Company intelligence / Profile preview

Reprieve Cardiovascular

Milford, Massachusetts, United Stateslinkedin.com ↗

Ownership: Private
Development stage: Phase 2

Overview

The FASTR randomized pilot study demonstrated that the Reprieve System significantly improved sodium excretion, total urine output, and weight loss compared to optimal diuretic therapy in patients with ADHF. The system met both primary efficacy and safety endpoints without increasing adverse events. FDA approval has been granted for a pivotal IDE trial ("FASTR II") now launching in the US and Europe.

Therapeutic areas: Cardiovascular
Modalities: Device (specifically, an automated fluid management system for heart failure)Non-pharmacological therapy
Industry: Therapeutic Medical Devices

Drug pipeline

1 asset

Reprieve System

Phase 2

Indications: Acute decompensated heart failure

Partnerships

Over 150 healthcare provider partnerships across the United States to facilitate adoption of its therapies into standard care protocols

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