NCT07546929ClinicalTrials.gov
HP-211 Safety and Proof of Concept Dose Ranging Study in Patients With Type 2 Diabetes
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
- ClinicalTrials.govNCT07546929فتح هذا السجل في ClinicalTrials.govتمت المزامنة قبل شهرين
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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.
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
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
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.
الحالات
- Type 2 Diabetes
الأهلية
| الجنس | الجميع |
|---|---|
| الأعمار | 18 Years – لا حد أقصى |
| المتطوعون الأصحّاء | لا |
الأهلية كما كُتبت في السجل
الأهلية في عبارات بسيطة
لم تُقسَّم معايير هذا السجل إلى عبارات منفصلة بعد. نص السجل أعلاه كامل وهو النسخة المُعتمَدة.
تصميم الدراسة
| نوع الدراسة | تدخّلية |
|---|---|
| المرحلة | المرحلة 2 |
| التخصيص | معشّاة |
| نموذج التدخّل | PARALLEL |
| الغرض الأساسي | TREATMENT |
| التعمية | QUADRUPLE (4) |
| التجنيد | مطلوب 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
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.
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.
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.
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.
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.
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.
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.
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
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
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
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
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.
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.
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.
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.
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
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
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
| تاريخ البدء | 3 فبراير 2023 (فعلي) |
|---|---|
| الإتمام الأولي | 1 أكتوبر 2026 (تقديري) |
| الإتمام | 1 أكتوبر 2026 (تقديري) |
| أول نشر | 23 أبريل 2026 (فعلي) |
| آخر تحديث | 23 أبريل 2026 |
| النتائج منشورة | غير مذكور في سجل السجل |
| آخر تأكيد للحالة | أبريل 2026 |
فعلي يعني أن الحدث وقع. تقديري يعني أن الجهة الراعية تتوقعه. للكلمتين معنيان مختلفان.
المواقع
25 موقعاً قيد التجنيد
United States
| المنشأة | المدينة | الولاية أو المنطقة | الحالة |
|---|---|---|---|
| Burke Internal Medicine & Research | Burke | Virginia | قيد التجنيد |
| Alliance Clinical Canoga Park (Hope Clinical Research) | Canoga Park | California | قيد التجنيد |
| Diabetes & Endocrinology Associates of Stark County, Inc. | Canton | Ohio | قيد التجنيد |
| David Kavtaradze MD InC | Cordele | Georgia | قيد التجنيد |
| Velocity Clinical Research Dallas | Dallas | Texas | قيد التجنيد |
| Universal Axon Clinical Research | Doral | Florida | قيد التجنيد |
| Velocity Clinical Research Providence | East Greenwich | Rhode Island | قيد التجنيد |
| Velocity Clinical Research New Smyrna Beach | Edgewater | Florida | قيد التجنيد |
| AMR Clinical - El Dorado | El Dorado | Kansas | قيد التجنيد |
| Southwest General Healthcare Center | Fort Myers | Florida | قيد التجنيد |
| Tekton Research | Irving | Texas | قيد التجنيد |
| Alliance Clinical Las Vegas (Excel Clinical Research) | Las Vegas | Nevada | قيد التجنيد |
| Alliance Clinical Lewisville (Epic Clinical Research) | Lewisville | Texas | قيد التجنيد |
| Tandem Clinical Research (Interspond) | Marrero | Louisiana | قيد التجنيد |
| Advanced Medical Research | Maumee | Ohio | قيد التجنيد |
| Tekton Research | McKinney | Texas | قيد التجنيد |
| Avantis Clinical Research | Miami | Florida | قيد التجنيد |
| IMIC Research | Miami | Florida | قيد التجنيد |
| Tekton Research | Midlothian | Virginia | قيد التجنيد |
| South Broward Research | Miramar | Florida | قيد التجنيد |
| Velocity Clinical Research Norfolk | Norfolk | Nebraska | قيد التجنيد |
| Tekton Research | San Antonio | Texas | قيد التجنيد |
| Simcare Medical Research, LLC. | Sugar Land | Texas | قيد التجنيد |
| Arcturus Healthcare, PLC, Troy Internal Medicine Research Division | Troy | Michigan | قيد التجنيد |
| Velocity Clinical Research Waco | Waco | Texas | قيد 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.