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| Name | Class |
|---|---|
| Algiax Pharmaceuticals GmbH | INDUSTRY |
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The aim of this single-center, prospective, randomized, double-blind, placebo-controlled, 2-arm parallel-group interventional study is to investigate the effect of 4-week treatment with AP-325 on C-peptide release as measure of insulin secretion compared to placebo in type 2 diabetes (T2D) patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AP-325 Treatment | Experimental | AP-325, film-coated tablet, 50mg once daily |
|
| Placebo Treatment | Placebo Comparator | Placebo matching AP-325 film-coated tablet, once daily |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AP-325 | Drug | Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Circulating C-peptide by iAUC of C-peptide during an IVGTT | Change in circulating C-peptide levels from baseline to end of intervention measured by iAUC of C-peptide during an IVGTT until 60th minute (second phase) with AP-325 compared to placebo | 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Basal insulin level | Change in basal insulin level from baseline to end of treatment | 4 weeks |
| C-peptide level | Change in C-peptide level from baseline to end of treatment |
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Inclusion Criteria:
Exclusion Criteria:
Anticoagulant drugs (exception: acetylsalicylic acid 100 mg/day), dihydropyridines (e.g. nifedipine, amlodipine), azilsartan, losartan and irbesartan, celecoxib; if applicable, other drugs that are predominantly metabolized by CYP2C9
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| Name | Affiliation | Role |
|---|---|---|
| Michael Roden, MD | Deutsches Diabetes-Zentrum | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| German Diabetes Center | Düsseldorf | North Rhine-Westphalia | 40225 | Germany |
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| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| D003920 | Diabetes Mellitus |
| ID | Term |
|---|---|
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
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| Placebo matching AP-325 | Drug | Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment. |
|
| 4 weeks |
| Glucose level | Change in glucose level from baseline to end of treatment | 4 weeks |
| iAUC of circulating insulin (overall) | Change in iAUC of circulating insulin during an IVGTT from baseline to end of treatment | 4 weeks |
| iAUC of C-peptide level (overall) | Change in C-peptide level during an IVGTT from baseline to end of treatment | 4 weeks |
| iAUC of glucose level (overall) | Change in iAUC of glucose level during an IVGTT from baseline to end of treatment | 4 weeks |
| iAUC of circulating insulin (AIR) (first 10 min) | Change in iAUC of circulating insulin (AIR) during an IVGTT in the first 10 minutes from baseline to end of treatment | 4 weeks |
| iAUC of C-peptide (first 10 min) | Change in iAUC of C-peptide during an IVGTT in the first 10 minutes from baseline to end of treatment | 4 weeks |
| iAUC of glucose (first 10 min) | Change in iAUC of glucose during an IVGTT in the first 10 minutes from baseline to end of treatment | 4 weeks |
| disposition index (DI) | Change in the disposition index (DI) through Minimal Model during an IVGTT from baseline to end of treatment | 4 weeks |
| peak insulin response | Change in peak insulin response during an IVGTT from baseline to end of treatment | 4 weeks |
| insulin secretion rate (ISR) | Change in insulin secretion rate (ISR) during an IVGTT from baseline to end of treatment | 4 weeks |
| fructosamine levels | Change in 1.5-Anhydroglucitol glucose from baseline to end of treatment | 4 weeks |
| fructosamine levels II | Change in fructosamine level from baseline to end of treatment | 4 weeks |
| fructosamine levels III | Change in fasting blood glucose from baseline to end of treatment | 4 weeks |
| Plasma concentrations of AP-325 | Change in Plasma concentrations of AP-325 at 1 hour post-dose on Days 1 and 28; pre-dose on Days 4 and 28. Accumulation of Ctrough from Day 4 to Day 28 | 4 weeks |
| Ctrough-ss (Day 28) and the change from baseline to Day 28 | Change in relationship between Ctrough-ss (Day 28) and the change from baseline to Day 28 in primary and secondary endpoints | 4 weeks |