A Study to Learn About the Medicine Called Nirmatrelvir Used in Combination With Ritonavir in People With Weakened Immune Systems or at Increased Risk for Poor Outcomes Who Are Hospitalized Due to Severe COVID-19 (EPIC-HOS)
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Coronavirus Disease 2019 (COVID-19), Immunocompromised
About this trial
This is an interventional treatment trial for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) focused on measuring COVID-19, Respiratory Tract Infections, Infections, Pneumonia, Viral, Pneumonia, Virus Diseases, Coronavirus Infections, Coronaviridae Infections, Nidovirales Infections, Ribonucleic acid (RNA) virus Infections, Lung Diseases, Respiratory Tract Diseases, Ritonavir, HIV Protease Inhibitors, Viral Protease Inhibitors, Protease Inhibitors, Enzyme Inhibitors, Molecular Mechanisms, Pharmacological Action, Anti-human immunodeficiency virus (HIV) Agents, Anti-Retroviral Agents, Antiviral Agents, Anti-Infective Agents, Cytochrome P-450 CYP3A Inhibitors, Cytochrome P-450 Enzyme Inhibitors, Paxlovid, Nirmatrelvir
Eligibility Criteria
Inclusion Criteria:
- Meeting 1 of the 2 categories of COVID-19 risk:
- Category A: Immunocompromised
- Category B: Non-Immunocompromised, but with ≥2 risk factors
- Onset of signs/symptoms attributable to COVID-19 ≤10 days prior to the day of randomization for non-immunocompromised participants (Category B).
- Confirmed SARS-CoV-2 infection as determined by Reverse transcription polymerase chain reaction (RT-PCR) or acceptable test method performed by a health care provider in any specimen collected within 48 hours prior to randomization.
- Hospitalized for inpatient care for the treatment of clinical manifestations of severe COVID-19.
- Requirement for oxygen supplementation (via nasal cannula, mask, non-invasive ventilation [NIV] or high flow oxygen) to maintain SpO2 ≥94% at the time of Screening and Randomization.
Exclusion Criteria:
- Critical illness, defined by ≥1 of the following:
- Requirement for mechanical ventilation or extracorporeal membrane oxygenation (ECMO) at randomization, or likely to require intermittent mandatory ventilation (IMV) or ECMO within 12 hours of randomization .
- Multi-organ dysfunction/failure.
- Hemodynamically unstable, eg. septic shock, cardiac failure or requiring vasopressors.
- Participant not expected to survive 24 hours from time of randomization.
- History of severe chronic liver disease
- Receiving dialysis of any kind or severe renal impairment
- Use of nirmatrelvir/ritonavir as an outpatient to treat the current COVID-19 related illness ≤7 days of randomization
Sites / Locations
- Bassett Medical Center
- Harlem Hospital Center
- Multiprofile Hospital for Active Treatment - Sveti Nikolay Chudotvoretz
- Multiprofile Hospital for Active Treatment Sv. Ivan Rilski - Kozloduy EOOD
- Multiprofile Hospital for Active Treatment - Haskovo AD
- Specialized Hospital for Active Treatment of Pneumo-Phthisiatric Diseases - Haskovo EOOD
- "Specialized Hospital for Active Treatment of Lung Diseases - Pernik" EOOD
- "University Multiprofile Hospital for Active Treatment - Dr. Georgi Stranski" EAD
- MHAT - Heart and Brain
- "Multiprofile Hospital for Active Treatment - Medical Complex Sveti Ivan Rilski" EOOD
- UMHAT "Prof. Dr. Stoyan Kirkovich"AD
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Nirmatrelvir/ritonavir
Placebo/ritonavir
Participants will receive nirmatrelvir/ ritonavir 300 mg/100 mg (or 150 mg/100 mg for participants with estimated glomerular filtration rate (eGFR) or estimated creatinine clearance (eCrCl) ≥30 to <60 mL/min) every 12 hours from Day 1 through Day 15
Participants will receive placebo 0 mg/ritonavir 100 mg every 12 hours for 15 days.