Double Therapy With IFN-beta 1b and Hydroxychloroquine

Sponsor

The University of Hong Kong (Other)

Overall Status

Completed

CT.gov ID

NCT04350281

Collaborator

(none)

Enrollment

Location

Arms

2.9

Actual Duration (Months)

20.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The novel coronavirus (SARS-CoV-2), is a single-stranded RNA coronavirus. The virus was first isolated from patients presented with pneumonia in Wuhan in December 2019. Sequences of the Wuhan betacoronavirus show similarities to betacoronaviruses found in bats, sharing a common ancestor with the 2003 SARS coronavirus (SARS-CoV) and the bat coronavirus HKU9, a virus found in fruit bats. Similar to SARS-CoV, it is a member of Beta-CoV lineage B. Five genomes of the novel coronavirus have been initially isolated and reported including BetaCoV/Wuhan/IVDC-HB-01/2019, BetaCoV/Wuhan/IVDC-HB-04/2020, BetaCoV/Wuhan/IVDC-HB-05/2019, BetaCoV/Wuhan/WIV04/2019, and BetaCoV/Wuhan/IPBCAMS-WH-01/2019 from the China CDC.

The SARS-CoV-2 has since spread from China to the rest of the world. As of 5 April 2020, more than 1.05 million people been confirmed to have infected by SARS-CoV-2, resulting in more than 500,000 deaths. No specific antiviral treatment for the SARS-CoV-2 is currently available, but existing medication could be repurposed.

Genetic sequencing demonstrated similarity of the SARS-CoV-2 to the SARS-CoV and MERS CoV.2 We expect patients infected with the SARS-CoV-2 will also present similarly with initial upper respiratory tract symptoms including fever, cough, sputum, myalgia and shortness or breath. More severe cases might complicate with pneumonia and required ventilatory or ECMO support. According to our previous studies in 2003 on patients hospitalized for severe SARS-CoV, the viral load peaked between day 7 from symptoms onset and coincided with clinical deterioration of pneumonia and respiratory failure, with majority of the patients required intensive care support. Higher viral load isolated from different human system also correlated with worsened SARS manifestation and complications.

Previously, the investigators have demonstrated that interferon-beta 1b, commonly used in the treatment of multiple sclerosis and lopinavir/ ritonavir, also demonstrated to improve the outcome of MERS-CoV infection in a non-human primate model of common marmoset.

A non-randomized trial has also suggested that a combination of hydroxychloroquine and azithromycin might be effective in suppressing SARS-CoV-2 viral load in patients, despite in-vitro activity was only found in hydroxychloroquine.

Therefore, the investigators propose to conduct an open-label randomized controlled trial on a short course of interferon β-1b and hydroxychloroquine combination treatment for patients hospitalized for COVID-19 infection.

Condition or Disease	Intervention/Treatment	Phase
COVID	Drug: Interferon Beta-1B Drug: Hydroxychloroquine	Phase 2

Detailed Description

This is a prospective open-label randomised controlled trial among adult patients hospitalised after April 2020 for virologically confirmed SARS-CoV-2 infection.

Patients will be randomly assigned to either the treatment group: a 3-day course of 3 doses of subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) consecutively on day 1 to day 3 and hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days plus standard care, or the control group: a 3-day course of hydroxycholoroquine 800mg on day 1, then 400mg daily for 2 days plus standard care alone (1:1).

For the control group, if the day 4 nasopharyngeal swab (NPS) viral load remains positive, then patients will receive another 3 days of subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) and hydroxychloroquine 400mg daily.

Study Design

Study Type:

Interventional

Actual Enrollment :

60 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-label Randomized Controlled Trial on Interferon β-1b and Hydroxychloroquine Combination Versus Hydroxychloroquine Alone, as Treatment for COVID-19 Infection

Actual Study Start Date :

Apr 9, 2020

Actual Primary Completion Date :

Jul 1, 2020

Actual Study Completion Date :

Jul 7, 2020

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Treatment group Subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) consecutively on day 1 to day 3 and hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days plus standard care	Drug: Interferon Beta-1B Daily subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) consecutively on day 1 to day 3 Drug: Hydroxychloroquine Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days
Active Comparator: Control group Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days plus standard care alone.	Drug: Hydroxychloroquine Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days

Arm

Intervention/Treatment

Active Comparator: Treatment group

Subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) consecutively on day 1 to day 3 and hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days plus standard care

Drug: Interferon Beta-1B

Daily subcutaneous injection of interferon β-1b 1mL (0.25mg; 8 million IU) consecutively on day 1 to day 3

Drug: Hydroxychloroquine

Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days

Active Comparator: Control group

Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days plus standard care alone.

Drug: Hydroxychloroquine

Hydroxychloroquine 800mg on day 1, then 400mg daily for 2 days

Outcome Measures

Primary Outcome Measures

Time to negative NPS viral load [4 weeks]
Time to negative NPS SARS-CoV-2 viral RT-PCR

Secondary Outcome Measures

Time to NEWS 0 [4 weeks]
Time to complete allevation of symptoms as defined by NEWS of 0 maintained for 24 hours
Length of Hospitalisation [4 weeks]
Days of hospital stay
Time to negative viral load in all clinical samples [4 weeks]
Time to negative SARS-CoV-2 viral RT-PCR in all clinical samples
Adverse events [4 weeks]
Treatment related adverse events
Mortality [30 days]
30-day mortality
Inflammatory markers changes [4 weeks from diagnosis]
Cytokine/ chemokine

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Recruited subjects include all adult patients ≥18 years hospitalized for virologic confirmed SARS-CoV-2 infection.
All subjects give written informed consent. For patients who are critically ill, requiring ICU, ventilation or confused, informed consent will be obtained from spouse, next-of-kin or legal guardians.
Subjects must be available to complete the study and comply with study procedures. Willingness to allow for serum samples to be stored beyond the study period, for potential additional future testing to better characterize immune response.

Exclusion Criteria:

Inability to comprehend and to follow all required study procedures.
Allergy or severe reactions to the study drugs
Patients with known prolonged QTc syndrome, ventricular cardiac arrhythmias, including torsade de pointes, second or third degree heart block, QTc interval >480ms
Patients taking medication that will potentially interact with l interferon beta-1b or hydroxychloroquine
Patients with known underlying retinopathy
Patients with G6PD deficiency
Patients with known history of severe depression
Received an experimental agent (vaccine, drug, biologic, device, blood product, or medication) within 1 month prior to recruitment in this study or expect to receive an experimental agent during this study.
To participate in an unrelated trial during the current clinical trial. Nevertheless, the patients have the right to withdraw from the current clinical trial to join another clinical trial.
Have a history of alcohol or drug abuse in the last 5 years.
Have any condition that the investigator believes may interfere with successful completion of the study.