Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
VBI-1 is an investigational cardiovascular support fluid developed by Vivacelle Bio. It is designed for the treatment of patients experiencing emergently life-threatening hypovolemia, such as severe blood loss (hemorrhagic shock) and potentially other critical conditions like reperfusion injury. VBI-1 represents a refined version of Vivacelle Bio’s earlier product, VBI-S. Its mechanism involves modulating nitric oxide bioavailability in the microcirculation—absorbing excess nitric oxide where it is overproduced and releasing it where levels are insufficient—thereby redistributing nitric oxide to promote survival rather than mortality. This approach aims to increase mean arterial pressure, reduce inflammation, and improve multi-organ function in critically ill patients[2][9]. As of early 2019, the FDA granted IND clearance for a phase IIa clinical trial evaluating its safety and efficacy after blood loss[4][9].
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 VBI-1.