A Phase I Safety, Pharmacokinetic and Pharmacodynamic Study of PF-04217903 in Patients with Advanced Cancer

NOT ENROLLING
Protocol # :
08-157
Conditions
Neoplasms
Phase
I
Disease Sites
Lip, Oral Cavity and Pharynx
Esophagus
Stomach
Small Intestine
Colon
Rectum
Anus
Liver
Pancreas
Other Digestive Organ
Larynx
Lung
Other Respiratory and Intrathoracic Organs
Bones and Joints
Soft Tissue
Mycosis Fungoides
Other Skin
Breast
Cervix
Corpus Uteri
Ovary
Other Female Genital
Prostate
Other Male Genital
Urinary Bladder
Kidney
Other Urinary
Eye and Orbit
Brain and Nervous System
Thyroid
Unknown Sites
Ill-Defined Sites
Other Endocrine System
Kaposi's Sarcoma
Melanoma, Skin
Principal Investigator
Clark, Jeffrey, W

Trial Description

PF-04217903 may work in cancer by blocking the cell growth, migration and invasion of
tumor cells. PF-04217903 is a new member in a class of drugs called c-Met/hepatocyte
growth factor receptor tyrosine kinase inhibitors. This research study is the first time
PF-04217903 will be given to patients. PF-04217903 is taken by mouth daily.

Eligibility Requirements

Inclusion Criteria:

- Advanced solid tumors, histologically proven at diagnosis which is refractory to
standard of care or for whom no standard of care therapy is available

- Adequate blood cell counts, normal kidney function, and performance status of 0 or 1

Exclusion Criteria:

- Major surgery, radiation therapy or anti-cancer therapy within 2 weeks of starting
study treatment

- Prior stem cell transplant

- Active or unstable cardiac disease or heart attack within 12 months of starting
study treatment

08-157