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Completed Phase 1Phase 2 Interventional Results available

Study of Pralatrexate & Gemcitabine With B12 & Folic Acid to Treat Relapsed/Refractory Lymphoproliferative Malignancies

ClinicalTrials.gov ID: NCT00481871

Public ClinicalTrials.gov record NCT00481871. 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 Oct 21, 2026, 6:51 PM 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 1/2a Open-label Study of Pralatrexate and Gemcitabine With Vitamin B12 and Folic Acid Supplementation in Patients With Relapsed or Refractory Lymphoproliferative Malignancies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is for patients with lymphoproliferative malignancies that have progressed after receiving a previous treatment (relapsed) or are no longer responding to treatment (refractory). To be in this study, patients must have certain types of Hodgkin's lymphoma (HL), peripheral T-cell lymphoma (PTCL), or B-cell lymphoma, including Waldenstrom's macroglobulinemia. This study is being done to find doses of the combination of pralatrexate and gemcitabine with vitamin B12 and folic acid that can be safely given to patients with these types of lymphoma and explore the effectiveness of the treatment.

Study identification

NCT ID
NCT00481871
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Acrotech Biopharma Inc.
Industry
Enrollment
119 participants

Conditions and interventions

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
May 2007 (Type not available)
Primary completion
May 2011 (Actual)
Completion
Aug 2011 (Actual)
Last update posted
Jan 7, 2020

2007 – 2011

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
University of California at Los Angeles Los Angeles California 90095-7077 —
Stanford University School of Medicine Stanford California 94305 —
Rocky Mountain Cancer Center Denver Colorado 80218 —
University of Chicago Hospital Chicago Illinois 60637 —
Dana-Farber Cancer Institute Boston Massachusetts 02115-6013 —
Washington University School of Medicine St Louis Missouri 63110 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
The Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601 —
New York University Hospital New York New York 10016 —
Memorial Sloan-Kettering Cancer Center New York New York 10017 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Medical University of South Carolina Charleston South Carolina 29425 —
UT MD Anderson Cancer Center Houston Texas 77030 —
Cancer Therapy & Research Center San Antonio Texas 78229-4427 —
Fred Hutchinson Cancer Research Center Seattle Washington 98109 —

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 NCT00481871, 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 Jan 7, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00481871 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →