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Ensayos Clínicos

An observer-blind, multi-center, placebo-controlled, parallel group study to assess the safety and tolerability and to characterize the pharmacokinetics and the pharmacodynamics of different doses of BAY 1213790 in patients with end-stage renal disease undergoing hemodialysis

Ficha Técnica

Investigador Principal

ALEJANDRO MARTÍN MALO

Promotor

BAYER AG

ESTADO

ACTIVO

DEPARTAMENTO

Nefrología

Código EudraCT: 2018-003109-24

Número protocolo: BAY1213790/20046

Fecha Inicio: 2018-12-04

Fecha Fin: 2020-02-01