BKM120 as Second-line Therapy for Advanced Endometrial Cancer
Status: | Completed |
---|---|
Conditions: | Cervical Cancer, Cancer, Cancer, Endometrial Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/30/2013 |
Start Date: | February 2011 |
End Date: | April 2013 |
Contact: | Novartis Pharmaceuticals |
Phone: | +1(800)340-6843 |
A Phase II, Single-arm Study of Orally Administered BKM120 as Second-line Therapy in Patients With Advanced Endometrial Carcinoma
This is a prospective multi-center, open-label, single arm, Phase II study to investigate
the safety and efficacy of BKM120 in patients with advanced endometrial carcinoma whose
disease progressed on or after a first-line antineoplastic treatment. Patients will receive
BKM120 orally at a dose of 100 mg/day. Availability of tumor specimen (either archival
tissue or a fixed fresh biopsy) is mandatory for assessment of the PI3K
(Phosphatidylinositol 3 Kinase (PI3K) pathway activation status.
Inclusion Criteria:
- ECOG (Eastern Cooperative Oncology Group) performance status ≤ 2
- histologically confirmed diagnosis of advanced endometrial carcinoma with available
tissue specimen for identification of PI3K pathway activation (archival tissue or a
fixed fresh biopsy)
- one prior line of antineoplastic treatment with a cytotoxic agent
- objective progression of disease after prior treatment and at least one measurable
lesion as per RECIST criteria
- adequate bone marrow and organ function
Exclusion Criteria:
- previous treatment with PI3K and/or mTOR inhibitors
- symptomatic CNS metastases
- concurrent malignancy or malignancy within 3 years of study enrollment
- Active mood disorder as judged by investigator or medically documented history of
mood disorder (e.g. major depressive episode, bipolar disorder, obsessive-compulsive
disorder, schizophrenia, etc.), ≥ CTCAE grade 3 anxiety
- pelvic and/or para-aortic radiotherapy ≤ 28 days prior to enrollment in the study
- poorly controlled diabetes mellitus (HbA1c > 8 %)
- history of cardiac dysfunction or active cardiac disease as specified in the protocol
- impairment of gastrointestinal (GI) function or GI disease that may significantly
alter the absorption of BKM120
Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
22
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials