Who we are

Sironax is an emerging leader in the discovery and development of transformational therapies that address neurodegenerative and muscular degenerative diseases affecting longevity. Today, the majority of treatments for these diseases are palliative, with a focus on alleviating symptoms alone. As pioneers in the science surrounding programmed cell death mechanisms and their connection to age-related degenerative diseases, Sironax was co-founded in 2017 by Dr. Xiaodong Wang and Dr. Zhiyuan Zhang, who recognized the growing need for therapies that could directly address disease pathology.

Since our founding, we have been developing our pathway-driven portfolio strategy which has enabled us to establish a pipeline of novel therapies that address a wide range of degenerative diseases affecting longevity and underlying mechanisms, including regulated cell death, NAD+ pathway modulations, neuroprotective pathways, neuroinflammation, among others. To date, our pipeline contains three innovative programs spanning small and large molecules, all of which are global first-in-class or front-runners. Our lead RIPK1 program is comprised of several chemically differentiated small molecule inhibitors, including SIR9900 and SIR2446, both completed Phase 1a studies in healthy volunteers with robust target engagement and well-tolerated safety profile. Another key program is an axon protection small molecule, which has best-in-class potential, driven by the intrinsic differentiation in inhibitory mechanism. It is currently in Phase 1a study, and preclinical evidence demonstrates strong potential as a transformative therapy for ALS and other neurodegenerative diseases. In parallel, we continue to expand our R&D footprint, with plans to advance additional programs into the clinic over the next several years.

With operations in the United States, China, Switzerland, and Australia,, Sironax presently has 170 employees and is growing as we continue to build our global team of highly skilled chemists, biologists, manufacturing experts, biomarker scientists and clinicians. Along with decades of experience in global pharmaceutical R&D, our team shares a collective vision of shifting the treatment paradigm for disease affecting longevity to ultimately improve the lives of millions of patients and their families around the world.

Mission
We are an emerging leader at the forefront of innovating transformational therapies that address diseases affecting longevity, diseases requiring supportive care, and certain rare diseases.
Vision
We aim to shift the treatment paradigm for degenerative diseases affecting longevity to improve the lives of millions of patients and their families around the world.