The study will include 40 children with suspected elevated levels of bilirubin (risk of jaundice), where blood tests have to be taken.
The existing point-of-care (POC) analysis methods for bilirubin assessment employ transcutaneous measurement or blood gas analyzers, but these methods fail to address the needs of all infants. The reason is that transcutaneous measurement is only viable up to a certain bilirubin level and fails to generate reliable results above that. Blood gas analyzers for bilirubin assessment do not reveal deteriorations of the sample such as haemolysis, which may result in erroneous measurements and clinically unreliable analysis results. To detect that, a traditional laboratory analysis is required, with all the disadvantages that entails: more blood is needed, it takes longer time and the laboratory staff must perform the task manually.
Calmark Neo-Bilirubin provides faster results than laboratory analysis and requires lower quantities of blood. Contrary to blood gas analyzers, Calmark's product alerts the user if the blood sample is damaged.
“It is really gratifying that we have now been able to include the first patient in the study on Neo-Bilirubin,” says Emma Lif, Clinical Director at Calmark. “The study's principal investigator, Cecilia Pegelow Halvorsen, and her team at Södersjukhuset have made a remarkable job to set this in motion, and I would like to extend my gratitude to them for their commitment!”
The study is conducted in cooperation with the research unit, which is not receiving special compensation for it.
Every care has been taken in the translation of this document. In the event of discrepancies, the Swedish original will supersede the English translation.
This information is information that Calmark Sweden AB (publ) is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact person set out above, on 23 December 2019, 11:50 CET.