CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


0.9% sodium chloride (normal saline)Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug790 Stannous protoporphyrin (90mg) Wiki 1.00

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D018450 Disease Progression NIH 0.38

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Phase 2, Randomized, Placebo-Controlled Study to Evaluate the Effect of RBT-9 on Preventing Progression of COVID-19 in High-Risk Individuals

The overall objective is to evaluate the efficacy, tolerability, and safety of a single dose of RBT-9 (Stannous protoporphyrin) versus placebo in preventing the progression of coronavirus disease 2019 (COVID-19) infection in non-critically ill adults who are at high risk due to age or comorbid conditions.

NCT04364763 COVID19 Drug: Stannous protoporphyrin (90mg) Drug: 0.9% sodium chloride (normal saline)
MeSH:Disease Progression

Primary Outcomes

Description: Determining severity of COVID-19 in patients measured using the 8-point World Health Organization (WHO) Ordinal Clinical Scale measures the clinical status of a subject at the first assessment of a given day with category 1 most favorable and category 8 least favorable(1. Ambulatory, no limitation of activities; 2. Ambulatory, limitation of activities; 3. Hospitalized, no oxygen therapy; 4. Hospitalized, oxygen by mask or nasal prongs; 5. Hospitalized, non-invasive ventilation or high-flow oxygen; 6. Hospitalized, intubation and mechanical ventilation; 7. Hospitalized, ventilation plus additional organ support - pressors, renal replacement therapy [RRT], extracorporeal membrane oxygenation [ECMO]; 8. Death)

Measure: Evaluate the effect of RBT-9(stannous protoporphyrin) versus placebo on clinical status of Covid-19 patients as measured using the 8-point World Health Organization (WHO) Ordinal Clinical Scale

Time: 28 days

Secondary Outcomes

Description: Time to first occurrence of either death from any cause or new/worsened organ dysfunction through Day 28, defined as at least one of the following: 1. Respiratory decompensation; 2. New or worsening congestive heart failure; 3. Requirement of vasopressor therapy and/or inotropic or mechanical circulatory support; 4. Ventricular tachycardia or fibrillation lasting at least 30 seconds and/or associated with hemodynamic instability or pulseless electrical activity, or resuscitated cardiac arrest; 5. Initiation of renal replacement therapy

Measure: Time to first occurrence of death from any cause or new/worsened organ dysfunction

Time: 28 Days

Description: Percentage of subjects who are alive at Day 28

Measure: All-cause survival

Time: 28 Days

Description: Among subjects who begin oxygen therapy, mean change from initiation to last day on oxygen or Day 28 (whichever happens first) in respiratory distress rate

Measure: Respiratory distress rate

Time: 28 Days

Description: Percentage of subjects with fever through Day 28

Measure: Fever incidence

Time: 28 Days

Description: Percentage of subjects who develop AKI (defined as an increase in serum creatinine by 0.5 mg/dL or more within 48 hours or an increase in serum creatinine to 1.5 × Baseline or more within the last 7 days) through Day 28

Measure: Acute kidney injury (AKI) incidence

Time: 28 Days

Description: Percentage of subjects with new or worsening congestive HF at Day 28

Measure: New or worsening congestive heart failure (HF)

Time: 28 Days

Description: Percentage of subjects who remain hospitalized at Day 28

Measure: Hospitalization status

Time: 28 Days

Description: Percentage of subjects with ventricular tachycardia or fibrillation lasting at least 30 seconds and/or associated with hemodynamic instability or pulseless electrical activity, or resuscitated cardiac arrest at Day 28

Measure: Ventricular tachycardia or fibrillation lasting at least 30 seconds and/or associated with hemodynamic instability or pulseless electrical activity, or resuscitated cardiac arrest

Time: 28 Days

Description: Number of oxygen-free days through Day 28

Measure: Oxygen-free days

Time: 28 Days

Description: Percentage of subjects transferred to the ICU through Day 28

Measure: Intensive care unit (ICU) status

Time: 28 Days

Description: Number of days on mechanical ventilation through Day 28

Measure: Days on ventilator

Time: 28 Days

Description: Time to and duration of vasopressor or inotrope utilization through Day 28

Measure: Time to and duration of vasopressor or inotrope utilization

Time: 28 Days

Description: Percentage of subjects who begin dialysis through Day 28

Measure: Dialysis status

Time: 28 Days


No related HPO nodes (Using clinical trials)