Pipeline
Project No
Area
Target spot
Indication
Preclinical
IND
Clinical Phase I
Clinical Phase II
Clinical Phase III
NDA
KBD101
DNA Damage
DNA-PK
Glioma
KBD111
Oncology
Undisclosed
Solid Tumor
BY1921
Oncology
PARP7
Solid Tumor
Monotherapy
Combination Therapy
KBD041
Oncology
Undisclosed
Solid Tumor
KBD061
Oncology
Undisclosed
Solid Tumor
KBD031
Inflammatory immunity
Undisclosed
Inflammatory Diseases
KBD051
Inflammatory immunity
Undisclosed
Autoimmune Diseases
KBD121
Inflammatory immunity
Undisclosed
Cutaneous inflammation
KBD091
Anti-aging
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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