US2017119715A1PendingUtilityA1

Therapeutic methods employing nitric oxide precursors

Assignee: UNIV VANDERBILTPriority: Feb 24, 2004Filed: Nov 4, 2016Published: May 4, 2017
Est. expiryFeb 24, 2024(expired)· nominal 20-yr term from priority
A61P 9/00A61P 37/06A61P 37/00A61P 9/12A61P 43/00A61P 31/04A61P 29/00A61K 31/198A61K 31/195A61P 1/04A01K 2217/05A61P 11/06C12N 9/93A61K 38/00A61P 11/00A61P 1/16A61P 15/10
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Claims

Abstract

Isolated polynucleotide molecules and peptides encoded by these molecules are used in the analysis of human carbamyl phosphate synthetase I phenotypes, as well as in diagnostic and therapeutic applications, relating to a human carbamyl phosphate synthetase I polymorphism. By analyzing genomic DNA or amplified genomic DNA, or amplified cDNA derived from mRNA, it is possible to type a human carbamyl phosphate synthetase I with regard to the human carbamyl phosphate synthetase I polymorphism, for example, in the context of diagnosing and treating hepatic veno-occlusive disease (HVOD) associated with bone marrow transplants.

Claims

exact text as granted — not AI-modified
1 - 10 . (canceled) 
     
     
         11 . A method of treating or preventing bone marrow transplant toxicity in a subject undergoing bone marrow transplant comprising intravenously or orally administering to the subject a therapeutically effective amount of a nitric oxide precursor, whereby bone marrow transplant toxicity is treated or prevented in the subject. 
     
     
         12 - 17 . (canceled) 
     
     
         18 . A method of treating a disorder selected from the group consisting hepatitis, cirrhosis, necrotizing enterocolitis (NEC), Acute Respiratory Distress Syndrome, ethnic specific endothelial dysfunction, erectile dysfunction, asthma, chemotherapy, increased oxidative stress, septic shock, hypoxia, hepatotoxin exposure, or a combination thereof in a subject comprising administering to a subject in need thereof an effective amount of a nitric oxide precursor. 
     
     
         19 . The method of  claim 18 , wherein the administering is intravenously or orally. 
     
     
         20 . The method of  claim 18 , wherein the nitric oxide precursor is selected from the group consisting of citrulline, arginine and combinations thereof. 
     
     
         21 . The method of  claim 18 , wherein the nitric oxide precursor is administered in a dose ranging from about 100 mg to about 30,000 mg. 
     
     
         22 . The method of  claim 21 , wherein the nitric oxide precursor is administered in a dose ranging from about 250 mg to about 1,000 mg. 
     
     
         23 . The method of  claim 18 , wherein the subject is a human. 
     
     
         24 . The method of  claim 18 , wherein the disorder is necrotizing enterocolitis (NEC). 
     
     
         25 - 33 . (canceled) 
     
     
         34 . The method of  claim 18 , wherein the asthma is acute asthma attack. 
     
     
         35 . The method of  claim 18 , wherein the nitric oxide precursor is administered in a dose ranging from about 200 mg/kg, 400 mg/kg, 600 mg/kg, or 800 mg/kg. 
     
     
         36 . A method for treating or preventing pulmonary hypertension comprising administering to a subject in need thereof an effective amount of a nitric oxide precursor.

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