A Study to Evaluate Effectiveness and Safety of Ponatinib in Patients With BCR-ABL Positive ALL in Standard Clinical Practice in Europe - "POSEIDON"

Incyte

Status: Withdrawn

Conditions: BCR-ABL Positive Acute Lymphoblastic Leukemia

Study type: Observational

Funder types: Industry

Identifiers

NCT03515785

INCB-DEMA-ALL-401

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness and safety of ponatinib (Iclusig®) in patients with BCR-ABL positive acute lymphoblastic leukemia (ALL) in standard clinical practice in Europe.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients with BCR-ABL (Ph+) positive ALL who are initiating Iclusig®, or for whom Iclusig® was initiated after January 2015.
• Patients who have the ability to understand the requirements of the study and provide written informed consent to comply with the study data collection procedures.

Exclusion criteria

• Patients previously treated with investigational ponatinib.
• Patients who are pregnant and/or breastfeeding.
• Concurrent treatment with another tyrosine kinase inhibitor for Ph+ALL.

Trial design

0 participants in 1 patient group

Ph+ ALL Patients

Description:

Patients with Ph+ ALL being treated with Iclusig®.