- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04938388
Comparison of Oral Semaglutide w/ Placebo- Treatment for Latino Adults w/T2 Diabetes Receiving Enhanced Lifestyle Care
Comparison of Oral Semaglutide With Matched Oral Semaglutide Placebo as an Early Treatment for Latino Adults With Type 2 Diabetes Receiving Enhanced Lifestyle Care
Study Overview
Status
Intervention / Treatment
Detailed Description
Oral Semaglutide is the first oral formulation of a glucagon-like peptide-1 (GLP-1) receptor agonist developed for the treatment of type 2 diabetes (T2D). Monotherapy with once-daily oral Semaglutide has been shown to provide superior and dose-dependent decreases in HbA1c compared with placebo, and superior decreases in bodyweight in patients with T2D whose glycaemia was insufficiently controlled on diet and exercise. Recently, in patients with T2D and chronic kidney disease, Semaglutide was also effective in improving glycemic control and bodyweight with a low risk of hypoglycemia compared to placebo. Oral Semaglutide has also been shown to be superior to Sitagliptin. Results from the PIONEER 6 trial showed that no increased risk for major cardiovascular events was observed with oral Semaglutide in patients with T2D at high cardiovascular (CV) risk. In that study, Semaglutide reduced CV death and all- cause mortality by nearly 50% versus placebo after a median follow-up of 15.9 months. Therefore based on the evidence from the PIONEER trials, oral Semaglutide is likely to offer significant benefits for adults with T2D.
However in the United States (US), members of racial and ethnic minority groups are disproportionally affected by T2D and there is a paucity of information on what the potential impact of novel therapies such as oral Semaglutide might be for these populations. For example, the prevalence of both diagnosed and undiagnosed T2D is nearly twice as high among Mexican- origin Hispanic/Latino (hereafter Latino) adults compared to non-Latino whites. Likewise, rates of diabetes-related complications (including premature death from diabetes, acute stroke and end- stage renal disease) are also higher among Latino adults compared to their non-Latino white counterparts. For Latinos and other US minorities, beyond genetics and biological factors, it is recognized that sociocultural influences are also important factors in determining an individual's response to a therapy. In addition, self-identified race correlates with ancestry, which determines genomic variation, but this does not necessarily predict the response to a particular drug, nor can it be assumed that responses are similar between different races. As a corollary, being uninsured or a Medicaid recipient presents formidable challenges to improving cost-effective outcomes for people with diabetes. Currently, in the US, more than 29 million people are uninsured, with substantial inequalities in access to health care along economic, gender, racial, and ethnic lines. Racial and ethnic minority groups in the US also receive lower quality of health care compared with their white counterparts and disparities exist in the burden and cost of diabetes care for Medicare recipients. Identifying sub-groups with especially high risk of complications early in the course of T2D will also help clinicians to offer more cost-effective therapies. In addition, regulatory and policy decisions are increasingly based on a continuum of data from intensively monitored randomized clinical trials (RCTs) to real-world evidence (RWE), i.e., from tightly controlled, homogeneous populations to broader ones seen in usual clinical practice.
US minorities commonly live in "poorer" neighborhood environments with respect to access to healthy food sources, places to exercise or safety from crime. Plant-based dietary foods have the potential to help manage several major chronic diseases, including T2D. For underserved populations with T2D, food insecurity and low socioeconomic status are frequent barriers to nutrition-based self-management.
As a consequence, Sansum Diabetes Research Institute (SDRI) has recently created Farming for Life, which provides medically prescribed produce to Latino adults with non-insulin treated T2D. Farming for Life uses prescriptions of predominantly organic vegetable produce, as studies have shown that organic crops have higher concentrations of antioxidants and a lower incidence of pesticide residues than non-organic crops. There is growing evidence of an association between pesticide exposure and T2D risk.
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
California
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Santa Barbara, California, United States, 93105
- Sansum Diabetes Research Institute
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals ≥ 18 years of age at enrollment.
- Self-reported Hispanic/Latino heritage.
- Established diagnosis of T2D for at least 3 months prior to enrollment date.
- HbA1c > 7.5% and ≤ 10.0% (58-86 mmol/mol) within the previous 6 months.
- T2D treated with lifestyle alone or lifestyle + Metformin within the past 6 months prior to screening.
- Ability to provide informed consent before any trial-related activities. Trial-related activities are any procedure that would not have been performed during normal management of the subject.
- Based on the research staff's judgment, participant or participant's representative must have a good understanding, ability, and willingness to adhere to the protocol, including performance of self-monitored data collection during the wearable device portion of the study.
Exclusion Criteria:
- Type 1 diabetes or a history of diabetic ketoacidosis.
- T2D treated with oral medicines other than Metformin or any injectable GLP-1 receptor agonist or insulin within the past 6 months prior to screening.
- Life expectancy < 12 months.
- Any active clinically significant physical or mental disease or disorder which, in the investigator's opinion, could interfere with the participation in the study.
- History of major surgical procedures involving the stomach potentially affecting absorption of trial product (e.g., subtotal and total gastrectomy, sleeve gastrectomy, gastric bypass surgery).
