Clinical trial

Study of Pralatrexate & Gemcitabine With B12 & Folic Acid to Treat…

NCT00481871 · Acrotech Biopharma Inc., Industry · Completed

Key facts

NCT number NCT00481871
Title Study of Pralatrexate & Gemcitabine With B12 & Folic Acid to Treat Relapsed/Refractory Lymphoproliferative Malignancies
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
Lead sponsor Acrotech Biopharma Inc., Industry
Status Completed
Phase Phase 1/Phase 2
Study type Interventional
Conditions Relapsed or Refractory Lymphoproliferative Malignancies, Hodgkin's Lymphoma, Peripheral T-cell Lymphoma, B-cell Lymphoma, Waldenstrom's Macroglobulinemia
Intervention type Dietary Supplement, Drug
Interventions Pralatrexate Injection, Gemcitabine Hydrochloride, Vitamin B12, Folic Acid
Enrollment 119
Start date May 1, 2007
Primary completion May 1, 2011
Completion Aug 1, 2011
First posted Jun 4, 2007
Last update posted Jan 7, 2020
Countries United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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