Clinical trial
Study Evaluating Intravenous CMD-193 in Subjects With Advanced Malignant Solid…
NCT00257881 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Terminated
Key facts
| NCT number | NCT00257881 |
|---|---|
| Title | Study Evaluating Intravenous CMD-193 in Subjects With Advanced Malignant Solid Tumors |
| Official title | Phase 1 Dose-Escalation Study of Intravenous CMD-193 in Subjects With Advanced Malignant Solid Tumors |
| Lead sponsor | Wyeth is now a wholly owned subsidiary of Pfizer, Industry |
| Status | Terminated |
| Phase | Phase 1 |
| Study type | Interventional |
| Conditions | Neoplasms |
| Intervention type | Drug |
| Interventions | CMD-193 |
| Enrollment | 46 |
| Start date | Nov 1, 2005 |
| Completion | Dec 1, 2006 |
| First posted | Nov 23, 2005 |
| Last update posted | Dec 10, 2007 |
| Countries | Japan |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: