Official Title
Hydroxychloroquine in SARS-CoV-2 (COVID-19) Pneumonia Trial
Brief Summary

Novel coronavirus SARS(Severe Acute Respiratory Syndrome)-CoV-2 was first identified during the outbreak in Wuhan, China in December 2019 with the now resulting pandemic. Aggressive supportive care is the mainstay of treatment currently and rescue with lung protective mechanical ventilation is essential for survival in patients with severe acute respiratory distress syndrome. Despite supportive care, mortality is significant in hospitalized patients in the U.S., especially among patients > 65 years of age. Pharmacologic treatments to decrease disease severity are urgently needed. Hydroxychloroquine is currently widely used for treatment of autoimmune disease including systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and treat malaria. In vitro and in vivo antiviral activity towards SARS-CoV-2 has been reported. Since hydroxychloroquine has been used for decades its properties as a drug are well known. The investigators propose a pragmatic trial of hydroxychloroquine in moderately ill hospitalized adults with SARS-CoV-2 pneumonia with the hypothesis that hydroxychloroquine reduces severity of acute lung injury caused by SARS-CoV-2 infection.

Detailed Description

Novel coronavirus SARS-CoV-2 was first identified during the outbreak in Wuhan, China in
December 2019 with the now resulting pandemic. Aggressive supportive care is the mainstay of
treatment currently and rescue with lung protective mechanical ventilation is essential for
survival in patients with severe acute respiratory distress syndrome. Despite supportive
care, mortality is significant in hospitalized patients in the U.S., especially among
patients > 65 years of age. Pharmacologic treatments to decrease disease severity are
urgently needed. Candidate treatments with antiviral activity and/or immune-modulating
effects include hydroxychloroquine (HCQ), lopinavir/ritonavir, remdesivir, and tocilizumab
among others. There is limited high quality clinical data prompting a dilemma of how to use
and review potential treatments and ensure patient safety now as the pandemic begins to peak.
There are also significant limitations in drug supplies at many institutions.

Hydroxychloroquine is currently widely used for treatment of autoimmune disease including
systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and
treat malaria. In vitro and in vivo antiviral activity towards SARS-CoV-2 has been reported.
Since hydroxychloroquine has been used for decades its properties as a drug are well known.
Pertinent adverse events to monitor in a hospitalized patient include QTc (corrected QT
interval) prolongation, elevation of liver enzymes/acute liver injury, and hypokalemia.

Acute lung injury and progressive respiratory failure is the major cause of mortality in
SARS-CoV-2 infection. In acute lung injury and respiratory distress syndrome, the severity of
hypoxia is categorized by the Pao2/FIO2 (fraction of inspired oxygen) ration as mild (200 mm
Hg mm Hg). A persistently low Pao2/Fio2 ratio is associated with worse outcomes and may be a
marker of failure to respond to conventional therapy. PaO2/FIO2 is a clinically useful
measure in patients regardless of if they are receiving noninvasive supplemental O2 or
mechanical ventilation, and low ratios are associated with duration of ICU stay and hospital
mortality.

The care of hospitalized patients with covid-19 is evolving with hospital guidelines arising
across the U.S. with several commonalities. Patients receive clinical assessment, chest
x-ray, covid-19 testing, basic labs (WBC, CMP), and additional labs based on protocol or
clinical judgment (ABG, CRP-C reactive protein, LDH), antibiotics for possible bacterial
pneumonia, acetaminophen for fever, supplemental O2, close monitoring for worsening
respiratory status and consideration for mechanical ventilation. Since covid-19 is a novel
illness, there is no proven clinically efficacious drug treatment. Candidate drugs are being
used, some in the context of trials and others by physician discretion. Early intubation over
escalating noninvasive support (ie. High flow nasal canula and bipap) has been adopted due to
the frequency of rapidly worsening oxygenation, hemodynamic instability, and to protect staff
from virus aerosolization. Low tidal volume ventilation and prone positioning are lung
protective strategies used in critically ill covid-19 patients that are based on management
of acute respiratory distress syndrome generally. Arrhythmias, cardiomyopathy, and shock are
serious complications from covid-19 that warrant avoidance of acidosis, electrolyte
monitoring and replacement, and pressor support. Conservative fluid replacement is used to
avoid worsening oxygenation. In sum, multiple factors including timeliness and quality of
care likely affect patient outcomes. Hospitalists and pulmonary critical care physicians
direct the care of covid-19 patients with support from specialists as needed including
infectious disease, cardiology, and nephrology.

Pragmatic trials focus on studying the real-world effect of an intervention, such as a
medication, in the context of other care a patient is likely to receive. The intervention is
delivered by staff normally taking care of the patient with monitoring that is routinely
available. Advantages can include generalizability, increased physician participation due to
less burdensome study protocols, and feasibility. Disadvantages include allowance of
unblinded design, bias from physicians and patients about the intervention, and more
heterogeneity in treatment than in a mechanistic protocolized trial. Efforts to minimize bias
include selecting objective outcomes (e.g. PaO2/FIO2 rather than cough or dyspnea).

Withdrawn
SARS-CoV-2 Pneumonia
COVID-19

Drug: Hydroxychloroquine

Hydroxychloroquine is currently widely used for treatment of autoimmune disease including systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and treat malaria.
Other Name: Plaquenil

Eligibility Criteria

Inclusion Criteria:

1. Age > 18 years of age

2. SARS-CoV-2 positive per FDA approved RT-PCR (reverse transcription-polymerase chain
reaction)

3. Acute hypoxia (O2 sat < 90 % or paO2 < 60 on room air), or above baseline chronic O2
requirement

4. Inpatient admission

Exclusion Criteria:

1. Requires supplemental O2 >10 litres per minute or mechanical ventilation on admission

2. Pregnancy

3. AST/ALT > 5 times the upper limit normal

4. Baseline prolonged QT

5. Child-Pugh Score B or greater

6. ESRD(end-stage renal disease) requiring dialysis

7. Known allergy to medication component,

8. History of severe G6PD (glucose-6-phosphate dehydrogenase)

9. Myasthenia gravis

10. Porphyria

11. Ongoing treatment for epilepsy

12. Life expectancy < 6 months,

13. Patient lacks capacity to provide consent and does not have a surrogate decision
maker.

14. Retinal Disease

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

Kootenai Health
Coeur d'Alene, Idaho, United States

Washington State University
NCT Number
Keywords
SARS-CoV-2
Pneumonia
hydroxychloroquine
Covid-19
MeSH Terms
COVID-19
Pneumonia
Hydroxychloroquine