Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Enamptcumab** is a humanized monoclonal antibody developed by Aqualung Therapeutics that specifically neutralizes extracellular nicotinamide phosphoribosyltransferase (eNAMPT), a pro-inflammatory cytokine implicated in acute respiratory distress syndrome (ARDS) and ventilator-induced lung injury (VILI). By binding eNAMPT, it disrupts the eNAMPT/TLR4 inflammatory pathway, inhibiting NFκB activation, reducing cytokine production (e.g., IL-6, TNFα), preserving Akt/mTORC2 signaling, and attenuating lung inflammation, edema, and histological injury. Preclinical studies in rat and porcine ARDS/VILI models demonstrated ~50% reduction in lung injury severity, improved compliance, and lowered serum lactate; Phase 1 trials confirmed safety and dose-proportional pharmacokinetics with a half-life of 17-27 days.[2][4][10][12][16]
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 enamptcumab.