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Clinical Trial Summary

The purpose of this Cohort Treatment Plan is to allow access to ruxolitinib for eligible patients diagnosed with severe/very severe COVID-19 illness. The patient's Treating Physician should follow the suggested treatment guidelines and comply with all local health authority regulations. The requesting Treating Physician submitted a request for access to drug (often referred to as Compassionate Use) to Novartis which was reviewed and approved by the medical team experienced with the drug and indication. Please refer to the latest Investigator's Brochure (IB) or approved label for overview of ruxolitinib including: non-clinical and clinical experience, risk and benefits. Novartis will continue to provide any new safety information to the Treating Physician as they emerge.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04337359
Study type Expanded Access
Source Novartis
Contact
Status No longer available
Phase

See also
  Status Clinical Trial Phase
Available NCT04745637 - Managed Access Programs for INC424, Ruxolitinib