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Study to Evaluate Efficacy of CO-1.01 as Second Line Therapy for Gemcitabine-Refractory Stage IV Pancreatic Adenocarcinoma
NCT01233375 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine whether CO-1.01 is safe and effective for treating metastatic pancreatic cancer that did not respond to gemcitabine.
Conditions Studied
Interventions
- DRUG CO-1.01
Study Locations (13)
Florida
- Palm Beach Institute / Collaborative Research Group — Boynton Beach
- University of Miami — Miami
New York
- Memorial Sloan-Kettering Cancer Center — New York
- Columbia University Medical Center, Milstein Hospital — New York
Arizona
- Arizona Cancer Center at University of Arizona — Tucson
Colorado
- Rocky Mountain Cancer Center — Denver
Georgia
- Piedmont Healthcare Research Institute (PHRI) — Atlanta
Kentucky
- Norton Cancer Institute Research Program — Louisville
Maryland
- Johns Hopkins Oncology Center — Baltimore
Massachusetts
- Massachusetts General Hospital (MGH) — Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2011-04 |
| Est. Completion | 2013-03 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01233375
The ClinicalTrials.gov registry entry for NCT01233375 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 19 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clovis Oncology, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Metastatic Pancreatic Adenocarcinoma appearing as the primary indexed condition, and to 1 intervention — of which CO-1.01 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01233375 reports 13 study locations spanning 11 distinct geographic areas — top geographies include Florida, New York, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01233375 about?
NCT01233375 is a clinical study titled "Study to Evaluate Efficacy of CO-1.01 as Second Line Therapy for Gemcitabine-Refractory Stage IV Pancreatic Adenocarcinoma". The purpose of this study is to determine whether CO-1.01 is safe and effective for treating metastatic pancreatic cancer that did not respond to gemcitabine.
What is the current status of trial NCT01233375?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 19 participants. The study started on 2011-04. Estimated completion is 2013-03.
What conditions does trial NCT01233375 study?
This clinical trial studies the following conditions: Metastatic Pancreatic Adenocarcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01233375?
The interventions under investigation include: CO-1.01 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01233375?
This trial is sponsored by Clovis Oncology, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01233375 being conducted?
This trial has 13 study locations across Arizona, Colorado, Florida, Georgia, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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