The Global Antibiotic Research and Development Partnership (GARDP) is looking into the potential of an older antibiotic used exclusively in veterinary medicine to treat highly drug-resistant infections in people.
GARDP said today that it has acquired all data and licensing rights for apramycin, an aminoglycoside antibiotic introduced in the early 1980s to treat gram-negative bacterial infections in animals. Bought from Swiss drugmaker Juvabis AG after it closed in 2025, the drug has shown potential for human use in preclinical trials.
Apramycin is one of several therapies GARDP is evaluating for drug-resistant gram-negative bacteria, which are a significant driver of deaths caused by bacterial infections and are becoming increasingly resistant to antibiotics. Several gram-negative species have been targeted by the World Health Organizations as “priority pathogens” for antibiotic development.
Phase 1 study planned
GARDP officials say apramycin’s distinct chemical structure enables it to evade the resistance mechanisms that undermine other aminoglycoside antibiotics. A phase 1 study to assess safety and pharmacokinetics is planned for 2027.
“With this project, GARDP is reviving research into a promising antibiotic that had stalled in early-stage development,” Manica Balasegaram, MRCP, MSc, GARDP’s executive director, said in a news release. “Building on early research, GARDP’s studies will now evaluate whether apramycin could become an affordable and effective treatment for increasingly dangerous superbugs affecting people around the world.”