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Trimeris, Inc. Patents
Assignee:
Trimeris, Inc.
Address:
Durham, NC
No. of patents:
25
Patents:




Patent Number Title Of Patent Date Issued
7456251 HIV fusion inhibitor peptides with improved biological properties November 25, 2008
Provided is an HIV fusion inhibitor peptide having an amino acid sequence of any one of SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, or SEQ ID NO:15; and provided is a pharmaceutical composition comprising a HIV fusion inhibitor peptide and one or mo
7297784 DNA encoding T-1249 and other viral fusion inhibitor peptides useful for treating aids November 20, 2007
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid p
7045552 Pharmaceutical composition for improved administration of HIV gp41-derived peptides, and its use May 16, 2006
Provided is a pharmaceutical composition comprising a solution comprised of synthetic peptide in a final concentration of not less than 70 mg/ml in admixture with a polyol; wherein the synthetic peptide is an HIV fusion inhibitor, and wherein the polyol is in a final concentration of
6951717 Methods and compositions for inhibition of membrane fusion-associated events, including HIV tran October 4, 2005
Parainfluenza virus types 1 to 4 (PIV1 to PIV4) are important human pathogens that cause upper and lower respiratory tract infections, particularly in infants and children. The claimed invention is directed toward novel methods for the inhibition of parainfluenza virus transmission t
6861059 Methods and compositions for treatment of HIV-1 infection using antiviral compounds in simultane March 1, 2005
Novel antiviral combinations for the treatment or prevention of viral infections, in particular, HIV, are disclosed. This new antiviral therapy employs either DP-178 or DP-107, viral fusion inhibitors, in combination with at least one other antiviral therapeutic agent. The combinations o
6750008 Methods and compositions for inhibition of membrane fusion-associated events, including HIV tran June 15, 2004
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention comprise DP178 (SEQ ID:1) peptide corresponding to amino acids 638 to 673 of the HIV-1.sub.LAI gp41 protein, and fragments, analogs and homologs of DP178. The invent
6656906 Hybrid polypeptides with enhanced pharmacokinetic properties December 2, 2003
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid p
6623741 Methods and compositions for inhibition of membrane fusion-associated events including RSV trans September 23, 2003
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention are derived from regions of viral fusion proteins referred to as HR1 and HR2. In particular, the invention relates to peptides referred to herein as DP107 and DP178
6562787 Hybrid polypeptides with enhanced pharmacokinetic properties May 13, 2003
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid p
6541020 Methods and compositions for administration of therapeutic reagents April 1, 2003
Methods and compositions are taught that may be used to administer specific bioactive polypeptides, known as T20 and T1249 to a patient, e.g., as a method of treating a disease or disease state. In particular, the invention teaches carrier hydrogel composition that contain (a) a polymer
6518013 Methods for the inhibition of epstein-barr virus transmission employing anti-viral peptides capa February 11, 2003
Fusion of the viral envelope, or infected cell membranes with uninfected cell membranes, is an essential step in the viral life cycle. Recent studies involving the human immunodeficiency virus type 1(HIV-1) demonstrated that synthetic peptides (designated DP-107 and DP-178) derived f
6479055 Methods for inhibition of membrane fusion-associated events, including respiratory syncytial vir November 12, 2002
The present invention relates to peptides which exhibit potent anti-viral activity. In particular, the invention relates to methods of using such peptides as inhibitory of respiratory syncytial virus ("RSV") transmission to uninfected cells. The peptides used in the methods of the invent
6475491 Treatment of HIV and other viral infections using combinatorial therapy November 5, 2002
Novel antiviral combinations for the treatment or prevention of viral infections, in particular, HIV, are disclosed. This new antiviral therapy employs either DP-178 or DP-107, viral fusion inhibitors, in combination with at least one other antiviral therapeutic agent. The combinations o
6469136 Methods and composition for peptide synthesis October 22, 2002
The present invention relates, first, to methods for the synthesis of peptides referred to as T-1249 and T-1249-like peptides. Such methods utilize solid and liquid phase synthesis procedures to synthesize and combine groups of specific peptide fragments to yield the peptide of inter
6440656 Methods for the inhibition of respiratory syncytial virus transmission August 27, 2002
Fusion of the viral envelope, or infected cell membranes with uninfected cell membranes, is an essential step in the viral life cycle. Recent studies involving the human immunodeficiency virus type 1 (HIV-1) demonstrated that synthetic peptides (designated DP-107 and DP-178) derived
6348568 Hybrid polypeptides with enhanced pharmacokinetic properties February 19, 2002
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid p
6281331 Methods and compositions for peptide synthesis August 28, 2001
The present invention relates, first, to methods for the synthesis of peptides, in particular T-20 (also referred to as "DP-178"; SEQ ID NO:1) and T-20-like peptides. Such methods utilize solid and liquid phase synthesis procedures to synthesize and combine groups of specific peptide
6258782 Hybrid polypeptides with enhanced pharmacokinetic properties July 10, 2001
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid p
6228983 Human respiratory syncytial virus peptides with antifusogenic and antiviral activities May 8, 2001
The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recog
6093794 Isolated peptides derived from the Epstein-Barr virus containing fusion inhibitory domains July 25, 2000
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention comprise DP178 (SEQ ID:1) peptide corresponding to amino acids 638 to 673 of the HIV-1.sub.LAI gp41 protein, and fragments, analogs and homologs of DP178. The invention
6068973 Methods for inhibition of membrane fusion-associated events, including influenza virus May 30, 2000
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention comprise DP178 (SEQ ID:1) peptide corresponding to amino acids 638 to 673 of the HIV-1.sub.LAI gp41 protein, and fragments, analogs and homologs of DP178. The invent
6060065 Compositions for inhibition of membrane fusion-associated events, including influenza virus tran May 9, 2000
The present invention relates to viral peptides referred to as "DP107- and DP178-like" peptides. Specifically, the invention relates to isolated influenza A DP107- and DP178-like peptides which are identified by sequence search motif algorithms. The peptides of the invention exhibit
6054265 Screening assays for compounds that inhibit membrane fusion-associated events April 25, 2000
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention comprise DP178 (SEQ ID:1) peptide corresponding to amino acids 638 to 673 of the HIV-1.sub.LAI gp41 protein, and fragments, analogs and homologs of DP178. The invent
6017536 Simian immunodeficiency virus peptides with antifusogenic and antiviral activities January 25, 2000
The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a simian immunodeficiency virus (SIV) protein. These regions were identified through computer algorithms capable of rec
6013263 Measles virus peptides with antifusogenic and antiviral activities January 11, 2000
The present invention relates to peptides which exhibit potent anti-retroviral activity. The peptides of the invention comprise DP178 (SEQ ID:1) peptide corresponding to amino acids 638 to 673 of the HIV-1.sub.LAI gp41 protein, and fragments, analogs and homologs of DP178. The invent

 
 
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