A Phase I/II Study of BEZ235 in Patients With Advanced Solid Malignancies Enriched by Patients With Advanced Breast Cancer

Inclusion Criteria:

[Single agent dose escalation arm]: Patients with histologically-confirmed, advanced unresectable solid tumors including CS patients who have progressed on (or not been able to tolerate) standard therapy within three months before screening visit or for whom no standard anticancer therapy exists.

[Combination part]: Patients with metastatic HER2+ Breast Cancer, after failure of trastuzumab treatment. Eligible patients will have to have tumors carrying molecular alterations of PIK3CA and/or PTEN.

[Single agent safety expansion arm]: Patients with histologically-confirmed, advanced unresectable solid tumors including CS patients who have progressed on (or not been able to tolerate) standard therapy within three months before screening visit or for whom no standard anticancer therapy exists. Patients will be prescreened for molecular alterations affecting PIK3CA and/or PTEN. Patients with NSCLC will also be pre-screened for EGFR mutation.

Exclusion Criteria:

Patients who have brain metastases, which are progressive and/or requiring medical intervention for symptom control
Prior treatment with a PI3K inhibitor
Acute or chronic liver disease or renal disease
Acute or chronic pancreatitis
Patients with unresolved diarrhea ≥ CTCAE grade 2
Impaired cardiac function or clinically significant cardiac diseases
Patients with diabetes mellitus requiring insulin treatment
Patients with known coagulopathies
Patients with a history of photosensitivity reactions to other drugs
Any of the following ophthalmological findings:
Progressive eye disease that could lead to severe loss of visual acuity or visual field
loss during the study period
Inability to perform the ophthalmic procedures required in this protocol
Other concurrent severe and/or uncontrolled concomitant medical conditions (e.g. active or uncontrolled infection) that could cause unacceptable safety risks or compromise compliance with the protocol.

Other protocol-defined inclusion/exclusion criteria may apply