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| Sponsor: | Wyeth is now a wholly owned subsidiary of Pfizer |
|---|---|
| Information provided by: | Wyeth is now a wholly owned subsidiary of Pfizer |
| ClinicalTrials.gov Identifier: | NCT00088647 |
Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Neoplasms |
Drug: MST-997 |
Phase I |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety Study Intervention Model: Factorial Assignment Masking: Open Label Primary Purpose: Treatment |
| 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 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, New York | |
| New York, New York, United States, 10016 | |
| United States, Ohio | |
| Cleveland, Ohio, United States, 44195 | |
| United States, Tennessee | |
| Nashville, Tennessee, United States, 37232 | |
| Study Director: | Medical Monitor, MD | Wyeth is now a wholly owned subsidiary of Pfizer |
More Information
| ClinicalTrials.gov Identifier: | NCT00088647 History of Changes |
| Other Study ID Numbers: | 3161K1-100 |
| Study First Received: | July 30, 2004 |
| Last Updated: | December 7, 2006 |
| Health Authority: | United States: Food and Drug Administration |
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advanced malignant solid tumors breast cancer |
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Neoplasms |