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Brief Title: Phase I, Open-label, Dose-escalation, Safety and PK Study of AZD6918
Official Title: A Phase I, Open-Label, Dose-Escalation Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD6918 Administered Daily as a Single Agent and in Combination Treatment in Adult Patients With Refractory Solid Malignancies
Study ID: NCT00733031
Brief Summary: The primary purpose of this study is to find out what the maximum tolerated dose is for an experimental drug called AZD6918 based on the side effects experienced by patients with advanced solid malignancies that receive daily AZD6918 alone. It is possible that AZD6918 will be administered twice daily. Then maximum tolerated doses in combination with either gemcitabine or pemetrexed will also be investigated.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Aurora, Colorado, United States
Research Site, Nashville, Tennessee, United States
Name: Judith Ochs, MD
Affiliation: AstraZeneca
Role: STUDY_DIRECTOR
Name: Jeffrey Infante, MD
Affiliation: SCRI Development Innovations, LLC
Role: PRINCIPAL_INVESTIGATOR
Name: Lia Gore, MD
Affiliation: University of Colorado, Denver
Role: PRINCIPAL_INVESTIGATOR