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Completed

NCT Number: NCT04323527

Chloroquine Diphosphate for the Treatment of Severe Acute Respiratory Syndrome Secondary to SARS-CoV2

In December 2019, the Municipal Health Committee of Wuhan, China, identified an outbreak of viral pneumonia of unknown cause. This new coronavirus was called SARS-CoV-2 and the disease caused by that virus, COVID-19. Recent numbers show that 222,643 infections have been diagnosed with 9115 deaths, worldwide. Currently, there are no approved therapeutic agents available for coronaviruses. In this scenario, the situation of a global public health emergency and evidence about the potential positive effect of chloroquine (CQ) in most coronaviruses, including SARS-CoV-1, and recent data on small trials on SARS-CoV-2, the investigators intend to investigate the efficacy and the safety of CQ diphosphate in the treatment of hospitalized patients with severe acute respiratory syndrome in the scenario of SARS-CoV2. Preliminary in vitro studies and uncontrolled trials with low number of patients of CQ repositioning in the treatment of COVID-19 have been encouraging. The main hypothesis is that CQ diphosphate will reduce mortality in 50% in those with severe acute respiratory syndrome infected by the SARS-COV2. Therefore, the main objective is to assess whether the use of chloroquine diphosphate reduces mortality by 50% in the study population. The primary outcome is mortality in day 28 of follow-up. According to local contingency plan, developed by local government for COVID-19 in the State of Amazonas, the Hospital Pronto-Socorro Delphina Aziz, located in Manaus, is the reference unit for the admission of serious cases of the new virus. The unit currently has 50 ICU beds, with the possibility of expanding to 335 beds, if needed. The hospital also has trained multiprofessional human resources and adequate infrastructure. In total, 440 participants (220 per arm) will receive either high dose chloroquine 600 mg bid regime (4x150 mg tablets, every 12 hours, D1-D10) or low dose chloroquine 450mg bid regime (3x150mg tablets + 1 placebo tablet every 12 hours on D1, 3x150mg tablets + 1 placebo followed by 4 placebo tablets 12h later from D2 to D5, and 4 placebo tablets every 12 hours, D6-D10). Placebo tablets were used to standardize treatment duration and blind research team and patients. All drugs administered orally (or via nasogastric tube in case of orotracheal intubation). Both intervention and placebo drugs will be produced by Farmanguinhos. Clinical and laboratory data during hospitalization will be used to assess efficacy and safety outcomes.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospital e Pronto Socorro Delphina Rinaldi Abdel Aziz

Manaus, Amazonas, 69093-415, Brazil

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female participants aged over 18 years old
  • Hospitalized
  • presenting:
  • respiratory rate higher than 24 breathing incursions per minute AND/OR
  • heart rate higher than 125 beats per minute (in the absence of fever) AND/OR
  • peripheral oxygen saturation lower than 90% in ambient air AND/OR
  • shock (defined as mean arterial pressure less than 65 mmHg, requiring vasopressor or oliguria or lowering level of consciousness)

Exclusion criteria

  • None.

Treatment and study plan

Chloroquine diphosphate

Drug

150mg chloroquine diphosphate tablets. Note: Tablets used in the study were Chloroquine Diphosphate (produced by Farmanguinhos/Fiocruz), and the dosing stated in the clinicaltrials.gov refers to chloroquine base (in mg).

Other names: chloroquine

Primary outcomes

  1. Mortality rate reduction of 50% by day 28

    Time frame: 28 days after randomization

    proportion of deaths at day 28 between groups compared

Secondary outcomes

  1. Absolute mortality on days 7 and 14

    Time frame: 7 and 14 days after first dose

    number of deaths at days 7 and 14 between groups compared

  2. Improvement in overall subject's clinical status assessed in standardized clinical questionnaires on days 14 and 28

    Time frame: 14 and 28 days after first dose

    clinical status

  3. Improvement in daily clinical status assessed in standardized clinical questionnaires during hospitalization

    Time frame: during and after intervention, up to 28 days

    clinical status

  4. Duration of supplemental oxygen (if applicable)

    Time frame: during and after intervention, up to 28 days

    supplemental oxygen

  5. Duration of mechanical ventilation (if applicable)

    Time frame: during and after intervention, up to 28 days

    mechanical ventilation

  6. Absolute duration of hospital stay in days

    Time frame: during and after intervention, up to 28 days

    hospitalization

  7. Prevalence of grade 3 and 4 adverse events

    Time frame: during and after intervention, up to 28 days

    adverse events grade 3 and 4

  8. Prevalence of serious adverse events

    Time frame: during and after intervention, up to 28 days

    adverse events

  9. Change in serum creatinine level

    Time frame: during and after intervention, up to 28 days

    increase or decrease in serum creatinine compared to baseline

  10. Change in serum troponin I level

    Time frame: during and after intervention, up to 28 days

    increase or decrease in serum troponin I compared to baseline

  11. Change in serum aspartate aminotransferase level

    Time frame: during and after intervention, up to 28 days

    increase or decrease in serum aspartate aminotransferase compared to baseline

  12. Change in serum CK-MB level

    Time frame: during and after intervention, up to 28 days

    increase or decrease in serum aspartate aminotransferase compared to baseline

  13. Change in detectable viral load in respiratory tract swabs

    Time frame: during and after intervention, up to 28 days

    virus clearance from respiratory tract secretion

  14. Viral concentration in blood samples

    Time frame: during and after intervention, up to 28 days

    viremia in blood detected through RT-PCR

  15. Absolute number of causes leading to participant death (if applicable)

    Time frame: during and after intervention, up to 28 days

    death

Sponsors and collaborators

Lead sponsor

Fundação de Medicina Tropical Dr. Heitor Vieira Dourado

Other

Collaborators

  • Felipe Gomes Naveca
  • Fernando Fonseca de Almeida e Val
  • Gisely Cardoso de Melo
  • Jorge Souza Mendonça
  • Ludmila Abrahão Hajjar
  • Marcus Vinícius Guimarães de Lacerda
  • Maria Paula Gomes Mourão
  • Mayla Gabriela Silva Borba
  • Wuelton Marcelo Monteiro

Registry information

Official study title

Efficacy and Safety of Chloroquine Diphosphate for the Treatment of Hospitalized Patients With Severe Acute Respiratory Syndrome Secondary to SARS-CoV2: a Phase IIb, Double-blind, Randomized Adaptive Clinical Trial

Acronym: CloroCOVID19

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Mar 26, 2020
Registry last updated
Aug 9, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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