WHO ICTRP trial

A three months study evaluating if the potassium binder sodium zirconium…

EUCTR2018-000175-33-SK · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2018-000175-33-SK
Public title A three months study evaluating if the potassium binder sodium zirconium cyclosilicate can help manage a common side effect of heart failure treatment, and thereby allow heart failure treatment to be improved
Scientific title A Phase II, Randomised, Double-Blind, Placebo Controlled, Parallel-Group, Multicentre, Three Month Duration Potassium Reduction Initiative to Optimize RAAS Inhibition Therapy with Sodium Zirconium Cyclosilicate in Heart Failure (PRIORITIZE HF) - PRIORITIZE HF
Primary sponsor AstraZeneca AB
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Romania;United States;Hungary;Slovakia;Canada;Poland;Brazil;Russian Federation;Bulgaria
Conditions Heart Failure; Hyperkalaemia MedDRA version: 20.0 Level: LLT Classification code 10008908 Term: Chronic heart failure System Organ Class: 100000004849 ;Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
Interventions Trade Name: Lokelma Product Name: Sodium zirconium cyclosilicate OS Product Code: AZD7270 Pharmaceutical Form: Powder for oral suspension INN or Proposed INN: Sodium zirconium cyclosilicate CAS Number: 242800-27-7 Concentration unit: g…
Registration date Feb 8, 2019
Target size 280
Secondary IDs D9484C00001;NCT03532009;2018-000175-33-HU
Registry page clinicaltrialsregister.eu

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