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NCT03592576 Clinical Trial

Expanded Access to Navitoclax

Myelofibrosis Clinical Trial

Official title:
Expanded Access to Navitoclax

Clinical Trial Details — Status: No longer available

Administrative data
NCT number NCT03592576
Other study ID # C19-199
Secondary ID C19-922
Status No longer available
Phase
First received
Last updated

Study information
Verified date May 2024
Source AbbVie
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial 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. 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.

Recruitment information / eligibility
Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 4 Years and older
Eligibility

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Navitoclax
Tablet, Oral
• Venetoclax
Tablet, Oral

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
AbbVie
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