Expanded Access to Venetoclax
Sponsor
AbbVie (Industry)
Overall Status
Available
CT.gov ID
NCT03123029
Collaborator
(none)
Study Details
Study Description
Brief Summary
This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to Venetoclax prior to approval by the local regulatory agency. Availability will depend on territory eligibility. 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.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
Study Design
Study Type:
Expanded Access
Official Title:
Expanded Access to Venetoclax
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
The participant must not be eligible for a venetoclax clinical trial.
-
Pediatric participants may be evaluated on a case by case basis.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- AbbVie
Investigators
- Study Director: ABBVIE INC., AbbVie
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
AbbVie
ClinicalTrials.gov Identifier:
NCT03123029
Other Study ID Numbers:
- C16-431
- C19-920
First Posted:
Apr 21, 2017
Last Update Posted:
Mar 29, 2022
Last Verified:
Mar 1, 2022
Keywords provided by AbbVie
Additional relevant MeSH terms: