Expanded Access Program of Ponatinib
a study on Chronic Myeloid Leukemia Leukemia Acute Lymphoblastic Leukemia Lymphoma
Summary
- Eligibility
- for people ages 18 years and up (full criteria)
- Location
- at La Jolla, California and other locations
- Dates
- study started
Description
Summary
This protocol will allow expanded access of ponatinib to patients ≥18 years with chronic myeloid leukemia (CML) any phase or Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL) who have failed all available treatment options.
Official Title
Expanded Access Program of Ponatinib (AP24534) for Patients With Refractory Chronic Myeloid Leukemia or Ph+ Acute Lymphoblastic Leukemia
Details
This protocol will allow expanded access of ponatinib to patients ≥18 years with CML or Ph+ALL who have failed all available treatment options. Patients with chronic (CP) or accelerated phase (AP) CML must be previously treated with and resistant or intolerant to imatinib, dasatinib and nilotinib or develop the T315I mutation after any tyrosine kinase inhibitor (TKI) therapy. Patients with blast phase (BP) CML and Ph+ ALL must be previously treated with and resistant or intolerant to imatinib and dasatinib or develop the T315I mutation after any TKI therapy. No formal analysis will be performed on any data obtained. Safety information will be collected and adverse events will be tabulated for reporting purposes only.
Keywords
Chronic Myeloid Leukemia (CML), Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia (Ph+ ALL), Ponatinib, Tyrosine kinase inhibitor, Leukemia, Myeloid Leukemia, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Lymphoid Leukemia, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, Philadelphia Chromosome
Eligibility
You can join if…
Open to people ages 18 years and up
- CP-CML and AP-CML patients previously treated with and resistant or intolerant to imatinib, dasatinib and nilotinib or those who developed the T315I mutation after any TKI therapy. BP-CML and Ph+ ALL patients previously treated with and resistant or intolerant to imatinib and dasatinib or those who developed the T315I mutation after any TKI therapy.
- Patients must be ≥ 18 years old.
- Provide written informed consent.
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
- Men and women of childbearing potential must agree to effective contraception from the time of signing informed consent through the Follow-up Visit, approximately 30 days after last dose of ponatinib.
You CAN'T join if...
Patients are not eligible for participation in the study if they meet any of the following exclusion criteria:
- Are eligible for an ongoing and accessible clinical trial of ponatinib
- Have not adequately recovered from AEs due to agents previously administered
- Require concurrent treatment with immunosuppressive agents, other than corticosteroids prescribed for a short course of therapy.
- Have previously been treated with ponatinib.
- Have significant or active cardiovascular disease, specifically including, but not restricted to:
- Myocardial infarction within 3 months prior to first dose of ponatinib,
- History of clinically significant atrial arrhythmia or any ventricular arrhythmia,
- Unstable angina within 3 months prior to first dose of ponatinib,
- Congestive heart failure within 3 months prior to first dose of ponatinib.
- Have abnormal QTcF (> 450 ms for males or > 470 ms for females)
- Have a significant bleeding disorder unrelated to CML or Ph+ ALL.
- Have a history of pancreatitis or alcohol abuse
- Have elevated amylase or lipase (> 1.5 x ULN for institution) at entry.
- Have inadequate hepatic function or any of the following:
- Total bilirubin > 1.5 x ULN for institution at entry
- Alanine aminotransferase and aspartate aminotransferase > 2.5 x ULN for institution at entry
- Prothrombin time >1.5 x ULN for institution at entry
- Have inadequate renal function or serum creatinine > 2.5 x ULN for institution at entry
- Have uncontrolled hypertriglyceridemia or triglycerides > 450 mg/dL at entry.
- Have malabsorption syndrome or other gastrointestinal illness that could affect absorption of orally administered ponatinib.
- Women who are pregnant or lactating.
- Underwent major surgery within 14 days prior to the first dose of ponatinib.
- Have ongoing or active infection (including known history of human immunodeficiency virus [HIV], hepatitis B virus [HBV], or hepatitis C virus [HCV]).
- Suffer from any condition or illness that, in the opinion of the Investigator would compromise patient safety or interfere with the evaluation of the safety of the study drug.
Locations
- Moores UCSD Cancer Center, Site #165
La Jolla California 92093 United States - Southern California Permanente Medical Group, Site #161
San Marcos California 92069 United States
Details
- Status
- not accepting new patients
- Start Date
- Sponsor
- Ariad Pharmaceuticals
- ID
- NCT01592136
- Study Type
- Expanded Access
- Last Updated