVE

A definitive-grade design for a phase 2 study, judged from its ClinicalTrials.gov record.

How this score is built
  • Randomised allocation20/20

    Participants are randomly allocated between arms

  • Blinding20/20

    Quadruple-blind

  • Control arm13/15

    Placebo / sham control arm

  • Primary-outcome specificity10/10

    Named primary outcome with a defined time frame

  • Endpoint type3/10

    Surrogate or intermediate endpoint (conservative default)

  • Multi-centre8/8

    Multi-centre: 25 sites

  • Data monitoring committee7/7

    A data monitoring committee is in place

  • Prospective registration0/5

    Registered more than 30 days after the study start

  • Protocol / SAP posted0/5

    No protocol or SAP posted to the registry

ScaleMEDIUM

A medium-sized study: 300 participants (target), run at 25 sites.

How this score is built
  • Enrolment24/40

    300 participants (target)

  • Site count17/25

    25 sites

  • Country count0/15

    Single country

  • Planned duration9/10

    Planned over about 45 months

  • Sponsor scale0/10

    Housey Healthcare ULC has led 1 trials in our corpus

Investigator standingUNKNOWN

We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.

How this score is built
  • Investigator standing0/100

    No investigator recorded in the registry for this trial

These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.

ملخص

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.

After consumption of a meal, pancreatic secretions of various digestive enzymes result in the breakdown of carbohydrates into monosaccharides such as glucose. These sugars are subsequently absorbed through the intestinal lumen, resulting in an increased plasma glucose concentration. In response to high glucose levels, pancreatic beta cells are stimulated to release insulin, a hormone which circulates through the bloodstream and binds to insulin-responsive cells including adipocytes (fat tissue), myocytes (muscle), hepatocytes (liver), and neurons in various regions of the brain. The resulting insulin-mediated signaling cascade initiates intracellular glucose uptake within peripheral tissues leading to a corresponding decrease in circulating plasma glucose. In insulin responsive cells the stimulation of glucose uptake begins after the binding of insulin to Insulin Receptors (IR). These receptors are found on the membrane surface of cells in insulin-responsive tissues. The IR consists of an extracellular domain which binds to insulin, and an intracellular domain that has a protein tyrosine kinase activity. The binding of Insulin to the IR initiates a series of autophosphorylation events within the protein kinase domain that permit interaction and phosphorylation of downstream signaling proteins in the cell that mediate the cellular response to insulin. The resulting signaling complex includes proteins in the Insulin Receptor Substrate (IRS) family known as IRS-1 and IRS-2. These key targets of the insulin signaling pathway link IR activation to downstream signaling cascades that mediate intracellular processes including GLUT4-mediated glucose uptake. Prediabetes and Type II diabetes involve an impaired post-receptor response to insulin that hinders the glucose uptake response after meal consumption. Chronic hyperglycemia and the resulting compensatory hyperinsulinemia promote a cohort of acute and chronic sequelae including cardiovascular disease, liver complications, central nervous system degeneration, abnormal cellular growth resulting in an increased incidence of several forms of cancer, and hyperglycemic osmotic stress. HP-211 is a botanical extract containing active ingredients derived from edible plant species herbs and vegetables present in normal diets.In vitro, HP-211, has marked effects on the IRS-2 branch of the insulin signaling cascade to enhance downstream insulin signaling. HP-211 has been shown in animal models to increase glucose uptake in peripheral tissues and decrease circulating blood glucose and triglyceride concentrations. Regular supplementation of the diet with HP-211 may reduce the incidence of associated prediabetic and diabetic complications, resulting in an increased quality of life for patients without resorting to current anti-diabetic prescription drugs that may have undesirable side effects. Hypotheses HP-211 will reduce postprandial glucose and insulin levels in subjects with new onset type 2 diabetes as well as subjects with existing type 2 diabetes who are not well-controlled despite using the maximum tolerated dose of metformin. The reduction in glucose and insulin will be relatively greater in insulin-resistant than insulin-sensitive subjects. Over a 90-day treatment period, these effects will lead to a reduction in hemoglobin A1c (HbA1c), a measure of long-term blood glucose control. Subjects will take 0, 1, 2, or 3 tablets of HP-211 in the morning and evening, preferably at least 60 minutes before a meal. Hemoglobin A1c and numerous additional measures of glucose control as well as safety studies will be determined.

الحالات

  • Type 2 Diabetes

الأهلية

الأهلية
الجنسالجميع
الأعمار18 Yearsلا حد أقصى
المتطوعون الأصحّاءلا

الأهلية كما كُتبت في السجل

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.

