Safety and Efficacy of BKM120 in Patients With Metastatic Non-small Cell Lung Cancer
Status: | Completed |
---|---|
Conditions: | Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | May 2011 |
End Date: | October 2014 |
An Open Label Two-stage Study of Orally Administered BKM120 in Patients With Metastatic Non-small Cell Lung Cancer With Activated PI3K Pathway
The purpose of this two-stage phase II study is to assess the efficacy of BKM120, as
measured by determining the progression free survival (PFS), in patients with pretreated
metastatic Non-small Cell Lung Cancer (NSCLC) that exhibits PI3K pathway activation. BKM120
will be investigated in two groups of NSCLC patients according to the histology of the
cancer: squamous and non-squamous.
measured by determining the progression free survival (PFS), in patients with pretreated
metastatic Non-small Cell Lung Cancer (NSCLC) that exhibits PI3K pathway activation. BKM120
will be investigated in two groups of NSCLC patients according to the histology of the
cancer: squamous and non-squamous.
Inclusion Criteria:
- Histologically confirmed NSCLC with activated PI3K pathway
- Progressive disease after prior systemic antineoplastic treatment(s) for advanced
NSCLC
- Archival or fresh tumor biopsy must be available for profiling
- Measurable and/or non-measurable disease as per RECIST 1.1 criteria
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
- Adequate organ function as assessed by laboratory tests
Exclusion Criteria:
- Patient has received previous treatment with PI3K inhibitors
- Patient with squamous NSCLC has received more than one line of chemotherapy treatment
for metastatic disease; patient with non-squamous NSCLC has received more than two
lines of systemic antineoplastic treatment for metastatic disease
- Uncontrolled or symptomatic CNS metastases
- Concurrent use of any other approved or investigational antineoplastic agent
- Radiotherapy ≤ 28 days prior to starting study drug
- Major surgery within 28 days prior to starting study drug
- History of clinically significant cardiac dysfunction, mood disorders, or poorly
controlled diabetes mellitus
- Current treatment with medication that has a known risk to prolong the QT interval or
inducing Torsades de Pointes
- Impairment of gastrointestinal (GI) function
- Chronic treatment with steroids or another immunosuppressive agent.
- Concurrent severe and/or uncontrolled medical condition
- Currently receiving Warfarin or another coumarin derivative
- Known history of HIV infection
- Sensory neuropathy with functional impairment (CTC grade 2 neuropathy, regardless of
causality)
- Pregnancy, lactation, or breastfeeding
- Woman of child-bearing potential
Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
33
sites
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Dallas, Texas 75390
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Morristown, New Jersey 07962
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Oklahoma City, Oklahoma 73104
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Worcester, Massachusetts 01608
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