Small molecule · Inhibitor of beta-lactamase · developed by Roerig
Sulbactam is a semi-synthetic beta-lactamase inhibitor that irreversibly binds to bacterial beta-lactamase, blocking its activity and preventing degradation of beta-lactam antibiotics. Combined with ampicillin or other beta-lactam agents, it treats infections caused by beta-lactamase-producing bacteria in skin, intra-abdominal, and gynecological sites. It is also studied in non-tuberculous mycobacterial infections.
Summary written with AI from the sources listed at the end of this page.
From the indications section of the FDA label (version of Jul 10, 2026). Read the full label for the exact wording, limitations and safety information.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT07485010 | Phase 2 | Mycobacterium Abscessus Pulmonary Disease | Not yet recruiting | INVA |
| NCT06801223 | Phase 1 | Acinetobacter Baumannii-calcoaceticus Complex Infection (ABC) | Recruiting | INVA |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Mycobacterium Abscessus InfectionMycobacterium Abscessus Pulmonary DiseaseNon-Tuberculous Mycobacteria Pulmonary DiseaseNon-Tuberculous Mycobacterial (NTM) Infections
Updated Oct 3, 2026.