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NCT00019656 · ClinicalTrials.gov registry record · Phase 1
Perifosine in Treating Patients With Refractory Solid Tumors or Hematologic Cancer
A Phase 1 study of Lymphoma and Leukemia, sponsored by National Cancer Institute (NCI).
- Completed
- Registry status
- Phase 1
- Development phase
- 2
- Study locations
NCT00019656: Completed Phase 1 study of Lymphoma and Leukemia, sponsored by National Cancer Institute (NCI).
NCT00019656 is a Phase 1 study of Lymphoma and Leukemia that has completed, run by National Cancer Institute (NCI). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00019656, a Phase 1 study of Lymphoma and Leukemia, has completed, sponsored by National Cancer Institute (NCI).
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 2
- Study locations
Study Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I trial to study the effectiveness of perifosine in treating patients who have refractory solid tumors or hematologic cancer.
Conditions Studied
Interventions
- DRUG perifosine
Study Locations (2)
Maryland
- Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support - Bethesda
- NCI - Center for Cancer Research - Bethesda
Trial Details
| Field | Value |
|---|---|
| Start Date | 1999-08 |
| Phase | Phase 1 |
What the finished NCT00019656 record still lists
NCT00019656 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.
The record links to 5 conditions, with Lymphoma appearing as the primary indexed condition, and to 1 intervention - of which perifosine is the first listed.
NCT00019656 reports a single indexed study location in Maryland.
Frequently Asked Questions
What is clinical trial NCT00019656 about?
NCT00019656 is a clinical study titled "Perifosine in Treating Patients With Refractory Solid Tumors or Hematologic Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I trial to study the effectiveness of perifosine in treating patients who have refractory solid tumors or hematologic cancer.
What is the current status of trial NCT00019656?
This trial is currently completed. It is a Phase 1 study. The study started on 1999-08.
What conditions does trial NCT00019656 study?
This clinical trial studies the following conditions: Lymphoma, Leukemia, Myelodysplastic Syndromes, Unspecified Adult Solid Tumor, Protocol Specific, Myelodysplastic/Myeloproliferative Neoplasms.
What interventions are being tested in trial NCT00019656?
The interventions under investigation include: perifosine (DRUG).
Who is sponsoring clinical trial NCT00019656?
This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00019656 being conducted?
This trial has 2 study locations across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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