Chemoprevention Clinical Trial of COVID-19: Hydroxychloroquine Post Exposure Prophylaxis

Type of study and design Prospective, Randomized, open-label, three-arm, parallel, controlled adaptive phase II/III clinical trial in which subjects will be randomly assigned in a 1:1:1 ratio as per the following: Arm 1 Arm 2 Arm 3 Day 1 HCQ 400 mg (twice daily) HCQ 200 mg (twice daily) Standard measurements of the country until the end of the participation in the study Day 2 HCQ 400 mg (once daily) HCQ 200 mg (once daily) Day 3 HCQ 400 mg (once daily) HCQ 200 mg (once daily) Day 4 HCQ 400 mg (once daily) HCQ 200 mg (once daily) Day 5 HCQ 400 mg (once daily) HCQ 200 mg (once daily) Amount needed: Plaquenil 200mg: 558 tables per protocol. 42 tablets are needed as preserved supply: total 600 tables. Randomisation Subjects who meet the eligibility criteria at the study locations will be invited to take part in the study. Participants will be randomly assigned to the treatment arms. Index cases will be used for the assignment of contacts. For example, number 1,4,7, 9. will be on arm 1, number 3, 5, 10.etc. will be in arm 2, number 2,6, 8, etc. will be in arm 3. All close contacts of the same index case will be allocated to the same arm. This would allow more valid results through prevention of potential further exposure to the virus mainly for the control arms, who are expected to have higher incidence of the disease. Blinding This clinical trial is open-label. The study does not compare multiple medicinal products; it also does not include the use of a placebo product, as it is a Proamtic clinical trial. Study procedures and evaluations Baseline assessment * Medical history * Inquiry about previous history of G6PD * Check for contraindications * Vital signs * Physical examination * RT-PCR * IgM, IgG AB for SARS-Cov-2 * Hematology * Biochemistry * Urinalysis * Retinopathy * Pregnancy test * ECG * Retinopathy screening During follow-up visits subjects will assessed for: * Random glucose level * Vital signs * Assessment of study intervention adherence * Assessment of adverse events. * ECG * Retinopathy screening Study schedule Sampling technique: This adaptive phase II/III clinical trial will be conducted in two sites in Tunisia. The main study is planned in 2 sites in Tunisia. As soon as a new subject in identified, he/she will be consented for reaching his contacts according to Eligibility criteria. The research team within 48 hours of index case identification will call his/her contacts who fulfil below criteria for participation in the trial. All potential participants will be tested using RT-PCR and IgM and IgG antibodies to rule out current or previous disease status. Results will be obtained on the same day and before consenting for taking part in the study. Subjects positive for COVID-19 will be referred to local authorities for treatment according to their protocols. We will follow multistage sampling technique in involved countries. Samples will be stratified by gender and then follow simple random sampling process. Screening Before carrying out any procedure in this study, subjects will be provided "subject information and consent form". The study will be thoroughly explained and all questions will be answered to the satisfaction of the subject. Subjects will be given enough time to think about their participation through and inquire about any detail that may influence the decision. Consent procedure will be carried out by the clinical investigator \& delegated clinical staff. Neither the investigator nor the study staff will coerce or unduly influence subjects to participate or to continue to participate against their will. Prior to the subject's participation, the subject will personally sign \& date the consent form, along with one witness at least \& the principal investigator (the principal investigator may delegate the clinical investigator to sign the ICF whenever needed). Enrollment (Baseline) All potential participants will be tested using RT-PCR and IgM and IgG antibodies to rule out current or previous disease status. Results will be obtained on the same day and before consenting for taking part in the study. Subjects positive for COVID-19 will be referred to local authorities for treatment according to their protocols. Only subjects eligible for this study will be enrolled. Refer to section 5 for eligibility criteria. Informed consent, , demographics, vital signs, Medical History and contraindications, physical examination,hematology, KFT, LFT, urinalysis,IgM and IgG antibodies for SARS-CoV-2, RT-PCR, Pregnancy test, ECG, Retinopathy screening, Blood Glucose, dosing, Adverse event review During screening and follow-up visits, subjects will be examined and vital signs will be taken with relevant medical history taken to determine the lack of contraindication of the use the IMP and the achievement of the inclusion criteria Laboratory evaluations Laboratory evaluations will be conducted as per Table 6.1 of visits and procedures elaborated on table 6.1. Safety considerations Methods and timing for assessing, recording, and analysing safety parameters Adverse events The study period during which adverse events must be reported is normally defined as the period from the initiation of any study procedures to the end of the study treatment follow-up. At each contact with the subject, the Clinical Investigator will seek information on adverse events by specific questioning and, as appropriate, by examination. Information on all adverse events will be recorded immediately in the source document, and also in the appropriate adverse event module of the case report form (CRF). All adverse events occurring during the study period will be recorded. The clinical course of each event will be followed until resolution, stabilization, or until it has been determined that the study treatment or participation is not the cause. Serious adverse events that are still ongoing at the end of the study period will be followed up to determine the final outcome. Any serious adverse event that occurs after the study period and is considered to be possibly related to the study treatment or study participation should be recorded and reported immediately. The AE report will include the intensity, severity, duration of the event. It will also explain how the case was managed. At the end of the study, all records and follow up forms of AEs/ADRs/SAEs/SADRs will be enlisted in the final report. 