Safety and efficacy of four drug regimens versus standard-of-care for the treatment of symptomatic outpatients with COVID-19: A randomised, open-label, multi-arm, phase 2 clinical trialResearch in context
Nomathemba Chandiwana,
Chelsea Kruger,
Hilary Johnstone,
Mohamed Farouk Chughlay,
Chung Ju,
Byungsu Kim,
Yengiwe Dineka,
Sarah Arbe-Barnes,
Robert Miller,
Andrew Owen,
Andrew Hill,
Daniel Windgassen,
Nada Abla,
Anne Claire Marrast,
Stephan Duparc,
Willem Daniel Francois Venter
Affiliations
Nomathemba Chandiwana
Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa; Corresponding author. Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Building C, Sunnyside Office Park, 32 Princess of Wales Terrace, Parktown, Johannesburg, South Africa.
Chelsea Kruger
Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Hilary Johnstone
HJ-Clinical Trial Consultancy, George, South Africa
Mohamed Farouk Chughlay
Medicines for Malaria Venture, Geneva, Switzerland
Chung Ju
Shin Poong Pharm. Co. Ltd., Seoul, Republic of Korea; Graduate School of Clinical Pharmacy, CHA University, Pocheon-si, Gyeonggi-do, Republic of Korea
Byungsu Kim
Shin Poong Pharm. Co. Ltd., Seoul, Republic of Korea
Yengiwe Dineka
Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Sarah Arbe-Barnes
Artemida Pharma, Stevenage, United Kingdom
Robert Miller
Artemida Pharma, Stevenage, United Kingdom
Andrew Owen
Department of Molecular and Clinical Pharmacology, Centre of Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, United Kingdom
Andrew Hill
Department of Molecular and Clinical Pharmacology, Centre of Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, United Kingdom
Daniel Windgassen
DATAMAP, Freiburg, Germany
Nada Abla
Medicines for Malaria Venture, Geneva, Switzerland
Anne Claire Marrast
Medicines for Malaria Venture, Geneva, Switzerland
Stephan Duparc
Medicines for Malaria Venture, Geneva, Switzerland
Willem Daniel Francois Venter
Ezintsha, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Summary: Background: This exploratory study investigated four repurposed anti-infective drug regimens in outpatients with COVID-19. Methods: This phase 2, single centre, randomised, open-label, clinical trial was conducted in South Africa between 3rd September 2020 and 23rd August 2021. Symptomatic outpatients aged 18–65 years, with RT-PCR confirmed SARS-CoV-2 infection were computer randomised (1:1:1:1:1) to standard-of-care (SOC) with paracetamol, or SOC plus artesunate-amodiaquine (ASAQ), pyronaridine-artesunate (PA), favipiravir plus nitazoxanide (FPV + NTZ), or sofosbuvir-daclatasvir (SOF-DCV). The primary endpoint was the incidence of viral clearance, i.e., the proportion of patients with a negative SARS-CoV-2 RT-PCR on day 7, compared to SOC using a log-binomial model in the modified intention-to-treat (mITT) population. Findings: The mITT population included 186 patients: mean age (SD) 34.9 (10.3) years, body weight 78.2 (17.1) kg. Day 7 SARS-CoV-2 clearance rates (n/N; risk ratio [95% CI]) were: SOC 34.2% (13/38), ASAQ 38.5% (15/39; 0.80 [0.44, 1.47]), PA 30.3% (10/33; 0.69 [0.37, 1.29]), FPV + NTZ 27.0% (10/37; 0.60 [0.31, 1.18]) and SOF-DCV 23.5% (8/34; 0.47 [0.22, 1.00]). Three lower respiratory tract infections occurred (PA 6.1% [2/33]; SOF-DCV 2.9% [1/34]); two required hospitalisation (PA, SOF-DCV). There were no deaths. Adverse events occurred in 55.3% (105/190) of patients, including one serious adverse event (pancytopenia; FPV + NTZ). Interpretation: There was no statistical difference in viral clearance for any regimen compared to SOC. All treatments were well tolerated. Funding: Medicines for Malaria Venture, with funding from the UK Foreign, Commonwealth and Development Office, within the Covid-19 Therapeutics Accelerator in partnership with Wellcome, the Bill and Melinda Gates Foundation, and Mastercard.