الأهلية في عبارات بسيطة

لم تُقسَّم معايير هذا السجل إلى عبارات منفصلة بعد. نص السجل أعلاه كامل وهو النسخة المُعتمَدة.

تصميم الدراسة

تصميم الدراسة
نوع الدراسةتدخّلية
المرحلةالمرحلة 2
التخصيصمعشّاة
نموذج التدخّلPARALLEL
الغرض الأساسيTREATMENT
التعميةQUADRUPLE (4)
التجنيدمطلوب 300 مشارك

الجهة الراعية والمتعاونون

  • Housey Healthcare ULC الجهة الراعية

الأذرع والتدخلات

  • HP-211 Dose Level 2EXPERIMENTAL

    HP-211 1.96grams BID

  • HP-211 Dose Level 3EXPERIMENTAL

    HP-211 2.94grams BID

  • HP-211 Dose Level 4PLACEBO_COMPARATOR

    Placebo BID

  • HP-211 Dose Level 1EXPERIMENTAL

    HP-211 0.98grams BID

التدخلات

  • دواء HP-211

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

  • دواء Placebo

    Matching placebo administered orally twice daily (BID).

مقاييس النتائج

  1. مقياس النتيجة الأولي

    Change from Baseline in Hemoglobin A1c (HbA1c)

    Least squares mean change from baseline in HbA1c at Week 12, analyzed using a mixed model for repeated measures (MMRM).

    الإطار الزمني After 12 weeks of treatment.

  2. مقياس النتيجة الثانوي

    Change from Baseline in Fasting Blood Glucose

    Change from baseline in fasting blood glucose levels.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  3. مقياس النتيجة الثانوي

    Change from Baseline in 7-Point Self-Monitored Blood Glucose (SMBG) Profile

    Mean change from baseline in 7-point SMBG profile, including pre-meal and 2-hour postprandial glucose measurements.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  4. مقياس النتيجة الثانوي

    Proportion of Participants Achieving HbA1c <7.0%

    Percentage of participants achieving HbA1c less than 7.0%.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  5. مقياس النتيجة الثانوي

    Proportion of Participants Achieving HbA1c <6.5%

    Percentage of participants achieving HbA1c less than 6.5%.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  6. مقياس النتيجة الثانوي

    Incidence of Hypoglycemia Events (Levels 1-3) -Treatment emergent adverse events (TEAEs) -Serious Adverse Events (SAEs)

    Number and percentage of participants experiencing hypoglycemia events classified as Levels 1 through 3.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  7. مقياس النتيجة الثانوي

    Change from Baseline in Body Weight

    Change from baseline in body weight measured in kilograms.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  8. مقياس النتيجة الثانوي

    Incidence of Treatment-Emergent Adverse Events (TEAEs)

    Number and percentage of participants experiencing treatment-emergent adverse events.

    الإطار الزمني From first dose through Week 16

  9. مقياس النتيجة الثانوي

    Incidence of Serious Adverse Events (SAEs)

    Number and percentage of participants experiencing serious adverse events.

    الإطار الزمني From first dose through Week 16

  10. مقياس النتيجة الثانوي

    Change from Baseline in Diabetes Treatment Satisfaction Questionnaire (DTSQs/DTSQc) Score

    Change from baseline in patient-reported treatment satisfaction using DTSQs and DTSQc instruments. * The DTSQs score ranges from 0 to 6 per item with totals ranging from 0 to 36, with higher scores indicating greater treatment satisfaction. * The DTSQc measures change in satisfaction, with item scores typically ranging from -3 to +3 and totals ranging from -18 to +18, where positive scores indicate improvement and negative scores indicate worsening of treatment satisfaction.

    الإطار الزمني Week 12

  11. مقياس النتيجة الثانوي

    Change from Baseline in Audit of Diabetes-Dependent Quality of Life (ADD-QOL) Score

    Change from baseline in patient-reported quality of life using the ADD-QOL instrument. * Change from baseline in patient-reported treatment satisfaction using the Diabetes Treatment Satisfaction Questionnaire status version (DTSQs) and change version (DTSQc). * The DTSQs total score ranges from 0 to 36, with higher scores indicating greater treatment satisfaction. * The DTSQc measures change in satisfaction, with item scores typically ranging from -3 to +3, where positive scores indicate improvement and negative scores indicate worsening of treatment satisfaction.

