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Completed

NCT Number: NCT05160272

Effects of GABAA Receptor Modulation by AP-325 on Insulin Secretion in Patients with Type 2 Diabetes

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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Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

German Diabetes Center

Düsseldorf, North Rhine-Westphalia, 40225, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of T2D
  • Age between 25 and 75 years
  • HbA1c ≥6.5 and ≤9.5 %
  • BMI ≤ 45 kg/m2
  • Treatment-naive or stable antihyperglycemic therapy with metformin, α-glucosidase-inhibitor and/or SGLT2 inhibitor
  • Ability to give consent

Exclusion criteria

  • Acute infections (hsCRP > 5mg/dl, body temperature >37.5°C)
  • Insulin therapy or treatment with sulfonylureas, glinides, GLP-1 receptor agonists, thiazolidinediones; current treatment with DPP-4 inhibitors or during the 4 weeks prior to baseline examination
  • Uncontrolled hyperglycemia, e.g. fasting blood glucose >240 mg/dl
  • Heart rate <50 or >100 beats per minute; systolic blood pressure <100 or >160 mmHg; diastolic blood pressure <50 or >100 mmHg; uncontrolled hypertension
  • Creatinine clearance <60 ml/min (eGFR by MDRD formula)
  • Severe chronic illnesses, such as congestive heart failure (NYHA III/IV), liver insufficiency (Child-Pugh Class B/C), history of acute coronary syndrome, stroke
  • Anemia (Hb <12 g/l for men, Hb <11 g/l for women)
  • Participation in another intervention study within 2 months before the examination
  • Hypersensitivity against AP-325, placebo or other ingredients of IMP
  • Immunocompromising diseases
  • Immunomodulatory drugs (e.g. oral cortisone preparations, biologicals)
  • Thyroid diseases with an unstable metabolic state (change in L-thyroxine dose within the past 6 weeks, TSH and fT4 outside the normal range)
  • Planned pregnancy, pregnant or lactating women, positive pregnancy test, and woman of childbearing potential not using two adequate methods of contraception, including a barrier method and a highly efficacious non-barrier method
  • Past (≤ 5 years) or current history of psychiatric disorders, including psychiatric depression
  • HIV, hepatitis B or C disease
  • Previous / current alcohol and / or drug abuse
  • Malignant cancer
  • BIA and MR-incompatible metal or magnetic implants, devices or objects inside of or on the body, claustrophobia
  • Treatment with the following drug groups or agents:

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

  • Inhibitors or inducers of CYP2C9, CYP3A4, such as amiodarone, verapamil, rifampicin
  • Poor CYP2C9 metabolizer

Treatment and study plan

AP-325

Drug

Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment.

Placebo matching AP-325

Drug

Measurement of the effect of AP-325 50mg/d compared to matching placebo after 4-week treatment.

Primary outcomes

  1. Circulating C-peptide by iAUC of C-peptide during an IVGTT

    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

Secondary outcomes

  1. Basal insulin level

    Time frame: 4 weeks

    Change in basal insulin level from baseline to end of treatment

  2. C-peptide level

    Time frame: 4 weeks

    Change in C-peptide level from baseline to end of treatment

  3. Glucose level

    Time frame: 4 weeks

    Change in glucose level from baseline to end of treatment

  4. iAUC of circulating insulin (overall)

    Time frame: 4 weeks

    Change in iAUC of circulating insulin during an IVGTT from baseline to end of treatment

  5. iAUC of C-peptide level (overall)

    Time frame: 4 weeks

    Change in C-peptide level during an IVGTT from baseline to end of treatment

  6. iAUC of glucose level (overall)

    Time frame: 4 weeks

    Change in iAUC of glucose level during an IVGTT from baseline to end of treatment

  7. iAUC of circulating insulin (AIR) (first 10 min)

    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

  8. iAUC of C-peptide (first 10 min)

    Time frame: 4 weeks

    Change in iAUC of C-peptide during an IVGTT in the first 10 minutes from baseline to end of treatment

  9. iAUC of glucose (first 10 min)

    Time frame: 4 weeks

    Change in iAUC of glucose during an IVGTT in the first 10 minutes from baseline to end of treatment

  10. disposition index (DI)

    Time frame: 4 weeks

    Change in the disposition index (DI) through Minimal Model during an IVGTT from baseline to end of treatment

  11. peak insulin response

    Time frame: 4 weeks

    Change in peak insulin response during an IVGTT from baseline to end of treatment

  12. insulin secretion rate (ISR)

    Time frame: 4 weeks

    Change in insulin secretion rate (ISR) during an IVGTT from baseline to end of treatment

  13. fructosamine levels

    Time frame: 4 weeks

    Change in 1.5-Anhydroglucitol glucose from baseline to end of treatment

  14. fructosamine levels II

    Time frame: 4 weeks

    Change in fructosamine level from baseline to end of treatment

  15. fructosamine levels III

    Time frame: 4 weeks

    Change in fasting blood glucose from baseline to end of treatment

  16. Plasma concentrations of AP-325

    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

  17. Ctrough-ss (Day 28) and the change from baseline 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

Sponsors and collaborators

Lead sponsor

The Deutsche Diabetes Forschungsgesellschaft e.V.

Other

Collaborators

  • Algiax Pharmaceuticals GmbH

Registry information

Official study title

Effects of GABAA Receptor Modulation by AP-325 on Insulin

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Dec 16, 2021
Registry last updated
Jan 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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