A Study to Evaluate the Potential Benefit of the Addition of BYL719 to Paclitaxel in the Treatment of Breast Cancer and Head-and-neck Cancer

Inclusion criteria For entire trial:

- Adult > or = 18 years old
- has signed the Informed Consent Form (ICF)
- has at least one measurable or non-measurable disease as per RECIST 1.1
- has tumor tissue available for the analysis as described in the protocol
- has adequate bone marrow and organ function as defined in the protocol
- is able to swallow and retain oral medication for the dose escalation part, ALL above PLUS
- has a histologically-confirmed, advanced unresectable solid tumors who have progressed on standard therapy (or not been able to tolerate) within three months before screening/baseline visit or for whom no standard anticancer therapy exists.

- has an Eastern Cooperative Oncology Group (ECOG) performance status ≤2 For dose expansion part, patient has ALL of above first six criteria PLUS either: 9- has a histologically/cytologically-confirmed HNSCC as detailed in the protocol and an ECOG performance status ≤ 1 or:

Patient is a Female with a histologically and/or cytologically confirmed diagnosis of breast cancer as detailed in the protocol and an ECOG performance status ≤ 1

Common exclusion criteria to Dose escalation and Dose expansion parts:

- has received previous treatment with a PI3K or AKT inhibitor as described in the protocol
- has a known hypersensitivity to paclitaxel or other products containing Cremophor
- has a contraindication to use the standard pre-treatment for paclitaxel
- has a primary central nervous system (CNS) tumor or CNS tumor involvement as detailed in the protocol
- has not recovered to grade 1 or better (except alopecia) from related side effects of any prior antineoplastic therapy
- has received radiotherapy > or = 4 weeks prior to starting study drugs, with exception of palliative radiotherapy, who has not recovered from side effects of such therapy to baseline or Grade ≤ 1 and/or from whom ≥ 30% of the bone marrow was irradiated
- has peripheral sensory neuropathy with functional impairment (CTC grade 2 neuropathy or higher)
- has undergone major surgery ≤ 4 weeks prior to starting study treatment or who has not recovered from side effects of such procedure
- has a clinically significant cardiac disease or impaired cardiac function as detailed in the protocol
- is currently receiving medication with a known risk of prolonging the QT interval or inducing Torsades de Pointes (TdP) and the treatment cannot either be discontinued or switched to a different medication prior to starting study drug treatment
- has diabetes mellitus requiring insulin treatment and/or with clinical signs
- has impaired gastrointestinal (GI) function or GI disease as described in the protocol
- has a known positive serology for human immunodeficiency virus (HIV), active Hepatitis B, and/or active Hepatitis C infection
- has any other condition that would, in the Investigator's judgment, preclude patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures
- is currently receiving treatment with drugs known to be moderate or strong inhibitors or inducers of isoenzymes CYP3A or CYP2C8 as detailed in the protocol
- is currently receiving treatment with agents that are metabolized solely by CYP3A and/or have a narrow therapeutic window
- has a history of another malignancy within 2 years prior to starting study treatment, except cured basal cell carcinoma of the skin or excised carcinoma in situ of the cervix
- Patient has a history of non-compliance to medical regimen or inability to grant consent
- Pregnant or nursing (lactating) women
- does not apply highly effective contraception during the study and through the duration as defined in the protocol

For the HNSCC patient's cohort additional exclusion criteria are:

21- Treatment with more than one prior chemotherapy for recurrent/metastatic disease as detailed in the protocol 22- Prior taxane treatment for metastatic disease additional exclusion criteria for breast cancer patients' cohort:

- has received any prior cytotoxic therapy for the inoperable locally advanced (recurrent or progressive) or metastatic disease, or who had a progression/recurrent disease within 6 months after completion of an adjuvant/neoadjuvant therapy as described in the protocol

Other protocol-defined inclusion/exclusion criteria may apply