Ignite Creation Date:
2024-05-05 @ 11:35 AM
Last Modification Date:
2024-10-26 @ 9:10 AM
Study NCT ID:
NCT00088647
Status:
TERMINATED
Last Update Posted:
2006-12-08
First Post:
2004-07-30
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 Intralipid 20 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:
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:
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