Leucovorin

Generic Name
Leucovorin
Brand Names
EnBrace HR, EnLyte, Lederle Leucovorin
Drug Type
Small Molecule
Chemical Formula
C20H23N7O7
CAS Number
58-05-9
Unique Ingredient Identifier
Q573I9DVLP
Background

Folinic Acid (also known as 5-formyl tetrahydrofolic acid or leucovorin) is the 5-formyl derivative of tetrahydrofolic acid, a necessary co-factor in the body. Commercially available leucovorin is composed of a 1:1 racemic mixture of the dextrorotary and levorotary isomers, while levoleucovorin contains only the pharmacologically active levo-isomer. In vitro...

Indication

For the treatment of osteosarcoma (after high dose methotrexate therapy). Used to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists, and to treat megaloblastic anemias due to folic acid deficiency. Also used in combination with 5-fluorouracil to prolong survival in t...

Associated Conditions
Advanced Colorectal Cancer, Advanced Esophageal Cancers, Anemia of Pregnancy, Bladder Cancer, Folate and iron deficiency, Folate deficiency, Folic acid antagonist overdose, Iron Deficiency (ID), Macrocytic anemia, Megaloblastic anemia, Pancreatic Metastatic Cancer, Postpartum Anemia, Stage IV Gastric Cancer, Hypochromic anemia, Methotrexate toxicity, Normochromic anemia, Pyrimethamine hematologic toxicity
Associated Therapies
-

A Phase I Trial of 5-Fluorouracil Given With 776C85 (GW776) and Low-Dose Leucovorin in Adult Patients With Solid Tumors

Phase 1
Completed
Conditions
First Posted Date
2002-12-10
Last Posted Date
2006-07-17
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
50
Registration Number
NCT00001579
Locations
🇺🇸

National Cancer Institute (NCI), Bethesda, Maryland, United States

A Phase I Study of Weekly Gemcitabine in Combination With Infusional Fluorodeoxyuridine and Oral Calcium Leucovorin in Adult Cancer Patients

Phase 1
Completed
Conditions
First Posted Date
2002-12-10
Last Posted Date
2008-03-04
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
60
Registration Number
NCT00001449
Locations
🇺🇸

National Cancer Institute (NCI), Bethesda, Maryland, United States

A Pilot Trial of Sequential Chemotherapy With Antimetabolite Induction, High-Dose Alkylating Agent Consolidation With Peripheral Blood Progenitor Cell Support, and Intensification With Paclitaxel and Doxorubicin for Patients With High-Risk Breast Cancer

Phase 2
Completed
Conditions
First Posted Date
2002-12-10
Last Posted Date
2008-03-04
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
55
Registration Number
NCT00001498
Locations
🇺🇸

National Cancer Institute (NCI), Bethesda, Maryland, United States

Phase I Study of PN401, Fluorouracil, Leucovorin and CPT-11 in Patients With Solid Tumors

Phase 1
Terminated
Conditions
First Posted Date
2002-09-06
Last Posted Date
2005-06-24
Lead Sponsor
Wellstat Therapeutics
Target Recruit Count
24
Registration Number
NCT00044785
Locations
🇺🇸

University of Maryland, Greenebaum Cancer Center, Baltimore, Maryland, United States

A Trial of an Investigational Drug for the Prevention of Diarrhea Associated With Irinotecan/5FU/Leucovorin Chemotherapy in Previously Untreated Metastatic Colorectal Cancer

Phase 2
Terminated
Conditions
First Posted Date
2002-06-27
Last Posted Date
2016-12-01
Lead Sponsor
Celgene Corporation
Registration Number
NCT00040391
Locations
🇺🇸

Research Center, Milwaukee, Wisconsin, United States

For Prevention of Diarrhea in Patients Diagnosed With Metastatic Colorectal Cancer Treated With Chemotherapy

Phase 2
Terminated
Conditions
First Posted Date
2002-05-17
Last Posted Date
2008-09-29
Lead Sponsor
Pfizer
Target Recruit Count
212
Registration Number
NCT00037180
Locations
🇺🇸

Pfizer Investigational Site, Milwaukee, Wisconsin, United States

Leucovorin for the Treatment of 5 q Minus Syndrome

First Posted Date
2000-03-23
Last Posted Date
2008-03-04
Lead Sponsor
National Institutes of Health Clinical Center (CC)
Target Recruit Count
14
Registration Number
NCT00004997
Locations
🇺🇸

Warren G. Magnuson Clinical Center (CC), Bethesda, Maryland, United States

A Phase I Study of Isolated Hepatic Perfusion With Escalating Dose Melphalan Followed by Postoperative Hepatic Arterial Floxuridine and Leucovorin for Metastatic Unresectable Colorectal Cancers of the Liver

First Posted Date
1999-11-04
Last Posted Date
2008-03-04
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
28
Registration Number
NCT00001576
Locations
🇺🇸

National Cancer Institute (NCI), Bethesda, Maryland, United States

© Copyright 2024. All Rights Reserved by MedPath