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| Other names | HOE642 |
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| Formula | C12H17N3O3S |
| Molar mass | 283.35 g·mol−1 |
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Cariporide is a selective Na+/H+ exchange inhibitor. Cariporide has been shown to actively suppress the cell death caused by oxidative stress.
Cariporide is a potent NHE1 inhibitor is may also be useful for treatment of cancer.
Mechanism of action
Cariporide targets and inhibits the Na+/H+ exchanger (NHE) isoform 1, which is ubiquitously expressed and involved in pH regulation of the myocardium. During myocardial ischemia, NHE activation leads to an influx of Na+ and, upon reperfusion, reverses the Na+/Ca2+ exchanger and results in an overload of intracellular Ca2+. By inhibiting the NHE1, cariporide limits the early influx of Na+ and lends a cardioprotective effect upon ischemia/reperfusion. Additionally, cariporide slows the normalization of cellular pH following an H+ efflux during reperfusion triggered by ischemia-induced acidosis.
It is hypothesized that cariporide may also serve as a highly selective target for anti-cancer therapy through the inhibition of NHE1 in tumor cells (see Continuing Research).
Clinical trials
Phase I
Following experimental research into NHE-activation and its effects on myocardial injury, cariporide was proposed for a Phase I trial to test whether inhibition of the NHE approves myocardial function in patients undergoing percutaneous transluminal coronary angioplasty (PCTA). Results of this trial were published in 2000. A group of 100 individuals were placed in two trial groups. The first group was given a 40-mg intravaneous bolus dose of cariporide prior to reperfusion. A second group was given a placebo. 21 days post-injection, patients in the cariporide group showed a number of improvements over the placebo group. This trial proved NHE inhibition with cariporide may be an effective way to aid recovery post-PCTA.
Phase II/Phase III: GUARDIAN trial
Acute coronary syndrome, including heart attack or unstable angina, is the number one cause of death in America. The Guard During Ischemia Against Necrosis (GUARDIAN) trial was conducted to determine whether cariporide reduced the incidence of mortality and myocardial infarction in at-risk patients. It was the first large-scale trial to determine the efficacy and safety of cariporide. The trial began in May 1997 and patients were enrolled until April 1999. A total of 382 investigative sites were chosen in 23 countries, totaling 11,590 patients. Patients were split between four study groups: placebo, 20, 80 or 120 mg doses as 60-minute infusions three times daily.
The primary goals of the GUARDIAN trial were to assess (1) the rate of death or myocardial infarction at day 36 in the four trial groups and (2) the large-scale safety and side effects associated with cariporide. Results showed that 20- and 80-mg doses were statistically similar to the placebo group, while the 120-mg group showed a 10% relative risk reduction and similar mortality rates. While cariporide showed efficacy for certain sub-groups of patients at varying drug concentrations, overall the GUARDIAN trial showed that cariporide did not significantly reduce patient risk of myocardial infarction or mortality.
Despite this result, cariporide showed promise in the post-coronary artery bypass grafting (CABG) sub-group of patients. Here, there was a 25% reduction in post-surgery mortality or MI, suggesting that high-doses and prolonged releases of cariporide may be efficacious for high-risk patients.
Phase III: EXPEDITION trial
The Sodium-Proton Exchange Inhibition to Prevent Coronary Events in Acute Cardiac Conditions (EXPEDITION) trial was a Phase III trial to assess the efficacy and safety of cariporide in patients who have received a CABG surgery. 5,761 patients were accepted from July 2001 to July 2002 and were placed in two trial groups. The first group received a consecutive dosing regimen detailed in the table below:
| Pre-Op | 180-mg, 1-hour |
| < 24h Post-Op | 40 mg/hr |
| > 24h Post-Op, < 48h Post-Op | 20 mg/hr |
The second group received a placebo. The results of the trial showed a statistically significant decline in mortality or myocardial infarction from 20.3% to 16.6%. However, when looked at individually, the rate of myocardial infarction declined from 18.9% to 14.4%, while mortality increased 0.7%. Due to the increase in mortality, cariporide did not pass clinical trials. However, these studies showed for the first time that inhibition of the NHE affords protection to the myocardium and research into decoupling its adverse effects on mortality from its protective effects is ongoing.
Dosing
In all clinical trials, cariporide was given was an intravenous injection. Early clinical trials (see Phase I) showed significant improvements over a placebo at a 40-mg dose prior to arterial surgery. Both Phase III clinical trials for cariporide conclude that it is highly dose-dependent. While earlier trials showed that high doses of cariporide (120-mg, three times daily) may increase efficacy, the EXPEDITION trial found an increased rate of mortality associated with these higher doses.
Side effects
The largest clinical trial for cariporide found no significant adverse effects of cariporide on patients (see Phase III: GUARDIAN Trial). However, a later clinical trial found dose-dependent increases in mortality for patients using cariporide post-CABG (see Phase III: EXPEDITION Trial).
Research
Since the findings of the EXPEDITION trial in 2003, research into cariporide has slowed. The increased risk of mortality associated with high concentrations and the lack of efficacy at low concentration make it unlikely that cariporide will reach market as a cardioprotective agent during ischaemia and reperfusion.
However, more recent research has been conducted into cariporide as an anti-cancer treatment. Through its inhibition of NHE1, cariporide may provide a mechanism for initiating internal acidification of cancer cells leading to apoptosis. Cancer cells utilize NHE1 in a unique mechanism of providing high intracellular pH and low extracellular pH, preventing internal acidification and leading to an efflux of H+ from tumor cells.
Patents
The first patent pertaining to cariporide use was submitted March 30, 1994 as an antiarrhythmic agent and was granted on January 8, 1997. Since then, multiple patents have been issued for the use, delivery, and investigation of cariporide. However, no drug has been approved and marketed with cariporide.