



XNW4107 is a broad spectrum, best-in-class BLI inhibitor of the diazabicyclooctane (DBO) class for all three classes of A/C/D SBL. XNW4107 has successfully completed Phase III registration study in HABP/VABP and is currently at NDA stage.


XNW5004 is a best-in-class selective EZH2 inhibitor. In September 2024, XNW5004 was granted BTD (Breakthrough Therapy Designation) by CDE for relapsed or refractory peripheral T-cell lymphoma (PTCL). Pivotal studies in PTCL are ongoing.
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XNW27 and XNW28 are topoi-based ADCs, both programs are currently in Phase III studies, with superior efficacy and safety observed across a broad range of solid tumors.
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XNW27 and XNW28 are topoi-based ADCs, both programs are currently in Phase III studies, with superior efficacy and safety observed across a broad range of solid tumors.
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XNW29 is a first-in-class PARG inhibitor entering Phase I clinical study. In preclinical studies, XNW29 has demonstrated robust efficacy, excellent PK properties and good safety profile.
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XNW34 is a novel heterobifunctional degrader discovered through our TPD platform. The lead asset is currently in IND-enabling studies, with high oral bioavailability, outstanding in vivo efficacy, and manageable AE profile observed in preclinical studies
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XNW4107 is a broad spectrum, best-in-class BLI inhibitor of the diazabicyclooctane (DBO) class for all three classes of A/C/D SBL. XNW4107 has successfully completed Phase III registration study in HABP/VABP and is currently at NDA stage.


XNW5004 is a best-in-class selective EZH2 inhibitor. In September 2024, XNW5004 was granted BTD (Breakthrough Therapy Designation) by CDE for relapsed or refractory peripheral T-cell lymphoma (PTCL). Pivotal studies in PTCL are ongoing.
Contact us



XNW27 and XNW28 are topoi-based ADCs, both programs are currently in Phase III studies, with superior efficacy and safety observed across a broad range of solid tumors.
Contact us

XNW27 and XNW28 are topoi-based ADCs, both programs are currently in Phase III studies, with superior efficacy and safety observed across a broad range of solid tumors.
Contact us



XNW29 is a first-in-class PARG inhibitor entering Phase I clinical study. In preclinical studies, XNW29 has demonstrated robust efficacy, excellent PK properties and good safety profile.
Contact us

XNW34 is a novel heterobifunctional degrader discovered through our TPD platform. The lead asset is currently in IND-enabling studies, with high oral bioavailability, outstanding in vivo efficacy, and manageable AE profile observed in preclinical studies
Contact us