Expanded Access to Navitoclax

NCT ID: NCT03592576

Last Updated: 2024-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NO_LONGER_AVAILABLE

Study Classification

EXPANDED_ACCESS

Brief Summary

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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.

Detailed Description

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Conditions

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Myelofibrosis Acute Lymphocytic Leukemia (ALL) Lymphoblastic Lymphoma

Interventions

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Navitoclax

Tablet, Oral

Intervention Type DRUG

Venetoclax

Tablet, Oral

Intervention Type DRUG

Other Intervention Names

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ABT-263 Venclexta ABT-199 GDC-0199

Eligibility Criteria

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Minimum Eligible Age

4 Years

Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

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AbbVie

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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C19-922

Identifier Type: OTHER

Identifier Source: secondary_id

C19-199

Identifier Type: -

Identifier Source: org_study_id

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