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Cenyx Biotech, Inc.
- Ownership
- Private
- Development stage
- Other
Overview
Cenyx Biotech is advancing a first-in-class cerium oxide-based nanozyme, CX213, for SAH-induced inflammation. The candidate has received FDA IND approval and orphan drug designation. Phase I trials are set to begin in the US with expedited regulatory strategies targeting commercialization by ~2028. Preclinical data show superior ROS-scavenging ability compared to existing products. A second asset, CX301 for AKI, is approaching IND submission/approval by mid-to-late 2025. Several additional programs remain confidential.
- Therapeutic areas
- ImmunologyNephrologyNeurology
- Modalities
- Nanozymes (cerium oxide-based and non-CeO2 nanozymes)
- Industry
- Biotech
Drug pipeline
4 assets3 more assets in the full pipeline.
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