Pipeline
Field
Project No.
Target spot
Indication
Discovery
Lead Compound
Candidate Compound
IND
Phase la Clinical Trial
Phase lb Clinical Trial
Clinical Phase II
Clinical Phase III
Oncology
KBD1921
PARP7
Solid Tumor
Monotherapy
Combination Therapy
Oncology
KBD041
FGFR2
Solid Tumor
Oncology
KBD061
Undisclosed
Solid Tumor
DNA Damage
KBD111
PARP1
Solid Tumor
Inflammatory immunity
KBD031
NLRP3
Inflammatory Diseases
Inflammatory immunity
KBD051
TLR7/8
Autoimmune Diseases
Inflammatory immunity
KBD141
Undisclosed
Cutaneous inflammation
Inflammatory immunity
KBD151
Undisclosed
Cutaneous inflammation
Anti-aging
KBD091
Undisclosed
Aging-related
Tumor Immunity
DNA Damage
Tumor Immunity
Immuno-oncology represents a form of cancer treatment that harnesses the power of the body's own immune system to potentially prevent, control, and eliminate cancer. The rapid progress of modern immunotherapeutics meets several clinical needs to a certain extent. However, there are still some limitations.
For instance, the proportion of cancer patients who may potentially benefit from and respond to PD-1/PD-L1 inhibitors is generally not more than 30%, and the occurrence of acquired drug resistance is relatively common. For cold tumors (such as tumors lacking T cell infiltration) or tumors with immunosuppressive tumor microenvironments (TME), the response rate of current immunotherapeutics is relatively low. Additionally, issues such as high therapy costs and inconvenient administration methods also exist.
To address these challenges, Baiyu is exploring new therapeutic modalities to potentially activate the immune microenvironment and counter multiple tumor escape mechanisms, aiming to overcome some of the limitations of current immunotherapy.
DNA Damage
DNA damage is a ubiquitous life phenomenon. Cells are constantly confronted with damage to their DNA that can stem from endogenous processes such as DNA replication stress or exogenous exposures like ionizing radiation and chemotherapy drugs. Failure to repair this damage can have catastrophic cellular consequences.
To counter this threat, cells have developed intricate repair mechanisms to address the diverse types of possible DNA lesions that emerge. Collectively known as the DNA damage response (DDR), these mechanisms detect DNA damage and mediate its repair. Most current chemotherapy and radiation treatments operate by damaging DNA. Upregulation of the DDR pathway provides tumor cells with a means to evade damage and resist death. Thus, combining chemotherapy and/or radiotherapy with drugs that target DNA repair mechanisms holds promise in potentially overcoming cancer's resistance to treatment.
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