Pralatrexate and Fluorouracil in Treating Patients With Recurrent Solid Tumors
Public ClinicalTrials.gov record NCT01206465. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase I Clinical Trial of Sequential Pralatrexate Followed by a 48-hour Infusion of 5- Fluorouracil Given Every Other Week in Adult Patients With Solid Tumors
Study identification
- NCT ID
- NCT01206465
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1
- Lead sponsor
- University of Nebraska
- Other
- Enrollment
- 29 participants
Conditions and interventions
Interventions
- DNA analysis Genetic
- fluorouracil Drug
- high performance liquid chromatography Other
- laboratory biomarker analysis Other
- nucleic acid sequencing Genetic
- pharmacogenomic studies Other
- pharmacological study Other
- polymerase chain reaction Genetic
- polymorphism analysis Genetic
- pralatrexate Drug
Genetic · Drug · Other
Eligibility (public fields only)
- Age range
- 19 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Sep 13, 2010
- Primary completion
- Feb 3, 2015
- Completion
- May 31, 2017
- Last update posted
- Dec 25, 2023
2010 – 2017
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Nebraska Medical Center, Eppley Cancer Center | Omaha | Nebraska | 68198-6805 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01206465, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Dec 25, 2023 · Synced May 16, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01206465 live on ClinicalTrials.gov.