- Untreated pre-proliferative or proliferative retinopathy or maculopathy due to diabetes.
- Renal impairment, defined as estimated glomerular filtration rate <30 mL/min/1.73 m2.
- Personal or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia syndrome type 2.
- Language barriers precluding comprehension of study activities and informed consent.
- Participation in other research studies involving medication or device within 1 month prior to enrollment.
- Known or suspected abuse of alcohol, narcotics, or illicit drugs.
- Known or suspected allergy to OS, excipients, or related products.
- Previous participation in this trial whether screened or randomized.
- Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures.
- The receipt of any investigational drug (within 12 months) prior to this trial.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Oral Semaglutide (OS) with Enhanced Lifestyle Care (organic vegetables)
Participants will start at a 3 mg dose of OS. If this minimum dose is not tolerated, the participant will be withdrawn from the study. After 4 weeks, the OS dose will be adjusted to 7 mg. After a further 4 weeks of study and thereafter, the OS dose will be adjusted at the study physician's discretion to 14 mg. At each study visit, the current dose of OS will be maintained, unless participants report moderate-to-severe nausea or vomiting for 3 or more days in the week before the scheduled visit. If participants report moderate-to-severe nausea or vomiting, the OS dose will be maintained or decreased at the study physician's discretion. Participants will be instructed to swallow the OS tablet whole (not crushed, cut or chewed) in the morning, in a fasted state, with up to 120 mL of plain water, at least 30 minutes before any other food, beverage, or oral medication. |
All participants will start at a 3 mg dose of OS or matched Placebo.
If this minimum dose is not tolerated, the participant will be withdrawn from the study.
After 4 weeks, the OS dose (or Placebo) will be adjusted to 7 mg.
After a further 4 weeks of study and thereafter, the OS dose (or Placebo) will be adjusted at the study physician's discretion to 14 mg.
At each study visit, the current dose of OS (or Placebo) will be maintained, unless participants report moderate-to-severe nausea or vomiting for 3 or more days in the week before the scheduled visit.
Other Names:
Prescriptions of organic vegetables
|
Placebo Comparator: Oral Semaglutide (OS) Placebo with Enhanced Lifestyle Care (organic vegetables)
Participants will start at a 3 mg dose of OS matched Placebo. If this minimum dose is not tolerated, the participant will be withdrawn from the study. After 4 weeks, the Placebo will be adjusted to 7 mg. After a further 4 weeks of study and thereafter, the Placebo will be adjusted at the study physician's discretion to 14 mg. At each study visit, the current dose of Placebo will be maintained, unless participants report moderate-to-severe nausea or vomiting for 3 or more days in the week before the scheduled visit. If participants report moderate-to-severe nausea or vomiting, the Placebo will be maintained or decreased at the study physician's discretion. Participants will be instructed to swallow the matched OS Placebo whole (not crushed, cut or chewed) in the morning, in a fasted state, with up to 120 mL of plain water, at least 30 minutes before any other food, beverage, or oral medication. |
Prescriptions of organic vegetables
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
HbA1c < 7.0%
Time Frame: At 50 weeks
|
proportion of participants achieving an HbA1c < 7.0% at 50 weeks post-baseline in both groups (OS versus Placebo) with both groups receiving enhanced lifestyle care.
|
At 50 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
HbA1c
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
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At 50 weeks
|
Weight
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Waist circumference
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Lying and standing blood pressure
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Fasting glucose levels
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Fasting insulin levels
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Calculation of insulin resistance (HOMA-B and HOMA-IR)
Time Frame: At 50 weeks
|
Comparison with baseline (-2 weeks)
|
At 50 weeks
|
Lipid Levels
Time Frame: Comparison with baseline (-2 weeks) and at 50 weeks
|
Lipid levels- (total cholesterol, HDL-cholesterol, LDL-cholesterol and triglycerides)
|
Comparison with baseline (-2 weeks) and at 50 weeks
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Liver Function Test
Time Frame: Comparison with baseline (-2 weeks) and at 50 weeks
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Liver Function Test (AST, ALT, Albumin)
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Comparison with baseline (-2 weeks) and at 50 weeks
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CGM Time In Range
Time Frame: Weeks 48-49
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Comparison of Continuous Glucose Monitoring data collected over weeks 48-49 with baseline of time in range (70-180 mg/dl) using continuous glucose monitoring
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Weeks 48-49
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Number of Pill Counts
Time Frame: Comparison at 4, 8, 22, 34, and 48 weeks
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Adherence to prescribed medicines- Number of Pill Counts
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Comparison at 4, 8, 22, 34, and 48 weeks
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Additional glucose-lowering medication (rescue medication)
Time Frame: Comparison at 4, 8, 22, 34, and 48 weeks
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The need for additional glucose-lowering medication (rescue medication) initiated by the study physician with recording of additional medication by medication name
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Comparison at 4, 8, 22, 34, and 48 weeks
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Number of participants with treatment-related adverse events assessed by research physician classified according to Good Clinical Practice guidelines
Time Frame: Data captured at baseline
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Participants unable to tolerate the treatment medication
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Data captured at baseline
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: David Kerr, MD, Sansum Diabetes Research Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- U1111-1238-3149
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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