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| Name | Class |
|---|---|
| Bukwang Pharmaceutical, Co., Ltd. | INDUSTRY |
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A Multi-center, Double Blind, Randomized, Placebo-controlled, Parallel Group Phase IIa Study of MLR-1023 in Adult Subjects With Uncontrolled Type 2 Diabetes
Objectives
Design and Outcomes
The study is a randomized, double blind, placebo-controlled, parallel group study of MLR-1023 in adult subjects with uncontrolled type 2 diabetes mellitus who are on diet and exercise therapy.
A subset of subjects per dose group will have additional samples analyzed to measure signs of MLR-1023.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator |
| |
| 100 mg q.d. | Active Comparator |
| |
| 100 mg b.i.d. | Active Comparator |
| |
| 200 mg q.d. | Active Comparator |
| |
| 200 mg b.i.d. | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MLR-1023 | Drug | Each subject will receive an oral dose of placebo or MLR-1023 once before breakfast and either placebo (placebo and q.d. dose groups) or a second dose of MLR-1023 (b.i.d. dose groups) before dinner for 4 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in PPG AUC0-3h in a MMTT between Days 1 and 29. | 29 Days |
| Measure | Description | Time Frame |
|---|---|---|
| Change in fasting plasma glucose in dose groups from Day 1 to Day 29, Day 36 | 36 Days | |
| Change in fructosamine level from Day 1 to Day 29 | 29 Days | |
| Change in fasting insulin from Day 1 to Day 29 |
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Inclusion Criteria:
Exclusion Criteria:
History of Type 1 diabetes
History of more than 1 episode of severe hypoglycemia within 6 months prior to screening, or a current diagnosis of hypoglycemia unawareness.
Hospitalizations or Emergency room visits that would impact patient safety or data interpretation:
Significant change of body weight (>10%) in the 3 months before screening
Proliferative retinopathy or maculopathy within the 6 months before screening or requiring acute treatment, or severe neuropathy
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| Name | Affiliation | Role |
|---|---|---|
| Melior Pharmaceuticals I & Bukwang Pharm. Co., Ltd. | Melior Pharmaceuticals I & Bukwang Pharm. Co., Ltd. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Melior Pharmaceuticals I & Bukwang Pharm. Co., Ltd. | USA and South Korea | Pennsylvania | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32019723 | Derived | Lee MK, Kim SG, Watkins E, Moon MK, Rhee SY, Frias JP, Chung CH, Lee SH, Block B, Cha BS, Park HK, Kim BJ, Greenway F. A novel non-PPARgamma insulin sensitizer: MLR-1023 clinicalproof-of-concept in type 2 diabetes mellitus. J Diabetes Complications. 2020 May;34(5):107555. doi: 10.1016/j.jdiacomp.2020.107555. Epub 2020 Feb 2. |
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| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| C576397 | 5-(3-methylphenoxy)-2(1H)-pyrimidinone |
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| 29 Days |
| Change in glycated albumin from Day 1 to Day 29 | 29 Days |
| Change from Day 1 to Day 29 in insulin sensitivity using HOMA-R (HOMA-R = fasting plasma insulin (mU/l) * fasting plasma glucose (mmol/l) / 22.5) | 29 Days |
| Changes from Day 1 to Day 29 in beta-cell function using HOMA-B (HOMA-B = 20 * fast- ing plasma insulin (mU/l) / [fasting plasma glucose (mmol/l) - 3.5]) | 29 Days |
| Change in HbA1C between Days 1 and Day 29 | 29 Days |
| Changes in LDL-C, HDL-C, TG between Days 1 and Day 29 | 29 Days |
| Change in weight between Days 1 and Day 29 | 29 Days |
| Differences between placebo and MLR-1023 dose groups in PPG AUC0-3h Days 1 and 29. | 29 Days |
| D004700 | Endocrine System Diseases |