RAPID ANTIMICROBIAL SUSCEPTIBILITY TESTING

Faster answers.Less waiting.

We are developing rapid susceptibility testing to shorten the journey from clinical sample to result — bringing clarity to antibiotic decisions sooner.

Technology in validation · Built on over a decade of research

FROM CLINICAL SAMPLES. TOWARDS EARLIER ANSWERS.↓

01 /THE CHALLENGE

Resistance is rising. Answers need to come sooner.

Drug-resistant infections place a growing burden on patients, healthcare systems and economies. Knowing how bacteria respond to antibiotics is an essential part of the response.

01 — RESISTANCE
1 in 6

Infections resistant to antibiotics

Among laboratory-confirmed common bacterial infections worldwide in 2023.

WHO · 2025 report ↗
02 — HUMAN IMPACT
4.7M+

Deaths associated with bacterial AMR

Estimated worldwide in 2021. Associated deaths are distinct from deaths directly attributable to resistance.

WHO · 2026 fact sheet ↗
03 — ECONOMIC BURDEN
US$412B

Projected annual treatment costs

For resistant bacterial infections through 2035, under current levels of action. A projection, not a measured current cost.

WHO · 2026 fact sheet ↗

Our focus: shortening the wait for antimicrobial susceptibility results.

↓

02 /OUR APPROACH

Start with the sample. Read the bacterial response.

We combine rapid bacterial isolation and enrichment with monitoring of bacterial metabolism to determine antimicrobial susceptibility.

01

Isolate & enrich

Recover and concentrate bacteria from clinical samples, preparing them for susceptibility testing.

02

Measure metabolism

Monitor bacterial metabolic activity in response to antibiotics to reveal susceptibility.

03

Deliver earlier insights

Generate susceptibility results with a focus on reducing the full time from sample collection to result.

A technology under validation, with urine and blood samples as our initial focus.

03 /OUR PROGRESS

Research behind us. Possibility ahead.

Preliminary clinical validation shows good categorical agreement with the clinical reference method, alongside substantially shorter sample-to-result turnaround times.

10+

years of foundational research

300+

clinical samples evaluated

Validation in progress. Not yet a commercial product.

From sample collection to result

MEAN TURNAROUND TIME

Urine samples

507h
Hospital workflow50 h
Metallix7 h

Blood samples

10013h
Hospital workflow100 h
Metallix13 h

The clock starts at sample collection — not at blood culture positivity.

About these validation results

Source: preliminary clinical validation data supplied by the Metallix team, covering more than 300 clinical samples. Times shown are sample-type mean turnaround times from collection to susceptibility result; comparator times were measured using the hospital’s existing workflow. These are preliminary observations under the evaluated conditions, not guaranteed performance for every sample. Further validation and product development are ongoing.

04 /LET’S MOVE FORWARD

Bring the next chapter closer. Together.

We welcome industry partners and investors who share our ambition to advance rapid susceptibility testing, alongside clinical collaborators for the next stage of validation.

info@metallixmed.com