A Study to Look at How a Single Oral Dose of 14C-OSI-906 is Absorbed, Broken Down and Eliminated in the Body

This study includes two parts: Part A

Subjects will be admitted to the clinical research unit on Day -1 and remain confined to the
unit until post dosing discharge criteria are met up to a maximum of 10 days. On Day 1,
subjects will receive a single oral dose of 14C-labeled OSI-906.

Part B (optional)

Once the subject has completed part A, the subject may elect to continue participation in
Part B. Subjects will receive OSI-906 (non-radiolabeled) twice daily by mouth. Subjects will
be seen for scheduled visits every 7 days for the first 36 days and then every 21 days.

Inclusion Criteria:

- The subject has histologically or cytologically confirmed diagnosis of advanced solid
tumor (measurable or non-measurable disease) for which no conventional therapy is
available

- The subject has an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) ≤
2

- The subject has a predicted life expectancy ≥12 weeks

- The subject has a fasting glucose ≤125 mg/dL (7 mmol/L) at Screening, Day -1 and
pre-dose Day 1

- The subject has adequate organ function defined by the following laboratory
parameters:

- absolute neutrophil count (ANC) ≥1.5 x 10 9/L

- platelet count ≥100 x 10 9/L

- total bilirubin ≤1.5 x upper limit of normal (ULN)

- aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN,
or ≤ 5 x ULN if subject has documented liver metastases

- serum creatinine ≤1.5 x ULN

- potassium, calcium, and magnesium within normal limits or determined by the
investigator to be not clinically significant (NCS)

- The subject has a negative cotinine test

- If male, is surgically sterile, or is using a medically acceptable method to prevent
pregnancy and agrees to continue using this method while participating in the study
and for 90 days after the last dose of study medication

- If female, the subject is surgically sterile or status post hysterectomy,
post-menopausal, or is using 2 forms of medically acceptable methods of birth control,
one of which must be a barrier method to prevent pregnancy and agrees to continue
using this method from screening until 90 days after the last dose of study medication

- If female, the subject must not be breastfeeding at Screening, during the study period
and for 90 days after last dose of study drug administration

- If female, the subject must not donate ova starting at Screening, and throughout the
study period and for 90 days after last dose of study drug administration

- Female subject of child bearing potential has a negative pregnancy test at Screening
and Day -1

Exclusion Criteria:

- The subject has Type 1 or Type 2 diabetes mellitus currently requiring insulinotropic
or insulin therapy

- The subject has a history of poorly controlled gastrointestinal disorder (s) that
could affect the absorption or metabolism of study drug

- The subject has used IGF-1R inhibitor therapy in last 6 months

- The subject has hepatocellular carcinoma

- The subject has used a CYP1A2 inhibitor or inducer within 14 days prior to Day 1

- The subject has used drugs with a risk of causing QTc interval prolongation and
Torsade de Pointes (TdP) within 14 days prior to Day 1

- The subject has a history (within last 6 months) of significant cardio-vascular
disease

- The subject has a history (within the last 6 months) of significant arrhythmia
disease, unless the disease is well-controlled with medication per the Principal
Investigator's clinical judgment

- The subject has had major surgery ≤ 3 weeks prior to Day 1

- The subject has had radiation ≤ 3 weeks prior to Day 1

- The subject has had chemotherapy ≤ 3 weeks prior to Day 1

- The subject has participated in a radiolabeled study in the last 12 months

- The subject has a history of cerebrovascular accident (CVA) within 6 months prior to
Day 1 or that resulted in ongoing neurologic instability

- The subject has an active infection or serious underlying medical condition (including
any type of active seizure disorder within 12 months prior to Day 1) that would impair
the ability of the subject to receive study drug

- The subject has participated in any interventional clinical study within 21 days or
has been treated with any investigational drugs within 30 days or 5 half lives
whichever is longer, prior to the initiation of Screening

- The subject has a history of any psychiatric condition that might impair the subject's
ability to understand or to comply with the requirements of the study or to provide
informed consent

- The subject is pregnant or lactating

- The subject has symptomatic brain metastases that are not stable, require steroids, or
that have required radiation and/or other related treatment, (i.e., anti-epileptic
medication) within 28 days prior to Day 1

- The subject has a history of allergic reactions attributed to compounds of similar
chemical or biologic composition to the study drug