search
Back to results

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)

Primary Purpose

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Coronavirus Disease 2019 (COVID-19), Immunocompromised

Status
Withdrawn
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Nirmatrelvir
Ritonavir
Placebo for nirmatrelvir
Sponsored by
Pfizer
About
Eligibility
Locations
Arms
Outcomes
Full info

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

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Experimental

Arm Label

Nirmatrelvir/ritonavir

Placebo/ritonavir

Arm Description

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.

Outcomes

Primary Outcome Measures

Change from baseline in SARS-CoV-2 RNA level in nasopharyngeal (NP) swabs
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.

Secondary Outcome Measures

Time to sustained clinical recovery.
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir treatment on clinical outcomes when added to background usual care, for the treatment of severe COVID-19 in hospitalized participants. Time to sustained clinical recovery is defined as the first day during the 30 days after randomization in which a participant attains a score of 1, 2, or 3 on the 8-point ordinal scale (ie, remains alive and is either not hospitalized or is hospitalized but no longer requires ongoing inpatient medical care for COVID-19) for at least 7 consecutive days.
Proportion of participants with death from any cause or initiation of invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO)
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir treatment on clinical outcomes when added to background usual care, for the treatment of severe COVID-19 in hospitalized participants.
Proportion of participants with SARS-CoV-2 RNA <Lower Limit of Quantitation (<LLOQ) (defined as <2.0 log10 copies/mL) in NP swabs
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.
Proportion of participants with sustained NP swab SARS-CoV-2 RNA <LLOQ (defined as <2.0 log10 copies/mL)
To evaluate the effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.
Incidence of Treatment-Related Adverse Events (TEAEs)
To describe the safety and tolerability of nirmatrelvir/ritonavir relative to placebo/ritonavir for the treatment of severe COVID-19 in hospitalized participants.
Incidence of Adverse Events (AEs) or Serious Adverse Events (SAEs) leading to discontinuations
To describe the safety and tolerability of nirmatrelvir/ritonavir relative to placebo/ritonavir for the treatment of severe COVID-19 in hospitalized participants.

Full Information

First Posted
September 16, 2022
Last Updated
February 27, 2023
Sponsor
Pfizer
search

1. Study Identification

Unique Protocol Identification Number
NCT05545319
Brief Title
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
Acronym
EPIC-HOS
Official Title
AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2, DOUBLE-BLIND, 2-ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED NIRMATRELVIR/RITONAVIR COMPARED WITH PLACEBO/RITONAVIR FOR THE TREATMENT OF SEVERE COVID-19 IN HOSPITALIZED PARTICIPANTS WHO ARE IMMUNOCOMPROMISED OR AT INCREASED RISK FOR SEVERE COVID-19 OUTCOMES
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Termination due to challenges related to the operational feasibility of the study, taking into account the current epidemiology and declining hospitalization rates for severe COVID-19.
Study Start Date
December 13, 2022 (Anticipated)
Primary Completion Date
September 21, 2023 (Anticipated)
Study Completion Date
January 6, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pfizer

