The effective medical treatment against COVID-19 infection is still unknown. Chloroquine phosphate is a well-known antimalarial drug which has been on the market for many years. Recently, in vitro study shown that Chloroquine is effective at both entry and at post-entry stages of the COVID-19 infection of Vero E6 cells with promising results. Chloroquine is also an immune-modifier and could distribute to the whole body including lung. Also, chloroquine is cheap and safe, and could be a promising agent against COVID-19 infection. However, only hydroxychloroquine (HCQ) with the extra hydroxyl group is available in Taiwan. Therefore, hydroxychloroquine instead become the best choice for the treatment candidate, since it shows higher in vitro potency (EC50) against COVID-19 with lower toxicity while retaining the original effect which compared with chloroquine.
On December 31, 2019, an outbreak of respiratory illness later proved to be caused by a novel
coronavirus, officially named Coronavirus Disease 2019 (COVID-19), was notified first in
Wuhan, a city of Hubei province, People's Republic of China (PRC). COVID-19 rapidly spreads
in China and to other parts of the world. Currently more than 370,000 laboratory-confirmed
cases have been reported worldwide, and the case count has been rising daily, and caused a
global health emergency. As of March 29, 2020, there were 298 confirmed cases in Taiwan.
This is a multi-center, randomized, open-label, controlled trial to evaluate the efficacy and
tolerability of Hydroxychloroquine Sulfate (HCQ) in adult Patients with mild to moderate
coronavirus disease (COVID-19) compared to standard of care treatment (SOC). The primary
endpoint for the study is to evaluate the efficacy of HCQ, with respect to the time to
negatively rRT-PCR assessments from the randomization date up to 14 days. The secondary
endpoint is to evaluate the efficacy of HCQ in the aspect of virological assessments and the
change of clinical symptoms. In addition, the safety and tolerability of HCQ will be
evaluated during treatment period in COVID-19 patients.
Drug: Hydroxychloroquine Sulfate 200 MG [Plaquenil]
Hydroxychloroquine Sulfate is 400 mg bid on Day 1 and 200 mg bid for 6 days on Day 2-7.
Other Name: Plaquenil
Inclusion Criteria:
1. Patients who had fever (central temperature ≥38°C) or acute upper respiratory symptoms
and laboratory confirmation (rRT-PCR) for COVID-19, with available same type of upper
respiratory tract specimens from screening evaluation to the initial testing within 4
days of initial testing
2. Patients have mild (no pneumonia) to moderate disease (pneumonia without respiratory
distress) according to the following World Health Organization (WHO) definition of
COVID-19 clinical syndromes:
- Mild (Mild illness):
Patients with uncomplicated upper respiratory tract viral infection, may have
non-specific symptoms such as fever, fatigue, cough (with or without sputum
production), anorexia, malaise, muscle pain, sore throat, dyspnea, nasal congestion,
or headache. Rarely, patients may also present with diarrhoea, nausea and vomiting.
- Moderate (Pneumonia):
Adult with pneumonia but no signs of severe pneumonia and no need for supplemental
oxygen.
3. Willing and able to comply with the study procedure and sign a written informed
consent
Exclusion Criteria:
1. Patients with the medical history of hypersensitivity to chloroquine, chloroquinine,
or hydroxychloroquine
2. Patients with retinal disease, hearing loss, severe neurological and mental illness
3. Patients with pancreatitis
4. Patients with severe lung, liver (alanine aminotransferase (ALT)/aspartate
aminotransferase (AST) elevation more than 3 times the normal upper limit), kidney
(estimated glomerular filtration rate [eGFR] <30 mL/min/1.73m2, using the MDRD or
CKD-EPI methods), brain, haematological diseases or other important systemic diseases
5. Medical history of uncontrolled but clinically significant abnormal cardiac conduction
abnormalities at electrocardiogram (ECG) at screening, any history or evidence of long
QT syndrome or QTcF interval >450 msec for males and >470 msec for females (according
to Fridericia's correction) at screening
6. Known HIV infection; active hepatitis B or C without concurrent treatment (positive
tests for hepatitis B [both HBsAg and HBeAg], or high titer of hepatitis C ribonucleic
acid [RNA] >800,000 IU/ml)
7. Uncontrolled and unstable concurrent medical condition including psychiatric disorders
and alcohol/substance dependence/abuse that will jeopardize the safety of the patient,
interfere with the objectives of the study, or affect the patient compliance with
study requirements, as determined by the Investigator
8. Patients with concomitant use of medications that alter the absorption or excretion of
hydroxychloroquine
9. Patients were considered to be unable to complete the study, or not suitable for the
study judged by Investigators
10. Pregnant or breast-feeding women
Taoyuan General Hospital, Ministry of Health and Welfare
Taoyuan City, Taiwan
Shu-Hsing Cheng, Dr., Principal Investigator
Taoyuan General Hospital, Ministry of Health and Welfare