Inclusion Criteria:

   - Histologic documentation of incurable, locally advanced, or metastatic solid
   malignancy that has failed to respond to at least one prior regimen or for which there
   is no standard therapy

   - Documented negative serum pregnancy test for women of childbearing potential and use
   of two forms of contraception. Contraception must be used while the patient is
   enrolled in the study and for 12 months after the patient discontinues from the study.

   - For men with female partners of childbearing potential, agreement to use a latex
   condom and to advise their female partner to use an additional method of contraception
   during the study and for 3 months after their last dose of GDC-0449.

   - Agreement not to donate blood or blood products during the study and for at least 12
   months after their last dose of GDC-0449

   - For male patients, agreement not to donate sperm during the study and for at least 3
   months after their last dose of GDC-0449

   - Adequate hematopoietic capacity

   - Adequate renal function

   - Adequate hepatic function

   - At least 3 weeks since the patient's last chemotherapy, investigational agent,
   radiation therapy, or major surgical procedure and recovery to pre-treatment baseline
   or stabilization of all treatment-related toxicities

Exclusion Criteria:

   - Active infection requiring intravenous (IV) antibiotics

   - Clinically important history of liver disease significantly impairing hepatic
   function, including active viral or other hepatitis, current alcohol abuse, or
   cirrhosis

   - Any medical condition or diagnosis that would likely impair absorption of an orally
   administered drug

   - Pregnant or lactating

   - Treatment with excluded medications, including strong CYP450 inhibitors and inducers,
   within 2 weeks of study entry

   - Male patients already receiving rosiglitazone

   - Male patients with a known contraindication to rosiglitazone

   - Female patients already receiving oral contraception < 14 days prior to Day 1

   - Female patients with known contraindication to oral contraceptions