Spots Global Cancer Trial Database for Study Evaluating TTI-237 in Advanced Malignant Solid Tumors
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Trial Identification
Brief Title: Study Evaluating TTI-237 in Advanced Malignant Solid Tumors
Official Title: A Phase 1 Dose Escalation Study of TTI-237 Administered Intravenously Every 3 Weeks in Subjects With Advanced Malignant Solid Tumors
Study ID: NCT00195247
Conditions
Interventions
Study Description
Brief Summary: The purpose of this study is to evaluate the safety, tolerability, and maximum tolerated dose (MTD) of TTI-237 for the treatment of subjects with advanced malignant solid tumors.
Detailed Description:
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
, Scottsdale, Arizona, United States
, Los Angeles, California, United States
, Baltimore, Maryland, United States
Contact Details
Name: Medical Monitor
Affiliation: Wyeth is now a wholly owned subsidiary of Pfizer
Role: STUDY_DIRECTOR
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