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.
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Amorphous Calcium Carbonate | Unknown | 1.14 % | Inhaled |
| Subject | Amorphous Calcium Carbonate | Unknown | 10 ml | Inhaled |
| Subject | Amorphous Calcium Carbonate | Unknown | 2000 mg | Inhaled |