Viewing Study NCT04334044



Ignite Creation Date: 2024-05-06 @ 2:30 PM
Last Modification Date: 2024-10-26 @ 1:32 PM
Study NCT ID: NCT04334044
Status: COMPLETED
Last Update Posted: 2021-07-07
First Post: 2020-04-01

Brief Title: Treatment of SARS Caused by COVID-19 With Ruxolitinib
Sponsor: Grupo Cooperativo de Hemopatías Malignas
Organization: Grupo Cooperativo de Hemopatías Malignas

Study Overview

Official Title: Treatment of Severe Acute Respiratory Syndrome Caused by COVID-19 With Ruxolitinib
Status: COMPLETED
Status Verified Date: 2021-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In December 2019 a new virus emerged in Wuhan China rapidly becoming a pandemic with registered cases above 800000 around the world The virus is now known as SARS-CoV2 calling its disease coronavirus-19 or COVID-19 The mortality of the virus has been reported around 2-10 and its causes because of the proinflammatory immune response generated on the host The cytokines involved in the immune response to COVID-19 are IL-1 IL-2 IL4 IL-6 IL-10 IL-12 IL-13 IL-17 GCSF MCSF IP-10 MCP-1 MIP-1α HGF IFN-γ y TNF-α

Ruxolitinib is an inhibitor of JAK 12 which is responsable for multiple cellular signals including the proinflammatory IL-6 Ruxolitinib works as and immunomodulator decreasing the cytotoxic T lymphocytes and increasing the Treg cells

This study is intended to stop the disregulated immune response caused by COVID-19 that generates the pneumonia and subsequent severe acute respiratory syndrome
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None