Ulinastatin for the Treatment of COVID-19 in Hospitalized Patients

Trial ID or NCT#

NCT04393311

Status

not recruiting iconNOT RECRUITING

Purpose

The primary objective of this study is to evaluate the safety and efficacy of intravenous (IV) infusion of ulinastatin compared to placebo with respect to time to recovery, disease severity, need for ventilator support, and mortality in patients with COVID 19.

Official Title

A Multi-Center, Randomized, Double-Blind, Placebo Controlled Study of the Safety and Efficacy of Ulinastatin for the Treatment of COVID-19 in Hospitalized Patients

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - Willing and able to provide written informed consent - Signs and symptoms suggestive of COVID-19 infection - Laboratory-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection ≤7 days before randomization - Currently hospitalized or in an emergency department with planned hospitalization - Peripheral capillary oxygen saturation (SpO2) <93% on room air at Screening
Exclusion Criteria:
  1. - Simultaneous participation in any other clinical study incompatible with this one - Treatment with an antibody immunotherapy within 4 weeks of Screening - Requirement for mechanical ventilation or ECMO at Screening - Hypotension at Screening - Severe liver injury defined as AST or ALT ≥5x the upper limit of normal - Severe kidney failure defined as an estimated glomerular filtration rate (eGFR) <30 mL/min - Pregnancy or breastfeeding - > 120 hours between admission and signing consent
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Investigator(s)

Kevin Grimes
Kevin Grimes
Professor (Teaching) of Chemical and Systems Biology

View on ClinicalTrials.gov