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PROTAGORAS: Protamine application in patients undergoing transfemoral TAVR

2024-512024-10-01Phase 3Authorised

Sponsor
LMU Klinikum
Start
Mar 2025
Modality
Recombinant Proteins and Enzymes
Countries
2
01

Overview

Phase 3 trial of protamine in aortic stenosis (AS), sponsored by LMU Klinikum. Primary endpoint: Primary: Bleeding grade ≥ type 2 (VARC) until 60 hours post TAVR procedure. Planned start Mar 2025; status: authorised.

02

Drugs

protamine
03

Conditions

aortic stenosis (AS)

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