This is an expanded access program (EAP) for eligible participants designed to provide access to fedratinib. Expanded access is only available in markets where fedratinib is not yet approved.
This program is being offered on a patient by patient basis and will require company,
Institutional Review Board/Independent Ethics Committee and Single Patient IND approval.
Drug: Oral Fedratinib
Oral fedratinib administered as directed by treating physician.
Other Name: FEDR
Inclusion Criteria:
Subjects will be considered if they received TG101348, SAR302503 or Fedratinib as a
participant on a clinical trial prior to 31 Jan 2018.
Exclusion Criteria:
Subject is eligible for enrollment in an ongoing clinical trial using Fedratinib or has
been treated with Fedratinib after 31 Jan 2018.
Celgene
Summit, New Jersey, United States
Celgene Medical Information
1-888-771-0141
medinfo@celgene.com