Last reviewed · How we verify

Pathogen reduction process

Etablissement Français du Sang · FDA-approved active Biologic

A pathogen reduction technology that inactivates viruses, bacteria, and other pathogens in blood products through chemical or physical treatment to improve transfusion safety.

A pathogen reduction process inactivates viruses, bacteria, and other pathogens in blood products through physical or chemical treatment to improve transfusion safety. Used for Reduction of transfusion-transmitted viral infections in plasma, Reduction of transfusion-transmitted viral and bacterial infections in platelet concentrates, Reduction of transfusion-transmitted infections in red blood cell products.

At a glance

Generic namePathogen reduction process
SponsorEtablissement Français du Sang
Drug classBlood product safety technology
ModalityBiologic
Therapeutic areaHematology / Transfusion Medicine
PhaseFDA-approved

Mechanism of action

Pathogen reduction processes use methods such as photochemical treatment (e.g., with psoralens and UV light) or other inactivation techniques to neutralize a broad spectrum of pathogens including enveloped and non-enveloped viruses, bacteria, and parasites in blood components. This reduces the risk of transfusion-transmitted infections while maintaining the hemostatic function of the treated blood product.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: