Clinical trials
Full profile accessFollow clinical development from trial design and recruitment through results.
- Trial phase
- Status
- Readouts
Company intelligence / Profile preview
Codexis has demonstrated that its proprietary enzyme engineering platforms can enable scalable, efficient, and greener manufacturing of small molecule APIs and siRNA therapeutics. Its ECO Synthesis™ platform has been validated by multiple CDMOs to reduce purification costs, improve process performance, and control stereochemistry in oligonucleotide synthesis. The company’s enzymes have enabled the manufacture of blockbuster drugs such as sitagliptin ("Januvia"), atorvastatin ("Lipitor"), and nirmatrelvir ("Paxlovid"). Recent presentations at TIDES USA highlighted reproducibility and process simplification for siRNA production. Codexis does not develop its own therapeutic pipeline but enables pharmaceutical companies to manufacture their products more efficiently.
Beyond the preview
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Follow clinical development from trial design and recruitment through results.
Explore licensing agreements, acquisitions, and the assets behind each deal.
Trace financing activity and the investors behind a company’s development.
Compare peer pipelines by target, modality, and therapeutic area.
Explore technology platforms and the patent landscape around relevant assets.
Connect company news and source material to the questions you’re investigating.
See how Gosset can support your research on CODEIS.