Drugs

Development of biomedical products: vaccines, antibodies, gene therapy drugs, etc.

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  • Betusphere Platform

    Platform for developing corpuscular adjuvant-based recombinant protein vaccines. The use of an adjuvant for betulin-based vaccines makes it possible to increase immunogenicity (efficacy, protectiveness), the speed of development and duration of the immune response, optimize the antigen dose, and prevent competition of antigens in combination vaccines.

    Drug
    Indication
    DSCVRY
    Preclinical
    Clinical
    Market
    • Betuvax-CoV-2
      Indication:
      COVID-19
      Clinical
      Indication:

      Primary/booster vaccination SARS-COV-2

      Stage:
      Clinical (primary), Preclinical (booster)
      Description:

      Russia’s first subunit recombinant vaccine based on spherical particles with the surface protein of coronavirus.

      The antigen used is part of the RBD domain of the S protein of coronavirus SARS-CoV-2. It is the RBD domain in response to which the immune system produces the largest number of virus-neutralizing antibodies.

      The Betuvax-CoV-2 vaccine does not contain inactivated or weakened particles of the new SARS-COV-2 coronavirus, does not contain vector viruses (adenovirus, influenza, measles, etc.), does not contain genetic material (RNA or DNA), inorganic adjuvants, so it is designed as a tool for multiple revaccinations, since it potentially does not have any short-term adverse reactions and does not cause excessive antigenic load.

      The Betuvax-CoV-2 vaccine is designed so that it can be quickly optimized for new strains of coronavirus.

    • TetraFluBet
      Indication:
      Influenza
      Clinical
      Indication:

      Influenza vaccination

      Stage:
      Clinical
      Description:

      Quadrivalent subunit influenza vaccine consisting of surface antigens of the influenza virus adsorbed on the adjuvant surface. The drug does not contain preservatives or stabilizing agents that could cause post-vaccination complications.

      The vaccine showed a high safety profile and low reactogenicity in preclinical and clinical trials due to its low antigen content (one vaccine dose contains 5 μg of hemagglutinin from each of the four seasonal vaccine strains).

    • Combi 5V (Nacimbio)
      Indication:
      Influenza + COVID-19
      Preclinical
      Indication:

      Influenza + COVID-19 Combi vaccine

      Stage:
      Preclinical
      Description:

      Combined recombinant vaccine for protection against four seasonal strains of influenza viruses, as well as a component protecting against the SARS-CoV-2 virus.

      The vaccine was developed on the basis of the TetraFluBet and Betuvax-CoV-2 vaccines.

    • Betusphere
      Indication:
      Immunomodulator
      Preclinical
      Indication:

      Immunomodulator

      Stage:
      Preclinical
      Description:

      The company began developing a substance with immunobiological activity. Preclinical studies are currently being completed.

    • RBT-402
      Indication:
      HPV
      DSCVRY
      Indication:

      HPV vaccination

      Stage:
      DSCVRY
      Description:
      A technology platform developed to create recombinant surface proteins of the five current HPV strains: 6, 11, 16, 18, 31.

    • RBT-501
      Indication:
      Allergies
      DSCVRY
      Indication:

      Allergies

      Stage:
      DSCVRY
      Description:
      The company began developing adjuvant recombinant vaccines based on natural allergens: Fel d1 (major feline allergen), Can f5 (major canine allergen), and Der p1 (major house dust mite allergen). The effectiveness of this technology has been proven by extensive clinical, blind, placebo-controlled studies abroad. The use of recombinant allergens will allow us to standardize therapeutic allergens, guaranteeing stable antigen circulation in the blood and the predictable effect of allergen-specific immunotherapy for allergic diseases.

    Developer: Biotechnology Developments, Betuvax
  • Nextgen Platform

    Recombinant plasmid DNA-based gene therapy drugs stimulate the formation and growth of collateral vessels. Indications: treatment of conditions that require the development of collateral circulation.

