Study of LY2157299 in Japanese Participants With Cancer

Inclusion Criteria

• •Have histological or cytological evidence of a diagnosis of cancer that is advanced and/or metastatic. The participants must be, in the judgment of the investigator, an appropriate candidate for experimental therapy after available standard therapies have failed to provide clinical benefit for their disease.
• •Have the presence of measurable or nonmeasurable disease as defined by the Response Evaluation Criteria in Solid Tumors.
• •Have a performance status of higher than or equal to 1 on the Eastern Cooperative Oncology Group scale.
• •Have adequate hematologic, hepatic and renal function.
• •Have discontinued treatments for cancer excluding palliative treatments and recovered from the acute effects of therapy.
• •Have discontinued treatment at least 28 days prior to the enrollment for an experimental agent that has not received regulatory approval for any indication.
• •Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures.
• •Able to swallow tablets.
• •Have an estimated life expectancy, in the judgment of the investigator, that will permit the participant to complete greater than or equal to 2 cycles of treatment.
• •Males and females with reproductive potential: Must agree to use medically approved contraceptive precautions during the study and for 4 months following the last dose of study drug.
• •Females with child bearing potential: Have had a negative urine/serum pregnancy test greater than or equal to 7 days before the first dose of study drug and must also not be breastfeeding. If female who stops breastfeeding enters the study, the female must stop breastfeeding from the day of the first study drug administration until at least 30 days after the last administration.