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Trial record 1 of 1 for:    EPIC-SR
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Evaluation of Protease Inhibition for COVID-19 in Standard-Risk Patients (EPIC-SR).

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT05011513
Recruitment Status : Recruiting
First Posted : August 18, 2021
Last Update Posted : April 13, 2022
Sponsor:
Information provided by (Responsible Party):
Pfizer

Study Description
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Brief Summary:
The primary hypothesis to be tested is whether or not there is a difference in time to sustained alleviation of all targeted COVID-19 signs and symptoms through Day 28 between PF-07321332/ritonavir and placebo.

Condition or disease Intervention/treatment Phase
COVID-19 Drug: PF-07321332 Drug: Ritonavir Drug: Placebo Phase 2 Phase 3

Detailed Description:
Throughout the study period, provision will be made to allow study visits to be conducted at a participant's home or at another non-clinic location, if available. The total study duration is up to 24 weeks.
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1980 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Eligible participants with a confirmed diagnosis of SARS-CoV-2 infection will be randomized (1:1) to receive PF-07321332/ritonavir or placebo orally every 12 hours for 5 days (10 doses total).
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description: Double-blind
Primary Purpose: Treatment
Official Title: AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2/3, DOUBLE-BLIND, 2 ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED PF 07321332/RITONAVIR COMPARED WITH PLACEBO IN NONHOSPITALIZED SYMPTOMATIC ADULT PARTICIPANTS WITH COVID-19 WHO ARE AT LOW RISK OF PROGRESSING TO SEVERE ILLNESS
Actual Study Start Date : August 25, 2021
Estimated Primary Completion Date : July 20, 2022
Estimated Study Completion Date : November 30, 2022

Resource links provided by the National Library of Medicine

Drug Information available for: Ritonavir

Arms and Interventions
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Arm Intervention/treatment
Experimental: PF-07321332/ritonavir
Orally administered PF-07321332+ritonavir
 Drug: PF-07321332
PF-07321332 (tablet)

Drug: Ritonavir
Ritonavir (capsule)
Placebo Comparator: Placebo
Orally administered Placebo
 Drug: Placebo
Placebo (tablet)

Drug: Placebo
Placebo (capsule)


Outcome Measures
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Primary Outcome Measures :
  1. Time to Sustained Alleviation of All Targeted COVID-19 Signs/Symptoms [ Time Frame: Baseline through Day 28 ]
    Analysis set includes COVID-19 symptom onset 1-3 days before treatment.


Secondary Outcome Measures :
  1. Percentage of Participants Who Experience Adverse Events (AEs) [ Time Frame: Baseline through Day 34 ]
  2. Percentage of Participants Who Experience an AE(s) or Serious Adverse Events (SAEs) that Leads to Study Discontinuation [ Time Frame: Baseline through Day 34 ]
  3. Proportion of Participants With Severe Signs/Symptoms Attributed to COVID-19 [ Time Frame: Baseline through Day 28 ]
  4. Time to Sustained Resolution of All Targeted COVID-19 Signs/Symptoms [ Time Frame: Baseline through Day 28 ]
  5. Duration of Each Targeted COVID-19 Sign/Symptom [ Time Frame: Baseline through Day 28 ]
  6. Proportion of Participants Progressing to a Worsening Status In 1 or More COVID-19 Signs/Symptoms [ Time Frame: Baseline through Day 28 ]
  7. Proportion of Participants With a Resting Peripheral Oxygen Saturation ≥95% [ Time Frame: Days 1, 5 ]
  8. Number of COVID-19 Related Medical Visits [ Time Frame: Baseline through Day 28 ]
  9. Number of Days in Hospital and Intensive Care Unit (ICU) Stay in Participants With COVID-19 Related Hospitalization [ Time Frame: Baseline through Day 28 ]
  10. Proportion of Participants With COVID-19 Related Hospitalization or Death From Any Cause [ Time Frame: Baseline through Day 28 ]
  11. Proportion of Participants With Death (all cause) [ Time Frame: Baseline through Week 24 ]
  12. Minimal Concentration (Ctrough) of PF-07321332 [ Time Frame: Baseline through Day 5 ]
  13. Viral Titers Measured Via Reverse Transcription Polymerase Chain Reaction (RT-PCR) in Nasal Swabs [ Time Frame: Baseline through Day 14 ]
  14. Time to Sustained Alleviation of All Targeted COVID-19 Signs/Symptoms [ Time Frame: Baseline through Day 28 ]
    Analysis set includes COVID-19 symptom onset 1-5 days before treatment.


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Confirmed SARS-CoV-2 infection 5 days prior to randomization
  • Initial onset of COVID-19 signs/symptoms within 5 days of randomization
  • Fertile participants must agree to use a highly effective method of contraception

Exclusion Criteria:

  • Has at least one underlying medical condition associated with an increased risk of developing severe illness from COVID-19
  • History of or need for hospitalization for the medical treatment of COVID-19
  • Prior diagnosis of SARS-CoV-2 infection (reinfection)
  • Known medical history of liver disease
  • Receiving dialysis or have known renal impairment
  • Known Human Immunodeficiency Virus (HIV) infection with viral load > 400 copies/ml or taking prohibited medications for HIV treatment
  • Suspected or confirmed concurrent active systemic infection other than COVID-19
  • Current or expected use of any medications or substances that are highly dependent on Cytochrome P450 3A4 (CYP3A4) for clearance or are strong inducers of CYP3A4
  • Has received or is expected to receive monoclonal antibody treatment or convalescent COVID-19 plasma
  • Has received any SARS-CoV-2 vaccine within 12 months of screening
  • Participating in another interventional clinical study with an investigational compound or device, including those for COVID-19
  • Known prior participation in this trial or other trial involving PF-07321332
  • Oxygen saturation of < 92% on room air
  • Females who are pregnant or breastfeeding
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05011513


Contacts
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Contact: Pfizer CT.gov Call Center 1-800-718-1021 ClinicalTrials.gov_Inquiries@pfizer.com

Locations
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Sponsors and Collaborators
Pfizer
Investigators
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Study Director: Pfizer CT.gov Call Center Pfizer
More Information
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Additional Information:

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Responsible Party: Pfizer
ClinicalTrials.gov Identifier: NCT05011513    
Other Study ID Numbers: C4671002
2021-002857-28 ( EudraCT Number )
EPIC-SR ( Other Identifier: Alias Study Number )
First Posted: August 18, 2021    Key Record Dates
Last Update Posted: April 13, 2022
Last Verified: April 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
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.
URL: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Pfizer:
SARS-CoV-2 Infection
Additional relevant MeSH terms:
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COVID-19
Respiratory Tract Infections
Infections
Pneumonia, Viral
Pneumonia
Virus Diseases
Coronavirus Infections
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Lung Diseases
Respiratory Tract Diseases
 Ritonavir
HIV Protease Inhibitors
Viral Protease Inhibitors
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Anti-HIV Agents
Anti-Retroviral Agents
Antiviral Agents
Anti-Infective Agents
Cytochrome P-450 CYP3A Inhibitors
Cytochrome P-450 Enzyme Inhibitors