Overview

LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF

Status:
RECRUITING
Trial end date:
2028-10-01
Target enrollment:
Participant gender:
Summary
This study will evaluate the efficacy of TNX-103 (oral levosimendan) compared with placebo in subjects with PH-HFpEF as measured by the change in 6-Minute Walk Distance (6 MWD; Day 1 to Week 12).
Phase:
PHASE3
Details
Lead Sponsor:
Tenax Therapeutics, Inc.
Collaborators:
Medpace, Inc.
Northwestern University