Covid19
Conditions
Brief summary
Chloroquine and hydroxychloroquine are two antimalarial drugs that are also used in autoimmune diseases. Chloroquine analogs have been shown to inhibit endosome acidification and exhibit nonspecific antiviral activity at high micromolar concentration in vitro against a wide range of emerging viruses (HIV, dengue, hepatitis C, chikungunya, influenza, Ebola, SARS, and MERS ). virus) and more recently COVID-19. On the other hand, azithromycin is a macrolide antibiotic indicated for infections caused by sensitive pathogens, but which in combination with Hydroxychloroquine has shown a synergistic effect against the SARS-CoV-2 virus. International studies show the lack of beneficial effect in hospitalized or mechanically ventilated patients. Referring that because these medications reduce the in case of having a beneficial effect it would be in the early onset, to avoid inflammation (cytokine storm), and thus prevent hospitalizations. The present study focuses on characterizing the possible synergy of the fixed combination of hydroxychloroquine associated with azithromycin in the treatment of Covid-19 from mild to moderate manifestations. Three treatment schemes are proposed with a 10-day follow-up, a) the fixed combination of Hydroxychloroquine / Azithromycin (combination of interest), b) Hydroxychloroquine (active comparison group) and c) non-active control group, using placebo. A group of patients between 18 and 75 years old is considered, who may or may not present other comorbidities. Follow-up will be carried out through quantification of viral load, evaluation of the systemic inflammatory state, changes in clinical manifestations and possible effect on the reduction of hospitalizations. Therefore, it is proposed to carry out the following project. objective To determine the efficacy and safety of Hydroxychloroquine / Azithromycin fixed combination compared to Hydroxychloroquine or placebo in outpatients with Research design: Phase II, multicenter, prospective, randomized, parallel, longitudinal, double-blind study. Medications to use Group 1. Fixed combination of Hydroxychloroquine with Azithromycin 200 mg / 250 mg one tablet every 12 hours for five days and continue with Hydroxychloroquine 200 mg one tablet every 12 hours for 5 more days. Group 2. Hydroxychloroquine 200 mg, one tablet every 12 hours for ten days. Group 3. Placebo one tablet every 12 hours for ten days.
Interventions
DRUGHydroxychloroquine with Azithromycin
Fixed combination of Hydroxychloroquine with Azithromycin 200 mg / 250 mg one tablet every 12 hours for five days and continue with Hydroxychloroquine 200 mg one tablet every 12 hours for 5 more days.
Sponsors
Ultra Laboratorios SA. de CV.
Coordinación de Investigación en Salud, Mexico
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Have given the signed informed consent form. * Confirmed diagnosis of COVID-19 infection by PCR with mild symptoms. * Patients who attend the primary care respiratory care module in the participating units and who have symptoms suggestive of COVID-19, who comply with the current operational definition. * With or without comorbidities such as hypertension, controlled diabetes mellitus, cardiovascular or respiratory diseases. * Controlled diabetes will be considered to be that which is evidenced by results of glycosylated hemoglobin less than 7% in the last 3 tables, whether it is reported in your beneficiary file or by external laboratory results. * Electrocardiogram (ECG) normal or with variations without clinical relevance, with QT interval \<450 ms. * No contraindication to study drugs (history of hypersensitivity to study drugs, including macrolides, patients with renal failure (eGFR \<40 mL / min) or on renal replacement therapy, patients with a history of retinopathy or macular degeneration.
Exclusion criteria
* Patients who are participating in studies with investigational drugs. * Pregnancy or breastfeeding. * Type 1 diabetes * % Type II diabetes mellitus with glycated hemoglobin greater than 7%. * Patients requiring hospitalization or assisted mechanical ventilation * Cardiac disorders with cardiac conduction delay (QT segment ≥ 450 ms
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Hospitalization | 15 days | Being admitted for hospitalization |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Viral load | 0 and 14 days | Measured by RT-PCR |
| Clinical safety | 21 days | any adverse event |
Countries
Mexico
Outcome results
None listed