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AbbVie

Expanded Access to Navitoclax

Official Title: 
Expanded Access to Navitoclax
Brief Summary: 
This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to navitoclax prior to approval by the local regulatory agency. Availability will depend on territory eligibility. Participating sites will be added as they apply for and are approved for the EAP. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.
Available
EA Type
Individual Patients
Myelofibrosis, Acute Lymphocytic Leukemia (ALL), Lymphoblastic Lymphoma, Thyroid Cancer

Drug: Navitoclax
tablet
Other Name: ABT-263

Eligibility Gender: 
All
Eligibility Age: 
Minimum: 18 Years
Contacts: 

ABBVIE CALL CENTER
847.283.8955
abbvieclinicaltrials@abbvie.com

AbbVie Inc.
Study Director
AbbVie

EA Number: 
Keywords: 
Expanded Access, Pre-approval Access, Compassionate Use, Special Access Program, Named Patient Basis, Special Access Scheme
MeSH Terms: 
Leukemia, Lymphoid, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Thyroid Neoplasms, Primary Myelofibrosis, Navitoclax
Disclaimer:
Expanded Access program information for companies listed in the Expanded Access Company Directory is pulled daily from ClinicalTrials.gov, a resource provided by the National Institutes of Health in cooperation with the U.S. Food and Drug Administration. Click here for more information about ClinicalTrials.gov.