    Drug
    Indication
    DSCVRY
    Preclinical
    Clinical
    Market
    • Neovasculgen
      Indication:
      Lower Limb Ischemia
      Market
      Indication:

      Lower Limb Ischemia

      Stage:
      Market
      Description:

      The action of the drug is fundamentally different from all known drugs for the treatment of chronic lower limb ischemia (CLI). This is the world’s first gene therapy drug based on the “therapeutic angiogenesis” mechanism (therapeutic vessel growth).

      Neovasculgen stimulates the production of vascular endothelial growth factor VEGF-165, resulting in the growth of new microvasculature at the site of drug administration, which results in better blood supply to the ischemic area.

      Clinically, patients show a more than 5-fold increase in pain-free walking distance (PFWD) and an improvement of such indicators as tissue oxygenation, ankle-brachial index, linear blood flow velocity.

      The drug is included in the “List of Vital and Essential Drugs” and “National and Clinical Guidelines for CLI Treatment.”

    • Neovasculgen
      Indication:
      Diabetic Foot Syndrome
      Clinical
      Indication:

      Diabetic Foot Syndrome

      Stage:
      Clinical
      Description:
      Neovasculgen® is a highly purified super-coiled form of the pCMV-VEGF165 plasmid that encodes the vascular endothelial growth factor (VEGF) under the control of a promoter (DNA control region). This plasmid molecule penetration into the mammalian cells leads to the VEGF production stimulating endothelial cells, which results in the growth of blood vessels (vascularization) at the injection site.

    • Neovasculgen
      Indication:
      Interstitial Cystitis
      Clinical
      Indication:

      Interstitial Cystitis

      Stage:
      Clinical
      Description:
      Neovasculgen® is a highly purified super-coiled form of the pCMV-VEGF165 plasmid that encodes the vascular endothelial growth factor (VEGF) under the control of a promoter (DNA control region). This plasmid molecule penetration into the mammalian cells leads to the VEGF production stimulating endothelial cells, which results in the growth of blood vessels (vascularization) at the injection site.

    • Neovasculgen
      Indication:
      Androgenetic Alopecia
      DSCVRY
      Indication:

      Androgenetic Alopecia

      Stage:
      DSCVRY
      Description:
      Neovasculgen® is a highly purified super-coiled form of the pCMV-VEGF165 plasmid that encodes the vascular endothelial growth factor (VEGF) under the control of a promoter (DNA control region). This plasmid molecule penetration into the mammalian cells leads to the VEGF production stimulating endothelial cells, which results in the growth of blood vessels (vascularization) at the injection site.

    • Neovasculgen
      Indication:
      Peripheral Nerve Injuries
      DSCVRY
      Indication:

      Peripheral Nerve Injuries

      Stage:
      DSCVRY
      Description:
      Neovasculgen® is a highly purified super-coiled form of the pCMV-VEGF165 plasmid that encodes the vascular endothelial growth factor (VEGF) under the control of a promoter (DNA control region). This plasmid molecule penetration into the mammalian cells leads to the VEGF production stimulating endothelial cells, which results in the growth of blood vessels (vascularization) at the injection site.

    Developer: ArtGene Therapeutics , Nextgen
  • Genotarget

    Development of gene therapy drugs for the treatment of rare neuromuscular diseases.

    Drug
    Indication
    DSCVRY
    Preclinical
    Clinical
    Market
    • GT DF 100
      Indication:
      Dysferlinopathy
      Preclinical
      Indication:

      Dysferlinopathy (AAV)

      Stage:
      Preclinical
      Description:
      AAV vector-based drug for the transfer of a fully functional copy of the DYSF gene for treating LGMD R2 (dysferlinopathy, Miyoshi myopathy).

    Developer: Genotarget
  • Proteomarine

    Development of original next-generation biopharmaceuticals based on shark nanobody inhibitors, including drugs for cardiovascular diseases and cancer.

    Drug
    Indication
    DSCVRY
    Preclinical
    Clinical
    Market
    • Shark-based Nanobody (PD-L1 Inhibitor)
      Indication:
      CVD, oncology
      DSCVRY
      Indication:

      CVD, oncology

      Stage:
      DSCVRY
      Description:

      The biopharmaceutical drug binds to PD-L1 to activate the immune system to fight tumor cells.

    Developer: Proteomarine