The ability to modify genes and gene expression using various therapeutic techniques has unlocked the potential to treat numerous diseases that were once considered out of reach. Yet many approaches to gene upregulation have significant limitations. By amplifying mRNA to increase healthy gene expression, we believe that we can do better.
Our goal: precise, potent and durable therapeutics that can be programmed to treat diseases where increased protein levels are needed.
We use next-generation sequencing technologies powered by proprietary machine learning algorithms to map regRNAs and cell specific genes they control.
We rapidly generate ASO drug candidates that target regRNA hotspots for maximum gene upregulation.
We design high-potency RNA Amplifiers for safe and effective delivery to target tissues underlying disease.
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