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Expanded Access to Navitoclax

Expanded Access to Navitoclax

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT03592576
Enrollment
Unknown
Registered
2018-07-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Lymphocytic Leukemia (ALL), Lymphoblastic Lymphoma, Myelofibrosis

Keywords

Expanded Access, Pre-approval Access, Compassionate Use, Special Access Program, Named Patient Basis, Special Access Scheme

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. 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.

Interventions

DRUGNavitoclax

Tablet, Oral

DRUGVenetoclax

Tablet, Oral

Sponsors

AbbVie
Lead SponsorINDUSTRY

Eligibility

Age
4 Years to No maximum
Healthy volunteers
No

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026