Stuck in a Rut - The Magpies Need to Overcome Their Travel Blues
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- By Brittany Stone
- 11 Jul 2026
During a tenure as head of the World Health Organization, a former leader famously stated that all of the “simple” antimicrobials had already been found. The argument was that in addressing the urgent threat of antibiotic-resistant infections, we would struggle to discover new treatments – or conserve the current arsenal – without developing novel approaches of operating. This view proved accurate.
Since the late 2010s, only sixteen antimicrobial agents have gained broad regulatory approval – mostly similar derivatives of medicines currently available and thus unlikely to overcome resistance for long. The creation of novel compounds is a lengthy and financially unattractive endeavor, given that curative medicines are less lucrative as those treating longer-term ailments. The scientific outlook remains bleak.
Nevertheless, the recent announcement of two new regulator-approved antibiotics for gonorrhoea is a welcome development and, importantly, confirms a new way of encouraging development. One of the recently approved medications, a compound called Zoliflodacin, is the result of a unique type of partnership between a global health organization and a drug firm. The public health partnership provided financial support and managed clinical trials to offset costs and clear approval processes. This type of support upfront helps steer the industry towards areas of most pressing global need.
This model and a separate praised revenue guarantee scheme – initiated to guarantee revenue to companies that invest in specific antimicrobials – constitute the best hope of maintaining a dripfeed of new drugs from the current system.
But even hurrying the production of compounds currently in development isn't enough. The new drug is sometimes categorized as a new class of antibiotic, meaning it attacks a component of the infectious bacteria that existing treatments does, theoretically forcing the pathogen to start from zero in evolving a countermeasure to it. Researchers and physicians are grateful to have a new option for gonorrhoea – which has strains resistant to every known antibiotic – but warn that future resistance to this compound is inevitable.
As has grown customary with new antibiotics, exists consequently an debate about whether it should be held in reserve, rationed to extremely drug-resistant cases only – limiting its use to situations where high‑end lab testing is accessible. This sort of prudent approach should be the worldwide norm, but often cannot be implemented readily in many parts of the world.
On a wider scale, it is difficult to see where the flow of additional new antibiotics we need could realistically originate. The former official's statement nodded to the fact that surveying the natural world for natural sources – as with penicillin – has had diminishing returns. Use of AI has been proposed to accelerate the search, although a highly-touted initial discovery found in recent years hasn't yet advanced past preclinical studies. Synthetic drugs, which are mainly or fully lab-created, are constantly in research, but often confront the fundamental rules of chemistry – just because we imagine a compound does not guarantee we can synthesise it easily.
The dominant scientific evaluation is that when it comes to antimicrobials, we must move with great speed indeed just to stay in the current position. Careful, globally managed deployment is the only way to preserve our therapeutic edge. Regrettably, the magnitude of future breakthroughs is likely to seem meager compared with the therapeutic revolution of the previous century.
A software engineer and tech writer passionate about open-source projects and AI advancements.