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Brief Title: A Study of ZSTK474 in Japanese Patients With Advanced Solid Malignancies
Official Title: A Phase 1, Multi-Center, Open Label, Uncontrolled, Serial Cohort, Dose Escalation Study of the Safety, Tolerability, Pharmacokinetics and Efficacy of ZSTK474 in Japanese Patients With Advanced Solid Malignancies
Study ID: NCT01682473
Brief Summary: To evaluate the safety (adverse events and dose-limiting toxicity) of daily oral doses of ZSTK474 in patients with advanced solid malignancies.
Detailed Description: Open-label, uncontrolled, serial cohort, dose-escalation study evaluating two different dosing regimens (Arm 1: cycles of 5 days on drug and 2 days off drug), Arm 2: cycles of 21 days on drug and 7 days off drug).
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
National Cancer Center Hospital East, Kashiwa-city, Chiba, Japan
The Cancer Institute Hospital of JFCR, Koto-ku, Tokyo, Japan
Name: Toshihiko Doi, MD, PhD
Affiliation: National Cancer Center Hospital East
Role: PRINCIPAL_INVESTIGATOR
Name: Shunji Takahashi, MD
Affiliation: The Cancer Institute Hospital of JFCR
Role: PRINCIPAL_INVESTIGATOR