drugset / Trial / NCT04252937

Adrecizumab Dose Escalation Safety and Tolerability Evaluation (ADESTE)

NCT04252937 ↗

Phase 2 Unknown 30 enrolled GREAT Network Italy
Non-randomizedSequentialOpen-labelTreatment

Summary

This is an open, standard therapy controlled clinical trial using a single intravenous infusion of HAM8101 (Adrecizumab) in patients hospitalized for AHF. This study will serve as a safety trial for HAM8101 (Adrecizumab) in AHF, using a dose escalating design. Acute Heart Failure (AHF), both as deterioration of chronic stable condition or "de novo" onset constitutes a major indication of particular interest and continues to be a major health problem, with millions of people being affected, still associated with high mortality and rehospitalization rates despite numerous attempts to improve the situation. It is believed that deteriorated vascular integrity and function, which manifests in various symptoms resulting from extravasation of fluid and solutes, is a key mechanism contributing to development and progression of the disease. Therefore, it is warranted to start a phase 2 safety and proof of concept study with a new investigational product (IMP) that enhances the plasma concentration of bio-ADM in the circulation to restore and stabilize the vascular integrity and function in patients with AHF after initial stabilization with the current standard of care (SoC).

Timeline

Start
2019-12-15
Primary completion
2021-12-31
Completion
2022-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ENIBARCIMAB Monoclonal antibody 0.5 mg/kg Intravenous
Subject ENIBARCIMAB Monoclonal antibody 2 mg/kg Intravenous
Subject ENIBARCIMAB Monoclonal antibody 8 mg/kg Intravenous

Indications