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Pharmacopeia’s hypertension drug found effective in Phase I study

Biopharmaceutical company Pharmacopeia has reported additional positive results from the company's Phase I multiple-ascending dose study of its lead internal product candidate for hypertension.

PS433540 is a dual-acting angiotensin and endothelin receptor antagonist that is being developed as a potential treatment for hypertension and diabetic nephropathy. Data demonstrated that PS433540 produced statistically significant, dose-dependent increases in plasma-renin activity levels, as well as reductions in systolic and diastolic blood pressure.

These findings are in addition to previously reported initial results from the multiple-ascending dose trial that showed all doses of PS433540 to be safe and well-tolerated.

The trial’s positive plasma-renin activity and blood pressure findings provide preliminary insight into the potential of PS433540 to treat hypertension. Study investigators witnessed a dose-dependent increase in plasma-renin activity levels for PS433540, which was more pronounced at day 15 than at day one.

This observed increase in plasma-renin activity is indicative of PS433540’s ability to block the angiotensin receptor, a key target in efforts to lower and control blood pressure in hypertensive patients. Furthermore, associated with the increase in plasma-renin activity levels was a decrease in both diastolic and systolic blood pressure for PS433540 of up to 15mmHg.