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NCT01284192 · ClinicalTrials.gov registry record · Phase 1
Study of an Investigational Drug, ASP3026, in Patients With Advanced Malignancies (Solid Tumors and B-Cell Lymphoma)
A Phase 1 study of Solid Tumor and B-cell Lymphoma, sponsored by Astellas Pharma.
- Completed
- Registry status
- Phase 1
- Development phase
- 46
- Enrollment target
- 6
- Study locations
NCT01284192 is a Phase 1 study of Solid Tumor and B-cell Lymphoma that has completed, run by Astellas Pharma. The registered enrollment target is 46 participants, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (79% lower). The trial reports 6 study locations across 4 states.
The verdict
NCT01284192, a Phase 1 study of Solid Tumor and B-cell Lymphoma, has completed, sponsored by Astellas Pharma.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 46 participants
- Enrollment target
- 6
- Study locations
Study Summary
This study is to evaluate the safety and anti-tumor activity of ASP3026 in patients with advanced malignancies (solid tumors and B-cell lymphoma).
Conditions Studied
Interventions
- DRUG ASP3026
Study Locations (6)
California
- Site US160 - Orange
- Site US184 - Sacramento
Texas
- Site US2492 - Houston
- Site US1905 - San Antonio
Illinois
- Site US11 - Chicago
Michigan
- Site US2688 - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 46 participants |
| Start Date | 2010-12 |
| Est. Completion | 2016-03 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01284192
The ClinicalTrials.gov registry entry for NCT01284192 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 46 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 221-participant average among 196 other Solid Tumor trials with a reported enrollment target (79% lower). The listed sponsor is Astellas Pharma, which has 165 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which ASP3026 is the first listed.
NCT01284192 reports 6 study locations spanning 4 distinct geographic areas - top geographies include California, Texas, Illinois.
Frequently Asked Questions
What is clinical trial NCT01284192 about?
NCT01284192 is a clinical study titled "Study of an Investigational Drug, ASP3026, in Patients With Advanced Malignancies (Solid Tumors and B-Cell Lymphoma)". This study is to evaluate the safety and anti-tumor activity of ASP3026 in patients with advanced malignancies (solid tumors and B-cell lymphoma).
What is the current status of trial NCT01284192?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2010-12. Estimated completion is 2016-03.
What conditions does trial NCT01284192 study?
This clinical trial studies the following conditions: Solid Tumor, B-cell Lymphoma, Advanced Malignancies, Positive for Anaplastic Lymphoma Kinase, Positive for Proto-Oncogene Tyrosine-Protein Kinase ROS.
What interventions are being tested in trial NCT01284192?
The interventions under investigation include: ASP3026 (DRUG).
Who is sponsoring clinical trial NCT01284192?
This trial is sponsored by Astellas Pharma, which has 165 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01284192 being conducted?
This trial has 6 study locations across California, Illinois, Michigan, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.