Masitinib Combined With Isoquercetin and Best Supportive Care in Hospitalized Patients With Moderate and Severe COVID-19

Last updated: February 3, 2023
Sponsor: AB Science
Overall Status: Active - Recruiting

Phase

2

Condition

Covid-19

Sars-cov-2

Treatment

N/A

Clinical Study ID

NCT04622865
AB20001
2020-001635-27
  • Ages > 18
  • All Genders

Study Summary

Study objective is to evaluate the efficacy of the combination of masitinib and isoquercetin in adult hospitalized patients with moderate and severe COVID-19.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Has laboratory-confirmed SARS-CoV-2 infection

  • Hospitalized patients for the treatment of COVID pneumopathy

  • Patients not requiring ICU at admission with moderate and severe pneumopathy according to the OMS Criteria of severity of COVID pneumopathy.

Study Design

Total Participants: 200
Study Start date:
June 01, 2020
Estimated Completion Date:
December 31, 2023

Study Description

COVID-19 is a respiratory disease caused by a novel coronavirus (SARS-CoV-2) that is associated with substantial morbidity and mortality. There is currently no vaccine to prevent COVID-19 or infection with SARS-CoV-2 or therapeutic agent to treat COVID-19.

Many patients with moderate and severe COVID-19, develop a "cytokine storm" that leads to severe pulmonary inflammation and various thrombotic events associated with acute respiratory distress syndrome (ARDS) and potentially death. The combination of masitinib and isoquercetin may prevent the development of these two complications. Masitinib is a potent blocker of mast cells and macrophages that are contributors to the cytokine storm. Isoquercetin inhibits disulfide isomerase (PDI), an enzyme directly involved in the formation of clots, and also decreases D-Dimer, a predictor of COVID-19 thrombosis severity.

The primary objective of this study is to evaluate efficacy of the masitinib and isoquercetin combination in moderate and severe COVID-19 patients. The primary endpoint is subject clinical status at day 15, using a 7-point ordinal scale that is defined as follows: 1. Not hospitalized, no limitations on activities; 2.Not hospitalized, limitation on activities; 3. Hospitalized, not requiring supplemental oxygen; 4. Hospitalized, requiring supplemental oxygen; 5. Hospitalized, on non-invasive ventilation or high flow oxygen devices; 6. Hospitalized, on invasive mechanical ventilation or ECMO; 7. Death.

Connect with a study center

  • Centre Hospitalier du Pays d'Aix

    Aix-en-Provence,
    France

    Active - Recruiting

  • Le Tripode, Groupe hospitalier Pellegrin CHU de Bordeaux

    Bordeaux,
    France

    Active - Recruiting

  • CHU Clermont-Ferrand: Site Gabriel-Montpied

    Clermont-Ferrand,
    France

    Active - Recruiting

  • Hopital Nord, AP-HM

    Marseille,
    France

    Active - Recruiting

  • CHR Orleans, Hopital de la Source

    Orléans,
    France

    Active - Recruiting

  • Hopital Larrey, CHU du Toulouse

    Toulouse,
    France

    Active - Recruiting

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