    الإطار الزمني Week 12

  12. مقياس نتيجة آخر

    Exploratory: Change from Baseline in High-Sensitivity C-Reactive Protein (hs-CRP)

    Change from baseline in hs-CRP levels.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  13. مقياس نتيجة آخر

    Exploratory: Change from Baseline in Lipid Profile Parameters

    Change from baseline in lipid parameters including total cholesterol, LDL, HDL, and triglycerides.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  14. مقياس نتيجة آخر

    Exploratory: Exploratory: Change from Baseline in Mean Glucose (CGM)

    Change from baseline in mean glucose measured by continuous glucose monitoring (CGM), reported in mg/dL.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  15. مقياس نتيجة آخر

    Exploratory: Change from Baseline in Time in Range (CGM)

    Change from baseline in time in target glucose range (70-180 mg/dL) measured by continuous glucose monitoring (CGM), reported as percentage of time within range.

    الإطار الزمني After 12 weeks of treatment and and after 4 weeks of the withdrawal phase.

  16. مقياس نتيجة آخر

    Exploratory: Change from Baseline in Glucose Excursion During 75 g Oral Glucose Tolerance Test (OGTT)

    Change from baseline in glucose excursion during OGTT, assessed using serial glucose measurements over 0-120 minutes.

    الإطار الزمني Week 12

  17. مقياس نتيجة آخر

    Exploratory: Change from Baseline in Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)

    Change from baseline in insulin resistance as measured by HOMA-IR.

    الإطار الزمني Week 12

  18. مقياس نتيجة آخر

    Exploratory: Change from Baseline in Matsuda Index

    Change from baseline in insulin sensitivity as measured by the Matsuda Index.

    الإطار الزمني Week 12

التواريخ

التواريخ
تاريخ البدء3 فبراير 2023 (فعلي)
الإتمام الأولي1 أكتوبر 2026 (تقديري)
الإتمام1 أكتوبر 2026 (تقديري)
أول نشر23 أبريل 2026 (فعلي)
آخر تحديث23 أبريل 2026
النتائج منشورةغير مذكور في سجل السجل
آخر تأكيد للحالةأبريل 2026

فعلي يعني أن الحدث وقع. تقديري يعني أن الجهة الراعية تتوقعه. للكلمتين معنيان مختلفان.

المواقع

25 موقعاً قيد التجنيد

United States

United States
المنشأةالمدينةالولاية أو المنطقةالحالة
Burke Internal Medicine & ResearchBurkeVirginiaقيد التجنيد
Alliance Clinical Canoga Park (Hope Clinical Research)Canoga ParkCaliforniaقيد التجنيد
Diabetes & Endocrinology Associates of Stark County, Inc.CantonOhioقيد التجنيد
David Kavtaradze MD InCCordeleGeorgiaقيد التجنيد
Velocity Clinical Research DallasDallasTexasقيد التجنيد
Universal Axon Clinical ResearchDoralFloridaقيد التجنيد
Velocity Clinical Research ProvidenceEast GreenwichRhode Islandقيد التجنيد
Velocity Clinical Research New Smyrna BeachEdgewaterFloridaقيد التجنيد
AMR Clinical - El DoradoEl DoradoKansasقيد التجنيد
Southwest General Healthcare CenterFort MyersFloridaقيد التجنيد
Tekton ResearchIrvingTexasقيد التجنيد
Alliance Clinical Las Vegas (Excel Clinical Research)Las VegasNevadaقيد التجنيد
Alliance Clinical Lewisville (Epic Clinical Research)LewisvilleTexasقيد التجنيد
Tandem Clinical Research (Interspond)MarreroLouisianaقيد التجنيد
Advanced Medical ResearchMaumeeOhioقيد التجنيد
Tekton ResearchMcKinneyTexasقيد التجنيد
Avantis Clinical ResearchMiamiFloridaقيد التجنيد
IMIC ResearchMiamiFloridaقيد التجنيد
Tekton ResearchMidlothianVirginiaقيد التجنيد
South Broward ResearchMiramarFloridaقيد التجنيد
Velocity Clinical Research NorfolkNorfolkNebraskaقيد التجنيد
Tekton ResearchSan AntonioTexasقيد التجنيد
Simcare Medical Research, LLC.Sugar LandTexasقيد التجنيد
Arcturus Healthcare, PLC, Troy Internal Medicine Research DivisionTroyMichiganقيد التجنيد
Velocity Clinical Research WacoWacoTexasقيد التجنيد

مستندات الدراسة

لا تُرتبط أي مستندات في سجل السجل هذا.

التغيّرات عبر الزمن

لم تُسجَّل أي تغييرات منذ أن أدرجنا هذا السجل لأول مرة.

يُسجَّل تغيير في كل مرة تحدّث فيها الجهة الراعية سجل السجل. تظهر هنا الحالة والتواريخ والتجنيد والمواقع كلما تغيّرت.