Safety Study of GE-145 320 mg I/mL Injection vs. Iopamidol 370 mg I/mL in Elderly Subjects Undergoing Coronary Procedure
| Status: | Completed |
|---|---|
| Conditions: | Renal Impairment / Chronic Kidney Disease, Cardiology, Diabetes |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Endocrinology, Nephrology / Urology |
| Healthy: | No |
| Age Range: | 65 - Any |
| Updated: | 8/31/2018 |
| Start Date: | November 2010 |
| End Date: | December 2012 |
A Phase 2, Double-Blind, Randomized, Safety Study of GE-145 320 mg I/mL Injection Versus Iopamidol 370 mg I/mL in Elderly Subjects Undergoing Coronary Artery Catheterization Procedure
To evaluate cardio-renal and overall safety profile of GE 145 320 mg I/ml Injection when
compared to iopamidol 370 mg I/mL. The study will focus on elderly subjects with either
chronic renal insufficiency, or diabetes mellitus (DM) requiring drug therapy, or congestive
heart failure (CHF) NYHA Class III or greater, who are referred for a coronary
catheterization procedure with or without PCI.
compared to iopamidol 370 mg I/mL. The study will focus on elderly subjects with either
chronic renal insufficiency, or diabetes mellitus (DM) requiring drug therapy, or congestive
heart failure (CHF) NYHA Class III or greater, who are referred for a coronary
catheterization procedure with or without PCI.
Inclusion Criteria:
- Males and females 65 years of age with cardiovascular disease who are referred for a
coronary catheterization procedure with or without PCI.
- The subject has at least one of the following comorbidities:
- 1) Chronic renal insufficiency, (eGFR <60 but 15 mL/min/1.73 m2 according to the MDRD
equation) as measured within 2 weeks or at the screening visit;
- 2) DM diagnosed greater than 6 months prior to study entry and which requires either
insulin or anti-hyperglycemic drug therapy;
- 3) CHF (NYHA) class III or greater measured within 2 weeks of enrollment or at the
screening visit.
Exclusion Criteria:
- The subject has known allergies to either iodine or any ICM.
- The subject has severe renal insufficiency (eGFR <15 mL/min/1.73 m2 according to the
MDRD equation) or is on dialysis.
- The subject has acute coronary syndrome requiring emergency coronary angiography
and/or intervention.
- The subject is not willing or unable to discontinue metformin (e.g., Glucophage) at
the time of the study procedure.
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