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Expanded Access for Fedratinib

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ClinicalTrials.gov Identifier: NCT03723148
Expanded Access Status : Available
First Posted : October 29, 2018
Last Update Posted : October 29, 2018
Sponsor:
Information provided by (Responsible Party):
Celgene

Brief Summary:
This is an expanded access program (EAP) for eligible participants designed to provide access to Fedratinib.

Condition or disease Intervention/treatment
Myelofibrosis Drug: Oral Fedratinib

Study Type : Expanded Access
Expanded Access Type : Individual Patients
  See clinical trials of the intervention/treatment in this expanded access record.
Official Title: Expanded Access for Fedratinib



Intervention Details:
  • Drug: Oral Fedratinib
    Oral fedratinib administered as directed by treating physician.
    Other Name: FEDR

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03723148


Contacts
Contact: Celgene Medical Information 1-888-771-0141 medinfo@celgene.com

Locations
United States, New Jersey
Celgene
Summit, New Jersey, United States, 07901
Sponsors and Collaborators
Celgene

Responsible Party: Celgene
ClinicalTrials.gov Identifier: NCT03723148     History of Changes
Other Study ID Numbers: FEDR
First Posted: October 29, 2018    Key Record Dates
Last Update Posted: October 29, 2018
Last Verified: October 2018

Keywords provided by Celgene:
Expanded Access
Compassionate Use

Additional relevant MeSH terms:
Primary Myelofibrosis
Myeloproliferative Disorders
Bone Marrow Diseases
Hematologic Diseases