ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Combination Chemotherapy and Pralatrexate as First-Line Therapy in Treating Patients With Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT01336933

Public ClinicalTrials.gov record NCT01336933. 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.

ClinicalTrials.gov public records Last synced May 18, 2026, 4:10 AM EDT

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 II Study of Cyclophosphamide, Etoposide, Vincristine and Prednisone (CEOP) Alternating With Pralatrexate (P) as Front Line Therapy for Patients With Stage II, III and IV Peripheral T-Cell Non-Hodgkin Lymphoma

Study identification

NCT ID
NCT01336933
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
University of Nebraska
Other
Enrollment
34 participants

Conditions and interventions

Interventions

  • RNA analysis Genetic
  • Vincristine Drug
  • comparative genomic hybridization Genetic
  • cyclophosphamide Drug
  • etoposide Drug
  • gene expression analysis Genetic
  • immunohistochemistry staining method Other
  • laboratory biomarker analysis Other
  • microarray analysis Genetic
  • mutation analysis Genetic
  • nucleic acid sequencing Genetic
  • pralatrexate Drug
  • prednisone Drug

Genetic · Drug · Other

Eligibility (public fields only)

Age range
18 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
Jul 5, 2011
Primary completion
Dec 27, 2016
Completion
Dec 27, 2016
Last update posted
Sep 21, 2023

2011 – 2016

United States locations

U.S. sites
9
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
Mayo Clinic, Arizona Scottsdale Arizona 85259
Stanford University Stanford California 94305
Emory University School Of Medicine Atlanta Georgia 30308
University of Chicago Chicago Illinois 60637
University of Massachusetts Medical School Worcester Massachusetts 01655
Mayo Clinic Rochester Minnesota 55905
Siteman Cancer Center, Washington University St Louis Missouri 63110
Eppley Cancer Center, University of Nebraska Medical Center Omaha Nebraska 68198-6805
Duke University Medical Center Durham North Carolina 27710

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 NCT01336933, 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 Sep 21, 2023 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01336933 live on ClinicalTrials.gov.

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