drugset / Trial / NCT05975021

A Safety and Efficacy Trial of Istaroxime for Cardiogenic Shock Stage C

NCT05975021 ↗

Phase 1/2 Active not recruiting 20 enrolled Windtree Therapeutics
RandomizedParallel-groupTriple-blindTreatment

Summary

The current trial aims to assess the effect of istaroxime in patients with SCAI Stage C Cardiogenic Shock (CS). These patients look unwell, frequently with a sudden change in mental status, mottled and cool extremities, and delayed capillary refill, as well as signs of congestion and relative low blood pressure and signs of hypoperfusion (reduced oxygen to organs) which frequently require support with rescue therapies including inotropes, vasopressors, or mechanical devices. Windtree Therapeutics, Inc. has been studying istaroxime, which has the potential to treat patients in this condition without some of the disadvantages of existing therapies being used to treat patients with acute heart failure and CS. Participants enrolled in this trial will receive standard of care (SoC) therapy for heart failure and CS. Additionally, half of the participants will be randomly chosen to receive istaroxime. Istaroxime has the potential to increase blood pressure and improve cardiac function.

Timeline

Start
2024-06-01
Primary completion
2025-07-28
Completion
2026-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Istaroxime Small molecule 0.5 ug/kg Intravenous

Indications