STATCO19: Atorvastatin as Adjunctive Therapy in COVID-19

Sponsor
Mount Auburn Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04380402
Collaborator
(none)
300
1
2
22.4
13.4

Study Details

Study Description

Brief Summary

Objective: To assess whether adjunctive therapy of COVID-19 infection with atorvastatin reduces the deterioration in hospitalized patients and improves clinical outcome.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

COVID-19 is caused by SARS-CoV-2, a β-coronavirus that binds to the zinc peptidase angiotensin-converting enzyme 2 (ACE2). No drug is licensed to treat COVID-19, but adjunctive pharmacologic interventions have been proposed for their immunomodulatory effects, including statins. About 5% of cases are considered critical, with severe respiratory failure as well as myocarditis, and thromboses, and are associated with high fatality rate. Statins affect endothelial dysfunction and have anti-inflammatory and immunomodulatory effects.

This prospective, randomized, open-label trial of atorvastatin as adjunctive treatment of

COVID-19 in hospitalized patients aims to study:
  1. Will atorvastatin reduce progression to severe or critical COVID-19 disease and death compared to standard care?

  2. Will atorvastatin lead to improved clinical outcome of COVID-19 disease at 30 days compared to standard care?

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Open-label Trial of Atorvastatin as Adjunctive Treatment of COVID-19
Actual Study Start Date :
Jun 25, 2020
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
May 8, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment

40 mg

Drug: Atorvastatin
Atorvastatin 40 mg tablet
Other Names:
  • atorvastatin calcium
  • No Intervention: Control

    Standard care

    Outcome Measures

    Primary Outcome Measures

    1. Proportion of patients that progress to severe or critical requiring ICU admission and/or emergency salvage therapy, or death [30 days]

      Proportion of patients in each arm that progress to severe or critical requiring ICU admission and/or emergency salvage therapy, or death, as described by WHO Ordinal Scale for Clinical Improvement scores 5-8 with higher being worse.

    Secondary Outcome Measures

    1. Overall score of patients in each arm on Day 7 based on WHO Ordinal Scale for Clinical Improvement [7 days]

      Description of clinical status of patients in each arm based on WHO Ordinal Scale of Clinical Improvement on Day 7, scores 1-8 with higher being worse.

    2. Overall score of patients in each arm on Day 30 based on WHO Ordinal Scale for Clinical Improvement [30 days]

      Description of clinical status of patients in each arm based on WHO Ordinal Scale of Clinical Improvement on Day 30, scores 1-8 with higher being worse.

    3. Proportions of patients in each arm who test negative for SARS-CoV-2 on Day 7 [7 days]

      Proportions of patients in each arm who are tested on Day 7 and have negative PCR

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient aged 18-85 years, admitted with suspected COVID-19 disease based on clinical criteria (typical upper respiratory symptoms, e.g. runny nose, sore throat, dry cough, associated with COVID-19 infection).
    Exclusion Criteria:
    • already on chronic statin therapy, known hypersensitivity or adverse events to statins, negative nasopharyngeal (NP) swab for SARS-CoV-2, pregnancy and lactation, need for ICU admission, ALT or AST >2X upper limit of normal; CPK > 5x upper limit of normal; and creatinine clearance <50%, chronic treatment with colchicine, cyclosporin, digoxin, fusidic acid, azole antifungals, niacin.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mount Auburn Hospital Cambridge Massachusetts United States 02138

    Sponsors and Collaborators

    • Mount Auburn Hospital

    Investigators

    • Principal Investigator: Lin H Chen, MD, Mount Auburn Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Mount Auburn Hospital
    ClinicalTrials.gov Identifier:
    NCT04380402
    Other Study ID Numbers:
    • MountAuburn
    First Posted:
    May 8, 2020
    Last Update Posted:
    Mar 19, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 19, 2021