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

NCT01336933 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2023-09-22

Study results available
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Summary

This phase II trial studies how well combination chemotherapy and pralatrexate works in treating patients with non-Hodgkin lymphoma (NHL). Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing

Conditions

  • Anaplastic Large Cell Lymphoma
  • Angioimmunoblastic T-cell Lymphoma
  • Hepatosplenic T-cell Lymphoma
  • Peripheral T-cell Lymphoma

Interventions

DRUG

prednisone

Given PO

DRUG

cyclophosphamide

Given IV

DRUG

etoposide

Given PO or IV

DRUG

Vincristine

Given IV

DRUG

pralatrexate

Given IV

OTHER

laboratory biomarker analysis

Correlative studies

GENETIC

comparative genomic hybridization

Correlative studies

GENETIC

gene expression analysis

Correlative studies

GENETIC

nucleic acid sequencing

Correlative studies

GENETIC

mutation analysis

Correlative studies

OTHER

immunohistochemistry staining method

Correlative studies

GENETIC

microarray analysis

Correlative studies

GENETIC

RNA analysis

Correlative studies

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Spectrum Pharmaceuticals, Inc

    collaborator INDUSTRY
  • University of Nebraska

    lead OTHER

Principal Investigators

  • Julie M Vose · University of Nebraska

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-06
Primary Completion
2016-12-28
Completion
2016-12-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01336933 on ClinicalTrials.gov