Title

A Pilot Study to Assess Safety and Efficacy of SIR1-365 in Patients With Severe COVID-19
A Multicenter, Randomized, Double-Blinded, Placebo-Controlled Study to Assess Safety and Efficacy of SIR1-365 in Patients With Severe COVID-19
  • Phase

    Phase 1
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    SIR1-365 ...
  • Study Participants

    45
Primary Objective:

• To evaluate overall safety and tolerability of SIR1-365 in patients with severe COVID-19

Secondary Objectives:

To assess the clinical efficacy of SIR1-365 in patients with severe COVID-19
To assess the effects of SIR1-365 on multiple inflammatory biomarker levels including C-reactive protein (CRP), ferritin, lymphocyte and neutrophil counts, cytokines, and chemokines
To assess the effects of SIR1-365 on biomarkers indicative of target engagement in patients with severe COVID-19
To assess the effects of SIR1-365 on biomarkers indicative of kidney injury in patients with severe COVID-19
To assess the effects of SIR1-365 on biomarkers indicative of cardiovascular endothelial cell damage in patients with severe COVID-19
To characterize plasma pharmacokinetics (PK) of SIR1-365 in patients with severe COVID-19
Study duration per participant is approximately 28 days including a 14-day treatment period
Study Started
Dec 18
2020
Primary Completion
Nov 27
2021
Study Completion
Nov 27
2021
Last Update
Mar 24
2022

Drug SIR1-365

Route of administration: oral

  • Other names: Pharmaceutical form: tablets

Drug Matching Placebo

Route of administration: oral

  • Other names: Pharmaceutical form: tablets

SIR1-365 Experimental

SIR1-365 dose 1 daily for 14 days

Matching placebo Placebo Comparator

Matching placebo dose 1 daily for 14 days

Criteria

Inclusion Criteria:

Hospitalized patient with clinical diagnosis of SARS-CoV-2 virus infection per World Health Organization criteria including positive nucleic acid test of any specimen (e.g., respiratory, blood, or other bodily fluid) within 2 weeks prior to screening.
Symptoms suggestive of severe systemic illness with COVID-19, which could include any of the following symptoms: fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, or shortness of breath at rest, or respiratory distress.
Clinical signs indicative of severe systemic illness with COVID-19, which could include any of the following clinical signs: respiratory rate ≥ 30 per minutes, heart rate ≥ 125 per minute, SpO2 ≤ 93% on room air, or PaO2/FiO2 ratio < 300 mmHg.
Men or women ≥18 but ≤80 years of age at the time of signing the informed consent.
Patient is able to understand the purpose and risks of the study and provide signed and dated informed consent or have a legal representative provide consent and authorization to use protected health information (in accordance with national and local patient privacy regulations).

Exclusion Criteria:

Patient requires endotracheal intubation and mechanical ventilation, oxygen delivered by high-flow nasal cannula (heated, humidified, oxygen delivered via reinforced nasal cannula at flow rates >20 L/min with fraction of delivered oxygen ≥ 0.5), noninvasive positive pressure ventilation, extracorporeal membrane oxygenation (ECMO), or clinical diagnosis of respiratory failure.
Patient with shock defined by systolic blood pressure < 90 mm Hg, or diastolic blood pressure < 60 mm Hg or requiring vasopressor.
Patient with multi-organ dysfunction or failure defined by an increase in the Sequential Organ Failure Assessment score of 2 points or more.
Patient is unlikely to survive beyond 2 days at the discretion of Investigator.
Patient has used chronic systemic corticosteroids within 2 weeks prior to screening.
Patient with positive results for human immunodeficiency virus (HIV) or hepatitis B or C test.
Patient has known active tuberculosis (TB), history of uncontrolled TB, suspected or known systemic bacterial or fungal infections within 4 weeks prior to screening.
Patient has any other condition, which makes the patient unsuitable for study participation
No Results Posted