Drug intelligence / Profile preview

flopristin + linopristin

Development stage
Phase 2
Lead developer
AstraZeneca
Modality
Small Molecules, Peptides
Administration
Oral
01

Overview

NXL103 is an oral, semisynthetic antibiotic combination consisting of two streptogramins—flopristin (streptogramin A) and linopristin (streptogramin B)—formulated in a 70/30 ratio. Developed by Novexel, NXL103 acts as a protein synthesis inhibitor by binding to the bacterial ribosome, with its two components working synergistically to inhibit bacterial growth. It demonstrates potent bactericidal activity against a broad spectrum of Gram-positive bacteria—including methicillin-resistant *Staphylococcus aureus* (MRSA), vancomycin-resistant enterococci (VRE), and *Streptococcus pneumoniae*—as well as some Gram-negative and anaerobic organisms. NXL103 was primarily developed for the treatment of community-acquired pneumonia and complicated skin and soft tissue infections such as acute bacterial skin and skin structure infections (ABSSSI). Clinical trials showed efficacy comparable to amoxicillin for community-acquired pneumonia, with gastrointestinal intolerance being the most common adverse event[1][3][4][5][6][7].

Other names
linopristin + flopristinNXL101 + NXL102
02

Targets

PTC (50S ribosomal peptidyl transferase center)Neuraminidase

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