4 Discontinuation criteria 4.1 Participant's premature termination The reason for participant's premature termination will be documented on the appropriate page of the CRF and specified which of the following possible reasons were responsible for the study premature termination: * Serious Adverse Event / SUSAR * Participant's consent withdrawal * Inappropriate enrolment * Development of exclusion criterion * Protocol deviation: as described below: * Such as not taking study treatment on time or the prescribed dose more than one time. * Decline PCR test at baseline or during the follow-up * Decline ECG or ophthalmoscopy exams. * Migrated/moved from the study area * Lost to follow-up. A 'lost to follow-up' is any participant who completed all protocol specific procedures up to the administration of the investigational product or intervention, but was then lost during the study period to any further follow-up, with no safety information and no efficacy endpoint data ever became available. It is vital to collect safety data on any participant discontinued because of an AE or SAE. In any case, every effort must be made to undertake protocol-specified safety follow-up procedures. If voluntary withdrawal occurs, the participant should be asked to continue scheduled evaluations, complete an end-of-study evaluation, and be given appropriate care under medical supervision until the symptoms of any AE resolve or the participant's condition becomes stable. 5 Statistical considerations Following an adaptive seamless phase II/III design assuming 60% efficacy (an odds ratio of about 0.3) of hydroxychloroquine in reducing COVID-19 infections for primary contacts, and reported secondary attack rate of 35% (incidence amongst close contacts), Liu Y., et.al. 90% power, a confidence level of 95% and 10% loss to follow-up, 31 COVID-19 contacts are needed in each arm for phase II totaling 93 contacts for the three arms. The primary endpoints of this study are observed COVID-19 infection and observed ADRs. Descriptive statistics including means, frequencies and proportions will be used to summarize collected contacts data. Incidence of the primary endpoints will be reported as well. All summaries will be provided for the three study arms. Chi-squared test will be used to compare incidence levels of the primary endpointsacross the three study arms. To examine for associations among categorical contacts attributes, Chi-squared and Fishers exact tests whenever appropriate will be used.When needed, ANOVA will be used to test for significant differences among numerical attributes.Logistic Regression techniques with stepwise selection method will be used to identify significant predictors of the primary endpoints Intention to treat analysis will be followed in this clinical trial Data handling and record keeping Source documents and access to source data The Principal Investigators will maintain appropriate medical and research records for this study in compliance with the principles of good clinical practice and regulatory and institutional requirements for the protection of confidentiality of participants. The study team members will have access to records. Authorised representatives of the sponsor, the ethics committee(s) or regulatory bodies may inspect all documents and records required to be maintained by the investigator for the purposes of quality assurance reviews, audits, inspections, and evaluation of the study safety and progress. This will include, but not limited to, medical records (office, clinic, or hospital) for the participants in this study. The clinical study site will permit access to such records. Missing data will be reported as missing indicating the reasons where applicable. Protocol deviations A protocol deviation is any noncompliance with the clinical trial protocol, good clinical practice (GCP), or other protocol-specific requirements. If a deviation from, or a change of, the protocol is implemented to eliminate an immediate hazard(s) to trial participant without prior ethics approval, the PI or designee will submit the implemented deviation or change, the reasons for it, and, if appropriate, the proposed protocol amendment(s) as soon as possible to the relevant ethics committee(s) for review and approval and to the sponsor for agreement. The PI or designee will document and explain any deviation from the approved protocol on the CRF, where appropriate, and record and explain any deviation in a file note or deviation form that will be maintained as an essential document. Deviations from the protocol, GCP or trial specific requirements that might have an impact on the conduct of the trial or the safety of participants will be reported within 5 working days to the sponsor and relevant EC, as appropriate. Ethical considerations The investigator will ensure that this study is conducted in full conformity with the principles set forth in the ICH Harmonised Tripartite Guideline for Good Clinical Practice and the Declaration of Helsinki in its current version, whichever affords the greater protection to the participants. Rationale for participants election Study population will be males and females aged 18-65 years (non-pregnant and non-lactating) with primary exposure to COVID-19 patients. The study is proposed to be conducted in Tunisia. Financing and insurance All subjects will be covered by insurance throughout the study and in case of an injury to health caused by the trial.