Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Nebacumab is a human IgM monoclonal antibody developed for the treatment of sepsis, specifically targeting Gram-negative bacterial infections. Its mechanism of action involves binding to the lipid A region of endotoxin (lipopolysaccharide/LPS) produced by Gram-negative bacteria. By neutralizing circulating endotoxins and reducing levels of pro-inflammatory cytokines such as tumor necrosis factor-alpha, it was intended to mitigate the excessive inflammatory response that leads to septic shock. Nebacumab was developed by Centocor and marketed under the brand name Centoxin in some European countries in 1991. However, clinical trials failed to demonstrate a reduction in mortality among septic patients, leading to its withdrawal from the market in 1993[1][3][5][6][7].
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 Nebacumab.