Fingolimod in COVID-19
- Registration Number
- NCT04280588
- 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).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Treatment group Fingolimod 0.5 mg -
- Primary Outcome Measures
Name Time Method The change of pneumonia severity on X-ray images 5 day after fingolimod treatment The lesion change on X-ray images from day 5 to baseline
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Wan-Jin Chen
🇨🇳Fuzhou, China