Phase IIa Trial to Determine the Effects of Bardoxolone Methyl on Renal Function in Patients With Diabetic Nephropathy

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

To determine the effects of three different doses of bardoxolone methyl administered orally on the kidney function (glomular filtration rate) in patients with diabetic nephropathy.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Reata Pharmaceuticals, Inc.

Criteria

Inclusion Criteria:

1. Diagnosis of type 2 diabetes;

2. Serum creatinine in women 1.3 - 3.0 mg/dL (115-265 μmol/L), inclusive, and in men 1.5

• 3.0 mg/dL (133-265 μmol/L), inclusive;

3. Patient must agree to practice effective contraception.

4. Patient must have a negative urine pregnancy test within 72 hours prior to the first dose of study medication.

5. Patient is willing and able to cooperate with all aspects of the protocol and is able to communicate effectively.

6. Patient is willing and able to provide written informed consent to participate in this clinical study.

Exclusion Criteria:

1. Type 1 (insulin-dependent; juvenile onset) diabetes.

2. Patients with known non-diabetic renal disease (nephrosclerosis superimposed on diabetic nephropathy acceptable), or with renal allograft.

3. Cardiovascular disease as follows: unstable angina pectoris within 3 mo of study entry; myocardial infarction, coronary artery bypass graft surgery, or percutaneous transluminal coronary angioplasty/stent within 3 mo of study entry; transient ischemic attack within 3 mo of study entry; cerebrovascular accident within 3 mo of study entry; obstructive valvular heart disease or hypertrophic cardiomyopathy; second or third degree atrioventricular block not successfully treated with a pacemaker.

4. Need for chronic (>2 weeks) immunosuppressive therapy, including corticosteroids (excluding inhaled or nasal steroids) within 3 mo of study entry.

5. Evidence of hepatic dysfunction including total bilirubin >1.5 mg/dL (>26 micromole/L); elevation of liver transaminase (aspartate aminotransferase [AST] or alanine transferase [ALT])above the upper limit of normal(ULN) within the 14-day screening period; documented elevation (above ULN) of AST or ALT within 3 months prior to screening; elevation of alkaline phosphatase (ALP) above 1.5 x ULN; documented elevation of gamma-glutamyl transpeptidase (GGT) above 1.5 X ULN.

6. If female, patient is pregnant, nursing or planning a pregnancy.

7. Patient has any concurrent clinical conditions that in the judgment of the investigator could either potentially pose a health risk to the patient while involved in the study or could potentially influence the study outcome;

8. Patient has known hypersensitivity to any component of the study drug;

9. Patient has known allergy to iodine;

10. Patient has undergone diagnostic or intervention procedure requiring a contrast agent within the last 30 days prior to entry into the study;

11. Change or dose-adjustment in any of the following medications: ACE inhibitors, angiotensin II blockers, non-steroidal anti inflammatory drugs (NSAIDs), or COX-2 inhibitors within 3 months; other anti-hypertensive, and other anti-diabetic medications within 6 weeks prior to entry into the study;

12. Patient has a history of drug or alcohol abuse or has positive test results for any drug of abuse (positive urine drug test and/or alcohol breathalyzer test).

13. Patients who are unable or unwilling to discontinue the following medications until 1 week following last dose of study treatment: Nicotinic acid, Isoniazid, Dantrolene, Labetalol, Pemoline, Felbamate, Zileutan, Tolcapone, Trovafloxacin, Vitamin D, Vitamin D analogues (such as Calcitriol, paricalcitol, doxercalciferol), or multivitamins containing vitamin D or related analogs, or Fenofibrate. Patient must have been off the aforementioned medications for a minimum of two weeks prior to enrollment.

14. Patient with an intact parathyroid hormone (iPTH) level > 300 pg/mL.

15. Patient has participated in another clinical study involving investigational or marketed products within 30 days prior to entry into the study or would concomitantly participate in such a study.

16. Patient is unable to communicate or cooperate with the Investigator due to language problems, poor mental development or impaired cerebral function.