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Coronavirus Disease 2019 (COVID-19), Immunocompromised, Hospitalization, Child, Hospitalized
Keywords
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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nirmatrelvir/ritonavir
Arm Type
Experimental
Arm Description
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
Arm Title
Placebo/ritonavir
Arm Type
Experimental
Arm Description
Participants will receive placebo 0 mg/ritonavir 100 mg every 12 hours for 15 days.
Intervention Type
Drug
Intervention Name(s)
Nirmatrelvir
Other Intervention Name(s)
Paxlovid
Intervention Description
Participants will receive 2 tablets of nirmatrelvir (or 1 tablet for participants with eGFR or eCrCl ≥30 to <60 mL/min) every 12 hours
Intervention Type
Drug
Intervention Name(s)
Ritonavir
Other Intervention Name(s)
Norvir
Intervention Description
Participants will receive 1 capsule of ritonavir every 12 hours
Intervention Type
Drug
Intervention Name(s)
Placebo for nirmatrelvir
Intervention Description
Participants will receive 2 tablets of placebo for nirmatrelvir (or 1 tablet for participants with eGFR or eCrCl ≥30 to <60 mL/min) every 12 hours. A placebo does not have any medicine in it but looks just like the medicine being studied.
Primary Outcome Measure Information:
Title
Change from baseline in SARS-CoV-2 RNA level in nasopharyngeal (NP) swabs
Description
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.
Time Frame
Day 1 through Day 5
Secondary Outcome Measure Information:
Title
Time to sustained clinical recovery.
Description
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir treatment on clinical outcomes when added to background usual care, for the treatment of severe COVID-19 in hospitalized participants. Time to sustained clinical recovery is defined as the first day during the 30 days after randomization in which a participant attains a score of 1, 2, or 3 on the 8-point ordinal scale (ie, remains alive and is either not hospitalized or is hospitalized but no longer requires ongoing inpatient medical care for COVID-19) for at least 7 consecutive days.
Time Frame
Day 1 through Day 30
Title
Proportion of participants with death from any cause or initiation of invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO)
Description
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir treatment on clinical outcomes when added to background usual care, for the treatment of severe COVID-19 in hospitalized participants.
Time Frame
Day 1 through Day 30
Title
Proportion of participants with SARS-CoV-2 RNA <Lower Limit of Quantitation (<LLOQ) (defined as <2.0 log10 copies/mL) in NP swabs
Description
Evaluate effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.
Time Frame
Day 1 through Day 15
Title
Proportion of participants with sustained NP swab SARS-CoV-2 RNA <LLOQ (defined as <2.0 log10 copies/mL)
Description
To evaluate the effect of nirmatrelvir/ritonavir compared to placebo/ritonavir on SARS-CoV-2 viral RNA levels in NP swabs in hospitalized participants.
Time Frame
Day 15 through Day 45
Title
Incidence of Treatment-Related Adverse Events (TEAEs)
Description
To describe the safety and tolerability of nirmatrelvir/ritonavir relative to placebo/ritonavir for the treatment of severe COVID-19 in hospitalized participants.
Time Frame
Day 1 through Day 45
Title
Incidence of Adverse Events (AEs) or Serious Adverse Events (SAEs) leading to discontinuations
Description
To describe the safety and tolerability of nirmatrelvir/ritonavir relative to placebo/ritonavir for the treatment of severe COVID-19 in hospitalized participants.
Time Frame
Day 1 through Day 45

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pfizer CT.gov Call Center
Organizational Affiliation
Pfizer
Official's Role
Study Director
Facility Information:
Facility Name
Bassett Medical Center
City
Cooperstown
State/Province
New York
ZIP/Postal Code
13326
Country
United States
Facility Name
Harlem Hospital Center
City
New York
State/Province
New York
ZIP/Postal Code
10037
Country
United States
Facility Name
Multiprofile Hospital for Active Treatment - Sveti Nikolay Chudotvoretz
City
Lom
State/Province
Montana
ZIP/Postal Code
3600
Country
Bulgaria
Facility Name
Multiprofile Hospital for Active Treatment Sv. Ivan Rilski - Kozloduy EOOD
City
Kozloduy
State/Province
Vratsa
ZIP/Postal Code
3320
Country
Bulgaria
Facility Name
Multiprofile Hospital for Active Treatment - Haskovo AD
City
Haskovo
ZIP/Postal Code
6304
Country
Bulgaria
Facility Name
Specialized Hospital for Active Treatment of Pneumo-Phthisiatric Diseases - Haskovo EOOD
City
Haskovo
ZIP/Postal Code
6305
Country
Bulgaria
Facility Name
"Specialized Hospital for Active Treatment of Lung Diseases - Pernik" EOOD
City
Pernik
ZIP/Postal Code
2300
Country
Bulgaria
Facility Name
"University Multiprofile Hospital for Active Treatment - Dr. Georgi Stranski" EAD
City
Pleven
ZIP/Postal Code
5800
Country
Bulgaria
Facility Name
MHAT - Heart and Brain
City
Pleven
ZIP/Postal Code
5804
Country
Bulgaria
Facility Name
"Multiprofile Hospital for Active Treatment - Medical Complex Sveti Ivan Rilski" EOOD
City
Plovdiv
ZIP/Postal Code
4003
Country
Bulgaria
Facility Name
UMHAT "Prof. Dr. Stoyan Kirkovich"AD
City
Stara Zagora
ZIP/Postal Code
6003
Country
Bulgaria

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.
IPD Sharing URL
https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests
Links:
URL
https://pmiform.com/clinical-trial-info-request?StudyID=C4671031
Description
To obtain contact information for a study center near you, click here.

Learn more about this trial

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

We'll reach out to this number within 24 hrs