Pro Nephro AKI (NGAL) is now FDA-Cleared     READ MORE

Transforming Care Through Actionable Biomarkers

BioPorto is dedicated to providing clinicians with tools to make impactful changes in patient management; currently, the NGAL biomarker to aid in the risk assessment and diagnosis of acute kidney injury.

Acute Kidney Injury is a Silent Epidemic

The current standard of care for assessing AKI in critically ill patients relies on changes in serum creatinine and urine output, physiologic endpoints that are delayed, non-specific, and impacted by extrarenal
factors such as nutritional status and muscle mass.iii

Empowering Early Intervention

Rapidly detect acute kidney injury with The NGAL Test™. Unlike traditional methods, an NGAL result identifies kidney damage early, guiding interventions with the potential to prevent irreversible damage. Take confident action now.

*The NGAL Test is CE-marked and available for in vitro diagnostic use in the EU. It is registered in Canada, Korea, Israel and other countries.

Revolutionizing Pediatric AKI Risk Assessment

BioPorto welcomes ProNephro AKI (NGAL) to its family of NGAL products in the race against kidney damage – the first FDA-cleared biomarker for pediatric acute kidney injury risk assessment. US commercial availability through Roche Diagnostics is expected in 2025.

*ProNephro AKI is FDA-cleared for use in the US. Commercial availability expected in 2025.

Supporting Research

BioPorto offers a unique range of human and animal NGAL ELISA kits for preclinical animal research and Phase 1 human clinical trials.

Join us in changing the kidney care paradigm

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