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This study is designed as a prospective, multi-centre, parallel group, double-blind randomized, placebo-controlled, phase 3 clinical study to evaluate the efficacy and safety of MP-513 (Teneligliptin) in combination with metformin.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Teneligliptin 20mg | Experimental | Teneligliptin (20mg once daily) for 24 weeks in combination with metformin |
|
| Placebo | Placebo Comparator | Placebo for 24 weeks in combination with metformin |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Teneligliptin 20mg | Drug |
| ||
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| The Changes in HbA1c at Week 24 | The change in HbA1c from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS. | at Day 1(baseline) and Week 24 |
| Measure | Description | Time Frame |
|---|---|---|
| The Changes in Fasting Plasma Glucose (FPG) at Week 24 | The change in FPG from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS. | at Day 1(baseline) and Week 24 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| General Manager | Tanabe Pharma Corporation | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Investigational center | Beijing | China |
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| ID | Title | Description |
|---|---|---|
| FG000 | Teneligliptin 20mg + Metformin | Teneligliptin (20 mg once daily) for 24 weeks in combination with metformin. |
| FG001 | Placebo + Metformin | Placebo for 24 weeks in combination with metformin. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
FAS: All subjects in the randomized set who have received at least one dose of study medication during the double-blind treatment period and have at least one post-baseline efficacy observation. Subjects who were not diagnosed with type 2 diabetes mellitus were excluded.
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| ID | Title | Description |
|---|---|---|
| BG000 | Teneligliptin 20mg + Metformin | Teneligliptin (20 mg once daily) for 24 weeks in combination with metformin. |
| BG001 | Placebo + Metformin | Placebo for 24 weeks in combination with metformin. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | The Changes in HbA1c at Week 24 | The change in HbA1c from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS. | All subjects in the randomized set who have received at least one dose of study medication during the double-blind treatment period and have at least one post-baseline efficacy observation. Subjects who were not diagnosed with type 2 diabetes mellitus were excluded. | Posted | Least Squares Mean | Standard Error | percentage of HbA1c | at Day 1(baseline) and Week 24 |
|
24 weeks
All subjects in the randomized set who have received at least one dose of study medication during the double-blind treatment period. One subject who had been randomized in placebo group was handled as Teneligliptin group, because the subject had been administered Teneligliptin mistakenly.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Teneligliptin 20mg + Metformin | Teneligliptin (20 mg once daily) for 24 weeks in combination with metformin. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Arrhythmia | Cardiac disorders | MedDRA 21.0 | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Upper respiratory tract infection | Infections and infestations | MedDRA 21.0 | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Clinical Trials, Information Desk | Tanabe Pharma Corporation | Please e-mail | cti-inq-ml.JP@ml.tanabe-pharma.com |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Apr 29, 2016 | Nov 15, 2021 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Dec 11, 2018 | Nov 15, 2021 | SAP_001.pdf |
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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 |
|---|---|
| C579035 | 3-(4-(4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl)pyrrolidin-2-ylcarbonyl)thiazolidine |
| D008687 | Metformin |
| ID | Term |
|---|---|
| D001645 | Biguanides |
| D006146 | Guanidines |
| D000578 | Amidines |
| D009930 | Organic Chemicals |
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|
| Metformin ≥ 1000 mg | Drug |
|
| Physician Decision |
|
| Protocol Violation |
|
| Withdrawal by Subject |
|
| Other |
|
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
Placebo for 24 weeks in combination with metformin.
|
|
| Secondary | The Changes in Fasting Plasma Glucose (FPG) at Week 24 | The change in FPG from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS. | All subjects in the randomized set who have received at least one dose of study medication during the double-blind treatment period and have at least one post-baseline efficacy observation. Subjects who were not diagnosed with type 2 diabetes mellitus were excluded. | Posted | Least Squares Mean | Standard Error | mg/dL | at Day 1(baseline) and Week 24 |
|
|
|
| 0 |
| 124 |
| 4 |
| 124 |
| 35 |
| 124 |
| EG001 | Placebo + Metformin | Placebo for 24 weeks in combination with metformin. | 0 | 123 | 6 | 123 | 43 | 123 |
| Sinus node dysfunction | Cardiac disorders | MedDRA 21.0 | Systematic Assessment |
|
| Cataract | Eye disorders | MedDRA 21.0 | Systematic Assessment |
|
| Gastric polyps | Gastrointestinal disorders | MedDRA 21.0 | Systematic Assessment |
|
| Ligament sprain | Injury, poisoning and procedural complications | MedDRA 21.0 | Systematic Assessment |
|
| Subarachnoid haemorrhage | Injury, poisoning and procedural complications | MedDRA 21.0 | Systematic Assessment |
|
| Intervertebral disc protrusion | Musculoskeletal and connective tissue disorders | MedDRA 21.0 | Systematic Assessment |
|
| Osteoarthropathy | Musculoskeletal and connective tissue disorders | MedDRA 21.0 | Systematic Assessment |
|
| Cerebral infarction | Nervous system disorders | MedDRA 21.0 | Systematic Assessment |
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| Hypertension | Vascular disorders | MedDRA 21.0 | Systematic Assessment |
|
| Hyperlipidaemia | Metabolism and nutrition disorders | MedDRA 21.0 | Systematic Assessment |
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| Hyperuricaemia | Metabolism and nutrition disorders | MedDRA 21.0 | Systematic Assessment |
|
| Proteinuria | Renal and urinary disorders | MedDRA 21.0 | Systematic Assessment |
|
| Hypertension | Vascular disorders | MedDRA 21.0 | Systematic Assessment |
|
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| D004700 | Endocrine System Diseases |