Covid19, SARS-CoV Infection
Conditions
Keywords
Nitazoxanide, Sofosbuvir/Daclatasvir, COVID-19, SARS-CoV-2
Brief summary
This is a randomised, multi-center, open label, adaptive, exploratory trial to assess the efficacy of two different drug regimens in terms of preventing symptomatic COVID-19 disease in healthcare workers at high risk of exposure to SARS-CoV-2. The trial will compare two different experimental medication arms to the control arm comprising the use of standard personal protective equipment (PPE) with no additional pharmacological intervention.
Detailed description
This is a randomised, multi-center, open label, adaptive, exploratory trial to assess the efficacy of two different drug regimens in terms of preventing symptomatic COVID-19 disease in healthcare workers at high risk of exposure to SARS-CoV-2. The trial will compare two different experimental medication arms to the control arm comprising the use of standard personal protective equipment (PPE) with no additional pharmacological intervention. Volunteers will be recruited from participating institutions and community healthcare workers (CHWs) that are responsible for collecting swabs for PCR detection of SARS-CoV-2. Up to 1950 (or 2130 pending funding) eligible participants will be randomised in a 1:1:1 ratio to one of the investigational arms. Participants will be followed until 65 PCR and serology-confirmed, SARS-CoV-2 infections are identified in the control arm (or 165 in the entire study cohort). For each episode of PCR-confirmed COVID-19 disease, data on self-reported symptoms (modified Flu-PRO) and their duration, and an investigator-assessed severity score (WHO Ordinal Scale for Clinical Improvement) will be recorded. Data on self-reported symptoms and duration will also be collected for other all-cause acute respiratory illnesses. Safety and tolerability of each arm will be assessed through adverse event reporting. Participants who develop COVID-19 disease will have their IMP discontinued but will be followed up in the study until the completion of the trial, where possible. Multiple, discrete occurrences of COVID-19 disease could therefore be identified in a single participant. Additional arms may be added, or existing ones substituted, should new potential agents be identified or other combinations for prophylaxis be proposed. A formal amendment will be documented should this be considered.
Interventions
DRUGNitazoxanide
Nitozoxanide 1 tablet (500 mg) taken 12-hourly with food for the first week, followed by 2 tablets (1000 mg) taken 12-hourly with food thereafter. (Participants that fail to tolerated the 1000 mg 12-hourly dose may revert back to the lower dose.)
Sofosbuvir/daclatasvir 400mg/60 mg sofosbuvir/daclatasvir fixed dose combination 1 tablet daily
Sponsors
University of Witwatersrand, South Africa
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes
Inclusion criteria
1. Age ≥18 years of age, inclusive, at the time of signing the informed consent. 2. Willing and able to provide informed consent via an electronic process. 3. Healthcare worker employed at a participating institution that has been identified as high-risk for SARS-CoV-2 exposure (may include doctors, nurses, nurse aids, radiographers, physiotherapists, phlebotomists, technicians, porters, cleaners, laboratory or other personnel identified as being at high risk of exposure), CHW involved in the collection of samples for the identification of SARS-CoV-2 through PCR, and inner city inhabitants at high risk for SARS-CoV-2 exposure due to the nature of their work and frequent use of public transport (may include essential services employees such as fire fighters, law enforcement officers, grocery store employees; and non healthcare workers using public transport at least three times a week). 4. Women of reproductive potential must be using a highly effective method of contraception prior to enrolment or must be willing to start a method at enrolment and continue its use throughout the duration of the study. 5. Body weight ≥45 kg. 6. Access to reliable video conference, telephone, direct/text messaging, or other device permitting real-time, reliable information transfer.
Exclusion criteria
1. Pregnant or lactating women. 2. PCR and/or serology confirmed SARS-Cov-2 infection at screening. 3. Current symptoms of COVID-19 disease (including, but not limited to, fever or chills, cough, myalgia, sore throat, shortness of breath, or new onset of anosmia or ageusia, or diarrhea). 4. Self-reported presence or history of any of the following conditions: * Chronic kidney disease (Stage IV or receiving dialysis) * Cirrhosis (Child-Pugh Class B or greater) * Porphyria cutanea tarda. 5. Currently on treatment for epilepsy or other seizure disorder. 6. Currently on treatment with a protease inhibitor-based antiretroviral regimen, or efavirenz, or on treatment with amiodarone, carbamazepine, phenobarbitone, phenytoin, primidone, rifampicin,St. John's wort or any herbal products which may potentially decrease the concentration of the IMP. 7. Known hypersensitivity or specific contraindications to the use of any of the active drugs in the treatment arms or similar compounds. 8. Current enrolment in another COVID-19 prevention trial. 9. History of alcohol abuse within the last 6 months. 10. Having history or have risk factors for brady-arrhythmias (those with undiagnosed cardiac conditions). 11. History of malignancies in the last 5 years, excluding in-situ or non-invasive malignancies. 12. Concurrent or recent (within 3 months) participation in other research with a compound likely to interfere with any of the investigational products. 13. Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of drugs, or which may jeopardize the safety of the volunteer or the objectives of the study. The Investigator should make this determination in consideration of the volunteer's medical history. 14. Inability or unwillingness to be followed up for the study period. 15. Personnel (e.g. investigator, sub-investigator, research assistant, pharmacist, study coordinator or anyone mentioned in the delegation log) directly involved in the conduct of the study. (Personnel employed at a study site, but not directly involved in the conduct of the study, who would like to participate in the study, may only do so if they are enrolled in the study through a different site at which they are not employed.) 16. Participant is judged by the Investigator to be at significant risk of failing to comply with the provisions of the protocol as to cause harm to self or seriously interfere with the validity of the study results. 17. Confirmed vaccination against SARS-Cov-2.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of SARS-CoV-2 infections | 6 months | Number of SARS-CoV-2 infection (COVID-19) confirmed by PCR and/or serology. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Maximum score on WHO Ordinal Scale | 6 months | Maximum score on WHO Ordinal Scale for Clinical Improvement for each symptomatic infection. Score of 0 being uninfected and a score of 8 being dead. |
| Time to onset of SARS-CoV-2 infection | 6 months | Time to onset of SARS-CoV-2 infection (COVID-19) confirmed by PCR and/or serology |
| Duration of symptoms | 6 months | Duration of symptoms for each symptomatic infection |
| Number of asymptomatic SARS-CoV-2 infections | 6 months | Number of asymptomatic • Asymptomatic SARS-CoV-2 infection suggested by serological outcome |
| Peak score on modified Flu PRO | 6 months | Peak score on modified Flu-PRO during each symptomatic infection. 37-item questionairre assessing the severity of flu like symptoms one a scale of 0 - not at all to 5 - very much. |
| Number of symptomatic SARS-CoV-2 infections | 6 months | Number of symptomatic SARS-CoV-2 infection (COVID-19) confirmed by PCR and/or serology |
Countries
South Africa
Outcome results
None listed