Official Title
Efficacy of Fingolimod in the Treatment of New Coronavirus Pneumonia (COVID-19)
Brief Summary

Although immune-inflammatory treatment is not routinely recommended to be used for SARS-CoV-2 pneumonia, according to the pathological findings of pulmonary oedema and hyaline membrane formation, timely and appropriate use of immune modulator together with ventilator support should be considered for the severe patients to prevent ARDS development. The sphingosine-1-phosphate receptor regulators Fingolimod (FTY720) is an effective immunology modulator which has been widely used in multiple sclerosis.The aim of this study was to determine whether the efficacy of fingolimod for a novel coronavirus disease (COVID-19).

Withdrawn
Coronavirus Disease (COVID-19)

Drug: Fingolimod 0.5 mg

Each patient in the fingolimod treatment group was given 0.5 mg of fingolimod orally once daily, for three consecutive days

Eligibility Criteria

Inclusion Criteria:

- The patients who were diagnosed with the common type of NCP (including severe risk
factors) and severe cases of new coronavirus pneumonia;

- Aged 18 to 85 years;

- Patients or authorized family members volunteered to participate in this study and
signed informed consent.

Exclusion Criteria:

- Patients with any history of bradyarrhythmia or atrioventricular blocks

- Patients who are participating in other drug clinical trials;

- Pregnant or lactating women;

- ALT / AST> 5 ULN, neutrophils <0.5, platelets less than 50;

- Definite diagnosis of rheumatic immune-related diseases;

- Long-term oral anti-rejection or immunomodulatory drugs;

- Patients with active pulmonary tuberculosis, with definite bacterial and fungal
infections.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 80 Years
Countries
China
Locations

Wan-Jin Chen
Fuzhou, China

First Affiliated Hospital of Fujian Medical University
NCT Number
MeSH Terms
COVID-19
Coronavirus Infections
Fingolimod Hydrochloride