NIPH Clinical Trials Search

Basic Information

Recruitment status
Health condition(s) or Problem(s) studied	solid tumor, gastric cancer
Date of first enrollment	02/09/2011
Target sample size	33
Countries of recruitment
Study type	Interventional
Intervention(s)	investigational material(s) Generic name etc : E7050 INN of investigational material : Therapeutic category code : 424 Antineoplastic preparations extracted from plants Dosage and Administration for Investigational material : oral

Outcome(s)

Primary Outcome	Investigation of tolerability and safety of E7050 administered continuously once daily for 4 weeks to subjects with solid tumor and gastric cancer.
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum	>= 20age old
Age maximum	<= 74age old
Gender	Both
Include criteria	1. Aged from 20 to less than 75 years old at the time of obtaining informed consent. 2. Histological or cytological diagnosis of solid tumors. 3. Subjects who have progressed after treatment with approved therapies or for whom there are no standard effective therapies available. 4. Adequate organ function. 5. Subjects who have no carryover of effect from prior therapy or no adverse drug reactions (excluding alopecia) that may affect the safety evaluation of the investigational drug. 6. Performance Status (PS) 0-1 established by Eastern Cooperative Oncology Group (ECOG). 7. Expected to survive for 3 months or longer after starting administration of the investigational drug.
Exclude criteria	1. Females who are pregnant or breast feeding. 2. Brain metastases with clinical symptoms or which requires treatment. 3. Serious complications or disease history. 4. Subjects who cannot take oral medication. 5. Using antiplatelet/anticoagulant drugs. 6. Continuous using of drugs or foods that strongly inhibit or induce CYP3A4/5 or CYP2D6 during the study period. 7. Scheduled for surgery during the study period. 8. Known to be HIV, HBV or HCV positive. 9. Suffering from psychotic disorder(s) and/or unstable recurrent affective disorder(s) evident by use of anti-psychotics or have had a suicide attempt(s) within approximately the last 2 years. 10. History of drug or alcohol dependency or abuse within 2 years. 11. Presence of a progressive central nervous system (CNS) disease, including degenerative CNS diseases and progressive tumors. 12. Received any other investigational product or device within 4 weeks before administration.