Zn-c3

Other Medications

US Experimental EU Experimental ES Not available Oral 1 Clinical Trials
WEE1

Description

Zn-c3 (also known as ZN-c3) is an investigational, oral small-molecule inhibitor of WEE1 kinase currently being evaluated in clinical trials for various advanced solid tumors, including colorectal cancer. It is being studied primarily in patients with refractory or advanced cancers, often in combination with other agents such as chemotherapy or targeted therapies. As an experimental agent, it is not yet approved for routine clinical use in CRC, and access is generally limited to clinical trial settings.

Mechanism of Action

Zn-c3 selectively inhibits WEE1, a kinase that regulates the G2/M cell cycle checkpoint and plays a critical role in DNA damage repair. By blocking WEE1, Zn-c3 forces cancer cells—particularly those with defects in other DNA damage response pathways (e.g., TP53 mutations)—to enter mitosis with unrepaired DNA damage, leading to mitotic catastrophe and cell death.

Molecular Targets

Side Effects

Myelosuppression (neutropenia Thrombocytopenia Anemia); nausea; vomiting; fatigue; diarrhea; decreased appetite

Not all side effects are listed. Side effects vary by individual. Always consult your oncologist.

Clinical Trials

NCT05743036 Phase 1
Terminated
ZN-c3 in Adult Participants With Metastatic Colorectal Cancer
United States, Australia, Germany, Hungary, Italy, Poland, Spain