Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:54 PM
Ignite Modification Date:
2025-12-24 @ 6:54 PM
NCT ID:
NCT03686657
Eligibility Criteria:
Inclusion Criteria:
1. Males and females, Age: \>18 to 70 years at the time of screening visit.
2. Women of childbearing potential (WOCBP) must have negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent of HCG) within 24 hours prior to the start of the study.
3. Women must not be breastfeeding.
4. HbA1c≥8.0
5. Patients with inadequate blood glucose control with Metformin defined as a central laboratory glycosylated hemoglobin (HbA1c) \>8.0 and \<10.5 obtained at the screening visit. Metformin-HCl monotherapy was inadequate 3 months prior to the study as indicated by the lack of decrease and/or an increase in the A1c level.
Newly diagnosed drug naïve patients as defined by HbA1c\>7.0 at the screening visit. Drug naïve subjects diagnosed with type 2 diabetes within 6 months of diagnosis will be considered and selected.
About half the patients are expected to be newly diagnosed in the study.
6. Drug naive as well as osteoarthritis patients with Type 2 diabetes receiving a non-aspirin pain reliever (e.g. acetaminophen) or an NSAID (e.g. Naproxen).
7. Max/maintenance dose Metformin. Subjects should have been taking the same daily dose of metformin for at least 8 weeks prior to the enrollment visit and subjects not receive these other antihyperglycemic medications within the 12 weeks prior to screening (except for short-term use of insulin \[≤7 days\] during concomitant illness or other stress).
8. Patients with \>25% AIRg at 2 minutes and 10 minutes.
9. RAS blocker naïve patients
10. 2-Hour OGTT ≥200 mg/dL
11. FPG ≥140 mg/dL
12. BMI ≥30
13. Impaired first phase and second phase of insulin secretion
14. BP ≥140/90 mm Hg (These patients might be on an anti-hypertensive drug)
15. Non-fasting laboratory glucose \>200 mg/dL with symptoms of polydipsia, polyuria and/or Polyphagia
16. eGFR ≥ 60 ml/min/1.73m2
Exclusion Criteria:
1. Age \>70
2. Patients with Type 1 diabetes, Screen for GAD (Glutamic acid decarboxylase) antibodies at the time of screening visit. To rule out latent autoimmune diabetes in adults (LADA), screening for other diabetes-related antibodies, such as insulinoma-associated protein (IA-2 and IA-2 beta), zinc transporter-8 (ZnT8), islet cell antibodies (ICA) or insulin autoantibody (IAA) will also be considered.
3. Pregnant women
4. Patients with a history of Ketoacidosis.
5. Subjects at serious risk of gastrointestinal (GI) adverse events (e.g. current or recent history of GI bleeding ulceration, or perforation).
6. Subjects with a planned radiologic study with intravenous contrast, surgery, or other planned procedures that may predispose them to metformin-associated lactic acidosis.
7. Insulin dependent: \<25% Beta-cell function: AIRg (Acute insulin response to glucose after 2 min and 10 min after glucose injection) INSULIN DEPENDENT STATE.
8. Patients with a history of uncontrolled hyperglycemia \>15.0 mmol/L (280 mg/dL) after an overnight fast that required rescue therapy.
9. Patients with uncontrolled hyperglycemia \>15.0 mmol/L (280 mg/dL) after an overnight fast that required rescue therapy during week 1-3 Metformin-HCl monotherapy or RK-01 therapy.
10. eGFR, impaired kidney function \< 60 ml/min/1.73m2.
11. Poor metabolizers of Cyp450 2C9 to avoid very high concentration (Since Cytochrome 450 2C9 is responsible for the metabolism of both Valsartan and Celecoxib, patients who are known or suspected to be poor Cyp450 2C9 metabolizers based on previous history will be excluded from the study).
12. Any of the following cardiovascular (CV)/Vascular diseases within 3 months of the enrollment visit:
1. Myocardial infarction (MI)
2. Cardiac surgery or revascularization (coronary artery bypass surgery, Coronary Artery Bypass Graft \[(CABG\]/Percutaneous transluminal coronary angioplasty (PTCA)\].
3. Unstable angina
4. Unstable congestive heart failure (CHF)
5. Transient ischemic attack (TIA) or significant cerebrovascular disease
6. Unstable or previously diagnosed arrhythmia
7. Congestive heart failure, defined as New York Heart Association (NYHA) Class III and IV, unstable or acute heart failure and/or known left ventricular ejection fraction of ≤40%.
8. Acute coronary syndrome, stroke or transient ischemic attack within 3 months prior to the informed consent.
13. Previous bariatric surgery
14. Treatment with anti-obesity drugs within 3 months prior to consent
15. Patients with COPD
16. Patients with liver disease
17. Patients with renal disease
18. Patients with autoimmune diseases e.g. Lupus, Psoriasis
19. Patients with HIV/AIDS
20. Patients with diabetes-related complications
21. Patients with Hematological and Oncological Diseases/Conditions
22. Hemoglobin \<11.0 g/dL (110 g/L) for men; hemoglobin \<10.0 g/dL (100 g/L) for women
23. Patients with chronic disease e.g. Cancer, Epilepsy, Alzheimer, Parkinson, Asthma
24. Abnormal free T4
25. Patients with serious infection
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT03686657
Study Brief:
Protocol Section:
NCT03686657