Pipeline
Field
Project No.
Target spot
Candidate Compound
IND
Clinical Phase I
Clinical Phase II
Indication
Oncology
KBD[****]
DNAPK
Oncology
KBD1921
PARP7
Immuno-oncology (I/O) Combination Therapy
Oncology
KBD111
PARP1
Long-Acting CNS (Central Nervous System)
Oncology
KBD881
Undisclosed
Radiopharmaceuticals (RPT)
Oncology
KBD991
Undisclosed
Radiopharmaceuticals (RPT)
Autoimmunity
KBD4409
TLR
Systemic Lupus Erythematosus (SLE)
Autoimmunity
KBD031
Undisclosed
Inflammatory Metabolic Diseases (IMD)
Autoimmunity
KBD151
Undisclosed
Inflammatory Skin Diseases / Dermatological Conditions
Anti-aging
KBD171
Undisclosed
Alzheimer's Disease (AD)
Anti-aging
KBD102
Undisclosed
Alzheimer's Disease (AD)
Anti-aging
KBD081
Undisclosed
Obesity Management & Muscle Preservation
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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