Spots Global Cancer Trial Database for Study Evaluating MST-997 in Advanced Malignant Solid Tumors
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Trial Identification
Brief Title: Study Evaluating MST-997 in Advanced Malignant Solid Tumors
Official Title: A Phase 1 Dose-Escalation Study of Intravenous MST-997 Formulated in Intralipid 20% Administered Weekly in Subjects With Advanced Malignant Solid Tumors
Study ID: NCT00088647
Conditions
Interventions
Study Description
Brief Summary: The primary objective of this clinical research study is to evaluate the safety, tolerability, and maximum tolerated dose (MTD) of intravenous (IV) MST-997 formulated in Intralipid 20% administered on a weekly schedule to subjects with advanced malignant solid tumors.
Detailed Description:
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
, New York, New York, United States
, Cleveland, Ohio, United States
, Nashville, Tennessee, United States
Contact Details
Name: Medical Monitor, MD
Affiliation: Wyeth is now a wholly owned subsidiary of Pfizer
Role: STUDY_DIRECTOR
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