Ruxolitinib Managed Access Program (MAP) for Patients Diagnosed With Severe/Very Severe COVID-19 Illness
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT04337359
- Status
- No Longer Available
Conditions
- Severe/Very Severe COVID-19 Illness
Eligibility Criteria
- Sex
- ALL
- Age
- 6 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ruxolitinib — DRUG5 mg. Tablet
Study Details
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.
Key Dates
- Status verified
- Jan 2021