German Diabetes Center
Düsseldorf, North Rhine-Westphalia, 40225, Germany
NCT Number: NCT05160272
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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Notify Me25 year–75 year
All sexes
Interventional
Phase 2
Düsseldorf, North Rhine-Westphalia, 40225, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment.
Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment.
Time frame: 4 weeks
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
Time frame: 4 weeks
Change in basal insulin level from baseline to end of treatment
Time frame: 4 weeks
Change in C-peptide level from baseline to end of treatment
Time frame: 4 weeks
Change in glucose level from baseline to end of treatment
Time frame: 4 weeks
Change in iAUC of circulating insulin during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in C-peptide level during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in iAUC of glucose level during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in iAUC of circulating insulin (AIR) during an IVGTT in the first 10 minutes from baseline to end of treatment
Time frame: 4 weeks
Change in iAUC of C-peptide during an IVGTT in the first 10 minutes from baseline to end of treatment
Time frame: 4 weeks
Change in iAUC of glucose during an IVGTT in the first 10 minutes from baseline to end of treatment
Time frame: 4 weeks
Change in the disposition index (DI) through Minimal Model during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in peak insulin response during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in insulin secretion rate (ISR) during an IVGTT from baseline to end of treatment
Time frame: 4 weeks
Change in 1.5-Anhydroglucitol glucose from baseline to end of treatment
Time frame: 4 weeks
Change in fructosamine level from baseline to end of treatment
Time frame: 4 weeks
Change in fasting blood glucose from baseline to end of treatment
Time frame: 4 weeks
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
Time frame: 4 weeks
Change in relationship between Ctrough-ss (Day 28) and the change from baseline to Day 28 in primary and secondary endpoints
The Deutsche Diabetes Forschungsgesellschaft e.V.
Other
Effects of GABAA Receptor Modulation by AP-325 on Insulin
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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