


SynNeogen® is the world's first engineered murine Fc chimeric protein vaccine platform, powered by the dual engines of AI-driven antigen selection and Fc-mediated precision delivery. The platform leverages AI to identify tumor- or virus-specific T-cell epitopes, and integrates engineered heterologous Fc with glyco-engineering modifications. This design mimics natural immune processes by enabling Fc-mediated, dendritic cell (DC)-targeted delivery of antigens, thereby inducing durable, multi-epitope T-cell responses.
Pipeline
A pipeline with significant clinical demand and global competitive strength.Tumor
Virus infection
FDA Fast Track Approved
·KMV002 (IPT-PAP, IND-ready): A first-in-class immune-priming therapeutic for metastatic castration-resistant prostate cancer (mCRPC), engineered to convert prostate tumors from immune-cold to immune-responsive and enhance the activity of checkpoint inhibitors, AR-targeted agents, radioligands, and emerging modalities.
KMV002 is an investigational therapeutic cancer vaccine currently under clinical development and has not been approved by any regulatory authority.
At this time, ChimiVac does not offer expanded access (also known as compassionate use) to KMV002 outside of authorized clinical trials.
This policy is based on several considerations, including:
·Limited clinical safety information currently available;
·The need to complete ongoing clinical development;
·Limited manufacturing supply;
·The importance of ensuring patient access through controlled clinical studies.
·ChimiVac periodically reviews this policy as clinical development progresses.
Physicians seeking additional information may contact:
Medical Affairs
ChimiVac, Inc.
Email: medical@chimivac.com
Last Updated: October 2026
·SN2001 (IPT-HBV, Phase I): A multi-epitope immune-restoring therapeutic for chronic HBV designed to re-establish functional antiviral immunity in patient populations with profound immune exhaustion.
R&D Centre



Disclaimer: The products mentioned on this page are currently in the clinical research stage and have not yet received marketing approval from any national drug regulatory authority. The content provided here is for reference only and does not constitute a promise or guarantee regarding product efficacy. Development progress may change due to various factors; please refer to official announcements for the most accurate information.