Baricitinib Therapy in COVID-19

NCT04358614 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-04-24

No results posted yet for this study

Summary

Retrospective study on the efficacy of baricitinib in 12 COVID-19 patients with moderate pneumonia.

Conditions

Interventions

DRUG

Baricitinib 4 MG Oral Tablet

Baricitinib+antiviral therapy administration for 2 weeks

Sponsors & Collaborators

  • Fabrizio Cantini

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-16
Primary Completion
2020-04-05
Completion
2020-04-07

Countries

  • Italy

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04358614 on ClinicalTrials.gov