Viewing Study NCT00277836



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Last Modification Date: 2024-10-26 @ 9:22 AM
Study NCT ID: NCT00277836
Status: TERMINATED
Last Update Posted: 2006-12-08
First Post: 2006-01-13

Brief Title: Study Evaluating MST-997 in Advanced Malignant Solid Tumors
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: A Phase 1 Dose-Escalation Study of Intravenous MST-997 Formulated in Polysorbate 80 Diluent Administered Weekly in Subjects With Advanced Malignant Solid Tumors
Status: TERMINATED
Status Verified Date: 2006-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: MST-997 is a taxane analog with the potential to treat subjects with a variety of tumor types Preclinical data demonstrated that MST-997 inhibited tumor growth when administered intravenously IV This phase 1 dose escalation study is designed to evaluate the safety and tolerability of if IV MST-997 formulated in Polysorbate 80 Diluent can be safely administered on a weekly basis
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None