Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Gemini is an intravenously administered, proprietary formulation of phosphorylated hexaacyl disaccharide (PHAD) developed by Revelation Biosciences. It is designed to reduce inflammation-associated damage by reprogramming the innate immune system to respond in a less damaging manner to stressors such as trauma or infection. Gemini has demonstrated pharmacodynamic activity in clinical studies, including upregulation of anti-inflammatory cytokines like IL-10 and reduction of proinflammatory cytokines. It is being developed for multiple indications, including prevention or reduction of acute kidney injury (GEMINI-AKI program), prevention or reduction of post-surgical infection (GEMINI-PSI program), and treatment to slow the progression of chronic kidney disease (GEMINI-CKD program).
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Gemini.