Patent classifications
A61P31/06
Pharmaceutical composition comprising a polymeric carrier cargo complex and at least one protein or peptide antigen
The present invention is directed to a pharmaceutical composition including (e.g. for use as an adjuvant) a polymeric carrier cargo complex, comprising as a carrier a polymeric carrier formed by disulfide-crosslinked cationic components; and as a cargo at least one nucleic acid molecule, and at least one antigen that is selected from an antigen from a pathogen associated with infectious disease; an antigen associated with allergy or allergic disease; an antigen associated with autoimmune disease; or an antigen associated with a cancer or tumour disease, or in each case a fragment, variant and/or derivative of said antigen. The pharmaceutical composition allows for efficient induction of an adaptive immune response directed against said antigen. The present invention furthermore provides kits, as well as the use of the pharmaceutical composition or the kit as a vaccine, particularly in the treatment of infectious diseases, allergies, autoimmune diseases and tumour or cancer diseases.
Tuberculosis compositions and methods of treating or preventing tuberculosis
The present disclosure provides fusion proteins comprising Mycobacterium tuberculosis (Mtb) antigens, nucleic acid molecules encoding the same, vectors comprising nucleic acid molecules, compositions comprising the same, and methods of eliciting an immune response against tuberculosis.
Tuberculosis compositions and methods of treating or preventing tuberculosis
The present disclosure provides fusion proteins comprising Mycobacterium tuberculosis (Mtb) antigens, nucleic acid molecules encoding the same, vectors comprising nucleic acid molecules, compositions comprising the same, and methods of eliciting an immune response against tuberculosis.
COMBINATION THERAPY FOR TREATING COVID-19
Methods for treating SARS-CoV-2 infection in a subject in need thereof are described. Methods for ameliorating symptoms of COVID-19 disease due to SARS-CoV-2 infection and are also described. The methods comprise administering to the subject an antiviral agent, a nucleoside reverse transcriptase inhibitor, an agent for treating tuberculosis, an agent for treating fever or systemic autoimmune disease with multisystem involvement, and an agent that acts as a bronchodilator or a bronchodilator and cough suppressant, expectorant combination.
COMBINATION THERAPY FOR TREATING COVID-19
Methods for treating SARS-CoV-2 infection in a subject in need thereof are described. Methods for ameliorating symptoms of COVID-19 disease due to SARS-CoV-2 infection and are also described. The methods comprise administering to the subject an antiviral agent, a nucleoside reverse transcriptase inhibitor, an agent for treating tuberculosis, an agent for treating fever or systemic autoimmune disease with multisystem involvement, and an agent that acts as a bronchodilator or a bronchodilator and cough suppressant, expectorant combination.
COMPOSITION AND METHOD FOR HIP1-TARGETING INHIBITOR COMPOUNDS
Provided herein is an inhibitor compound targeting Hip1, with the inhibitor compound comprising a tripeptide targeting sequence that directs the compound to the active site of Hip1 and a C-terminal electrophilic warhead conjugated to the targeting sequence, the warhead configured to inactive the enzyme.
COMPOSITION AND METHOD FOR HIP1-TARGETING INHIBITOR COMPOUNDS
Provided herein is an inhibitor compound targeting Hip1, with the inhibitor compound comprising a tripeptide targeting sequence that directs the compound to the active site of Hip1 and a C-terminal electrophilic warhead conjugated to the targeting sequence, the warhead configured to inactive the enzyme.
Parainfluenza virus 5 based vaccines
The present invention provides safe, stable, efficacious, and cost-effective vaccines based on viral expression vectors that include a parainfluenza virus 5 (PIV5) genome including a heterologous nucleotide sequence expressing a heterologous polypeptide.
Parainfluenza virus 5 based vaccines
The present invention provides safe, stable, efficacious, and cost-effective vaccines based on viral expression vectors that include a parainfluenza virus 5 (PIV5) genome including a heterologous nucleotide sequence expressing a heterologous polypeptide.
NUCLEIC ACIDS COMPRISING FORMULA (NuGlXmGnNv)a AND DERIVATIVES THEREOF AS IMMUNOSTIMULATING AGENT/ADJUVANT
The present invention relates to nucleic acids of the general formula (I): (N.sub.uG.sub.lX.sub.mG.sub.nN.sub.v).sub.a and derivatives thereof as an immunostimulating agent/adjuvant and to compositions containing same, optionally comprising an additional adjuvant. The present invention furthermore relates to a pharmaceutical composition or to a vaccine, each containing nucleic acids of formula (I) above and/or derivatives thereof as an immunostimulating agent, and optionally at least one additional pharmaceutically active component, e.g. an antigenic agent. The present invention relates likewise to the use of the pharmaceutical composition or of the vaccine for the treatment of cancer diseases, infectious diseases, allergies and autoimmune diseases etc. Likewise, the present invention includes the use of nucleic acids of the general formula (I): (N.sub.uG.sub.lX.sub.mG.sub.nN.sub.v).sub.a and/or derivatives thereof for the preparation of a pharmaceutical composition for the treatment of such diseases.