drugset / Trial / NCT04900337

Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC) Compared to Placebo and Best Available Care (BAT), for the Treatment of Moderate to Severe COVID-19 Patients.

NCT04900337 ↗

Phase 1/2 Completed 66 enrolled Amorphical Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase I/II study with Amorphous Calcium Carbonate (ACC) administered sublingual and in Inhalation concomitantly with BAT (Best Available Care) as Compared to Placebo and BAT for the treatment of Moderate to Severe COVID-19 patients. The purpose of this study is to assess the Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC).

Timeline

Start
2021-02-09
Primary completion
2023-06-30
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Amorphous Calcium Carbonate Unknown 1.14 % Inhaled
Subject Amorphous Calcium Carbonate Unknown 10 ml Inhaled
Subject Amorphous Calcium Carbonate Unknown 2000 mg Inhaled

Indications