Dapansutrile in Diabetes and Diabetes-Related Complications - Dapan-Dia
Study Details
Study Description
Brief Summary
The aim of the study is to determine whether NLRP3 inhibition with dapansutrile represents a new pharmacological option for diabetes management with potential as an anti-inflammatory agent to also address micro- and macro-vascular risk and complications from diabetes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
To date, no other oral NLRP3 inhibitor has sufficiently advanced in development to be tested in a chronic low-grade inflammatory disease such as type 2 diabetes mellitus over a period of 3 to 4 months as proposed in this trial. Based on the publicly available information, dapansutrile is the most advanced oral NLRP3 inhibitor in development. The rationale is built upon dapansutrile's clinical and extensive preclinical and safety findings, and from data in chronic animal toxicology studies to date, which together enable and support its investigation in select chronic low-grade inflammatory diseases. Therefore, the investigators have selected type 2 diabetes mellitus and its complications, including risk for cardiovascular disease, as a disease with clinical features of low-grade inflammation to further investigate the therapeutic potential of NLRP3 inhibition with dapansutrile.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Intervention Group 1000 mg dapansutrile (2 × 500mg tablets) administered twice a day from day 1 through the week 26 visit, inclusive. All tablets will be self-administered by mouth with water, with or without food. |
Drug: Dapansutrile
Patients receive investigational product.
Other Names:
|
| Placebo Comparator: Control Group Matching placebo (2 tablets) administered twice a day from day 1 through the Week 26 visit, inclusive. All tablets will be self-administered by mouth with water, with or without food. |
Drug: Placebo
Patients receive placebo.
|
Outcome Measures
Primary Outcome Measures
- Change in HbA1c in blood of patients for dapansutrile compared to placebo [two time assessment at baseline and week 26]
Comparison of change in HbA1c for dapansutrile and placebo
Secondary Outcome Measures
- Change in HbA1c in blood of patients for dapansutrile compared to placebo [six time assessment at baseline and week 4, 8, 12, 16, 20]
Comparison of change in HbA1c for dapansutrile and placebo
- Change in fasting plasma glucose for dapansutrile compared to placebo [seven time assessement at baseline and week 4, 8, 12, 16, 20, 26]
Comparison of change in fasting plasma glucose for dapansutrile and placebo
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Diagnosis of type 2, Diabetes mellitus as defined by the criteria of the American Diabetes Association (ADA) Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (see Appendix 1) and recognized by the World Health Organization (WHO, 2019), for at least 3 months prior to the Baseline Visit/Day 1
-
HbA1c value of ≥ 7.7% to ≤ 11.0% at the Screening Visit.
-
High-sensitivity C-reactive protein (hsCRP) ≥ 1.5 mg/L at the Screening Visit.
-
Body mass index (BMI) ≥18 to ≤ 40 kg/m2 at the Screening Visit
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Acceptable overall medical condition to safely participate in the study and complete all study procedures (particularly with regard to cardiovascular, renal, and hepatic conditions), in the opinion of the Investigator
Exclusion Criteria:
-
Diagnosis of type 1 diabetes mellitus
-
HbA1c value of ≤ 7.5% or ≥ 10.5% at the Baseline Visit/Day 1, as determined at point of care (local laboratory)
-
Use of thiazolidinediones (glitazones), pramlintide, or short-acting insulin/insulin analogues (as bolus or premixed insulin) within 12 weeks prior to the Screening Visit
-
Less than 80% compliance in taking investigational medicinal product (placebo tablets) by pill count during the Single-Blind Run-In Period, as assessed at the Baseline Visit/Day 1
-
Significant weight loss (> 5 kg) in the 12 weeks prior to the Screening Visit
-
Systolic blood pressure (BP) ≥ 160 mmHg, diastolic BP ≥ 100 mmHg, or resting heart rate (HR) ≥ 100 beats/minute at the Screening Visit
-
Previous myocardial infarction, any cardiac surgery
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Hospital Basel | Basel | Switzerland | 4031 |
Sponsors and Collaborators
- University Hospital, Basel, Switzerland
- European Union (Horizon Europe Programme)
- State Secretariat for Education Research and Innovation, Switzerland
- Olatec Therapeutics LLC
Investigators
- Principal Investigator: Marc Y. Donath, Prof., University Hospital, Basel, Switzerland
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2023-01387; kt23Donath3