Condition: Diabetes Mellitus, Type 2 · Sponsor: Merck Sharp & Dohme LLC
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
The purpose of this study is to learn about the safety and if people tolerate a study medicine called MK-2828. The study will also measure what happens to MK-2828 in the body of a person with type 2 diabetes (T2D) over time (pharmacokinetic or PK study), and how it affects the amount of high-sensitivity C-reactive protein (hsCRP) in a person's blood.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: The main inclusion criteria include but are not limited to the following: * With the exception of type 2 diabetes mellitus (T2DM), is in generally good health * Has a history of T2DM for ≥1 year at the time of screening based on self-reporting * Has a baseline HbA1C level of ≤10% at the time of screening * Has a stable weight (based on self-reporting) defined as ≤5 kg gain or loss of body weight for at least 3 months before Visit 1/Screening * T2DM treated with lifestyle modification alone or with stable doses (no significant change for ≥3 months from Visit 1/Screening, based on self-reporting) of ≤ 3 oral anti-diabetic medications and anticipated not to require dose adjustments during the study duration * Body mass index (BMI) between 25 and 40 kg/m2, inclusive Exclusion Criteria: The main exclusion criteria include but are not limited to the following: * Has known systemic hypersensitivity to the MK-2828 drug substance or other nucleotide-binding, leucine-rich, protein 3 inhibitor (NLRP3i) based therapy, its inactive ingredients, or the placebo * Has a history of congestive heart failure (New York Heart Association \[NYHA\] Class 3 or 4) * Has a history of myocardial infarction, uncontrolled arrhythmias, cardiac revascularization, unstable peripheral arterial disease and/or stroke within 6 months of screening * History of significant multiple and/or severe allergies (e.g., food, drug, latex allergy), or has had an anaphylactic reaction or significant intolerability (i.e., systemic allergic reaction) to prescription or nonprescription drugs or food * Has type 1 diabetes mellitus or secondary types of diabetes * Has experienced complications of diabetes such as ketoacidosis, unstable diabetic retinopathy, or maculopathy * Has previous or planned (during the trial period) obesity treatment with surgery or a weight loss device
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| ProSciento Inc. ( Site 0004) | Chula Vista, California, United States | — |
| California Clinical Trials Medical Group managed by PAREXEL ( Site 0008) | Glendale, California, United States | — |
| Velocity Clinical Research, Hallandale Beach ( Site 0010) | Hallandale, Florida, United States | — |
| Jacksonville Center for Clinical Research ( Site 0002) | Jacksonville, Florida, United States | — |
| Advanced Pharma CR, LLC ( Site 0001) | Miami, Florida, United States | — |
| QPS Miami Research Associates ( Site 0005) | South Miami, Florida, United States | — |
| AMR Lexington ( Site 0012) | Lexington, Kentucky, United States | — |
| Alliance for Multispecialty Research, LLC ( Site 0013) | Kansas City, Missouri, United States | — |
| Bio-Kinetic Clinical Applications, LLC dba QPS-MO ( Site 0009) | Springfield, Missouri, United States | — |
| AMR Clinical ( Site 0003) | Knoxville, Tennessee, United States | — |
| ICON Early Phase Services ( Site 0006) | San Antonio, Texas, United States | — |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.