Report ID: SQMIG35D2145
Report ID:
SQMIG35D2145 |
Region:
Global |
Published Date: March, 2024
Pages:
219
|
Tables:
88 |
Figures:
76
Thermo Fisher's immunoassays for assessing preeclampsia risk were approved by the FDA in May 2023. Preeclampsia risk assessment and clinical management will be aided by these immunoassays, which are the first to be cleared by the FDA and designated as breakthroughs. This represents a major advancement in the treatment of this serious pregnancy condition.
In May 2023, Sera Prognostics Inc., unveiled a series of commercial transformations. With a steadfast commitment to enhancing the well-being of mothers and newborns, the company pioneered innovative pregnancy biomarker information, empowering both doctors and patients alike.
At the 20th World Congress in Fetal Medicine in Valencia, Spain, in June 2023, Diabetomics presented the findings of clinical trials on first-trimester screening and diagnostic support for preeclampsia. The findings showed that the FMF 'Triple' screening test for preterm preeclampsia has significantly increased screening performance with the addition of GlyFn as a supplemental biomarker; nevertheless, additional validation in various populations is required to corroborate these findings.
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Report ID: SQMIG35D2145