Inclusion Criteria:

- Subjects, at least 18 years of age, with advanced or refractory solid tumors in whom
gemcitabine (Treatment A) or cisplatin plus gemcitabine (Treatment B) is appropriate
medical therapy as determined by the treating physician

- Histological or cytological documentation of non-hematologic, malignant solid tumor,
excluding primary brain or spinal tumors, with no current involvement in the CNS

- At least one measurable lesion or evaluable disease, as per RECIST 1.1

- Eastern Cooperative Oncology Group (ECOG) Performance Status Assessment of 0 or 1

- Life expectancy of at least 12 weeks

- Alanine aminotransferase (ALT) ≤ 3.0 x upper limit of normal (ULN; ≤5 x ULN for
subjects with liver involvement with cancer)

- Aspartate aminotransferase (AST) ≤ 3.0 x ULN (≤ 5 x ULN for subjects with liver
involvement with cancer)

- Total bilirubin ≤ 2.0 x ULN

- Serum creatinine ≤ 1.5 x ULN

- Prothrombin time-international normalized ratio/partial thromboplastin time
(PT-INR/PTT) < 1.5 x ULN (Subjects who are being therapeutically anticoagulated with
an agent such as coumadin or heparin will be allowed to participate provided that no
prior evidence of underlying abnormality in these parameters exists). Low-dose
aspirin is permitted (≤ 100 mg daily).

Exclusion Criteria:

- History of cardiac disease congestive; congestive heart failure > New York Heart
Association functional classification system (NYHA) Class II; active coronary artery
disease, myocardial infarction within 6 months prior to study entry; new onset angina
within 3 months prior to study entry or unstable angina, or ventricular cardiac
arrhythmias requiring anti-arrhythmic therapy

- Current diagnosis of Type 1 or 2 diabetes mellitus, hyperglycemia (defined as
consistent fasting blood glucose > 125 mg/dL) or HgBA1c ≥ 7%

- Use of systemic corticosteroids within 2 weeks of the start of study treatment
(topical or inhaled steroids are permitted). Single doses of systemic corticosteroids
given as premedication for procedures or non-study drugs may be administered up to 24
hours of first dosing of BAY 80-6946.

- Poorly controlled hypertension, defined as systolic blood pressure (BP) > 150 mmHg or
diastolic pressure > 90 mmHg, despite optimal medical management

- Poorly controlled seizure disorder

- Subjects undergoing renal dialysis

- Use of strong inhibitors of CYP3A4 (eg, ketoconazole, itraconazole, clarithromycin,
ritonavir, indinavir, nelfinavir, nefazodone and saquinavir) and strong inducers of
CYP3A4 (eg, rifampin) are not permitted from Day -14 of Cycle 1 and for the duration
of the study.

- Anticancer chemotherapy or immunotherapy during the study or within 4 weeks of first
study treatment

- Hormonal therapy during the study or within 2 weeks of first study treatment.

- Bisphosphonate therapy during the first 2 cycles of treatment

- Biological response modifiers, such as granulocyte colony stimulating factor (G-CSF)
within 4 weeks of first study treatment

- Radiotherapy to target lesions during study or within 4 weeks of first study
treatment

- Known hypersensitivity to the study drugs or active substances or excipients of the
preparations

- Use of St John's Wort is prohibited from Day -14 and for the duration of the study