Pipeline
Project
Targets
Indications
Pesearch
Preclinical Study
Phase I
Phase II
Phase III
NDA
  • Project
    CG-0255 (IV)
    Targets
    P2Y12 Antagonist
    Indications
    Adjunct to percutaneous coronary intervention (PCI), and adjunct to endovascular mechanical recanalization for AIS
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    Phase
    NDA
    CG-0255 (IV)

    CG-0255 is a revolutionary new generation antiplatelet drug targeting P2Y12 receptor.  It is world’s first non-disulfide thiol based prodrug that replies only on esterases for one-step, fast and uniform hydrolytic activation.  It is also world’s first irreversible P2Y12 antagonist for IV injection.  CG-0255 is expected to be approved for percutaneous coronary intervention (PCI), perioperative antiplatelet therapy, perioperative antiplatelet therapy for mechanical thrombectomy in stroke.  CG-0255 fulfils unmet medical needs and can be applied broadly to address various clinical shortcomings.

  • Project
    CG-0255 (PO)
    Targets
    P2Y12 Antagonist
    Indications
    Acute coronary syndrome, recent MI, recent stroke, or established peripheral arterial disease
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    Phase
    NDA
    CG-0255 (PO)

    CG-0255 is a revolutionary new generation antiplatelet drug targeting P2Y12 receptor.  It is world’s first non-disulfide thiol based prodrug that replies only on esterases for one-step, fast and uniform hydrolytic activation.  CG-0255 has been shown to have good dose linearity, minimal individual PK/PD variation in human, and excellent balance between antiplatelet effect and bleeding risk.  CG-0255 is expected to be approved through a special and expedited regulatory process for long term treatment of acute coronary syndrome (ACS), myocardial infarction (MI), stroke, and peripheral arterial disease (PAD).

Project
Targets
Indications
Pesearch
Preclinical Study
Phase I
Phase II
Phase III
NDA
  • Project
    CG-0980
    Targets
    RdRp Inhibitor
    Indications
    RSV/hMPV infection in hospitalized pediatric patients
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    II
    Phase
    III
    NDA
    CG-0980

    CG-0980 is a small molecule direct antiviral drug with broad-spectrum antiviral activity. It is effective against respiratory syncytial virus (RSV), human metapneumovirus (hMPV), and a number of other common respiratory RNA viruses. It has good safety profile and possess potential to be developed into a drug suitable for infants and young children, fulfilling a unmet medical needs.

    RSV is the most common viral pathogen causing acute lower respiratory tract infections in children under 5 worldwide, it is also the leading cause of hospitalization for respiratory tract viral infections in infants and young children. It is estimated that there were approximately 33 million RSV-ALRTI (RSV viral infection with acute lower respiratory tract infections) cases in children under 5 years worldwide in 2019, resulting in approximately 3.6 million hospitalizations and 100,000 deaths. So far, there are no effective antiviral treatments for RSV.  CG-0980 has tremendous clinical potential, its IND application will be submitted in 2024.


  • Project
    CG-0985
    Targets
    RdRp Inhibitor
    Indications
    Broad-spectrum antiviral drug for respiratory infections
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    II
    Phase
    III
    NDA
    CG-0985
    提供信息
  • Project
    CG2021S
    Targets
    siRNA
    Indications
    Functional cure for chronic hepatitis B
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    II
    Phase
    III
    NDA
    CG2021S
    提供信息
  • Project
    CG2021V
    Targets
    Immunoagonist
    Indications
    Functional cure for chronic hepatitis B
    Early
    discovery
    Preclinical
    studies
    Phase
    I
    Phase
    II
    Phase
    III
    NDA
    CG2021V

    According to the recent expert consensus on hepatitis B treatment, neither the currently widely used nucleoside/nucleotide antiviral drugs nor interferons are sufficient to broadly improve the functional cure of hepatitis B. To truly achieve HBV functional cure, it is necessary to combine approaches of direct antiviral, HBV gene expression suppression, and immune reactivation.  These treatment options may be used jointly or sequentially according to conditions of each individual patient in order to achieve the ideal clinical endpoint.  The CG-2021V project is part of a comprehensive strategy for the functional cure of chronic hepatitis B, based on CureGene core platform. It uses innovative mRNA technology to effectively stimulate the body's immune system for immune reactivation, and therefore eliminate hepatitis B virus. This product will be combined with CureGene's siRNA product to form our combination solution for functional cure of chronic hepatitis B.


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