Clinical Study


A phase II, multi-centre, randomized, parallel group, baseline-and withdrawal-controlled study in 36 patients with primary aldosteronism to determine the dose-dependent efficacy,safety and tolerability of DP13 after a 2-week single-blind placebo run-in period followed by a randomized 8-week double-blind treatment period. After an additional single-blind, 2-week DP13 placebo withdrawal period, patients are switched to standard of care.

Study Name: DP13 – A Phase II Study in Patients With Primary Aldosteronism

Status: Completed

Conditions: Primary aldosteronism

Interventions: Drug: DP-13

Locations: Ospedale Molinette, Torino, Italy, 10126

Study link:

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