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Funded Projects › FP7

PROFNAIT · Development of a prophylactic treatment for the prevention of fetal/neonatal alloimmune thrombocytopenia (FNAIT)

FP7Status: CLOSED1 August 201231 January 2019EU funding €5,986,000

Objective--The project aims to develop an anti HPA-1a immunoglobulin (IgG), Tromplate® that can prevent post delivery immunisation of the mother against the Human Platelet Antigen-1a (HPA-1a). This prophylactic treatment will prevent Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT) in the fetus/newborn in subsequent pregnancies.FNAIT--FNAIT is a rare but potentially serious condition which affects about 4,000 fetuses and newborns a year in EU-27 and which may result in severe bleeding, intracranial hemorrhage, fetal death or lifelong disability. FNAIT may develop when the mother and the fetus have different platelet surface antigens, most commonly HPA-1a. Transferral of HPA-1a antigen from the fetus may cause immunisation of the mother and the anti-HPA-1a antibodies she develops may in turn destroy the platelets of subsequent HPA-1a positive fetuses/newborns and cause FNAIT. Today, no good treatment of FNAIT exists.Rationale--Previously, it was believed that the pregnant woman develops antibodies early in the first pregnancy with the implication that FNAIT could not be prevented. However, a study conducted by the applicants of more than 100,000 pregnancies revealed that HPA-1a antibody formation most often takes place in association with or after delivery. Therefore, anti-HPA-1a IgG given to the mother shortly after birth should prevent her immune system from generating harmful anti-HPA-1a antibodies. This concept is analogous to the use of anti(D) for Rhesus D prophylaxis.Activities--The project elements: manufacturing of Tromplate® using the process for producing anti(D); screening for HPA-1a negative and pregnant women and clinical Phase II/III studies investigating the efficacy and safety of Tromplate®.Relevance to the work program−The prophylactic Tromplate® treatment has obtained orphan drug status in Europe. FNAIT represents a significant health care expense for the society and a great burden for the affected children and their families.

Consortium · 12 organisations

coordinator

PROPHYLIX PHARMA AS

NO · €2,490,167

participant

UNIVERSITETET I TROMSOE - NORGES ARKTISKE UNIVERSITET

NO · €102,941

participant

LUNDS UNIVERSITET

SE · €113,388

participant

BIOTEST AG

DE · €4,108

participant

FRAUNHOFER GESELLSCHAFT ZUR FORDERUNG DER ANGEWANDTEN FORSCHUNG EV

DE · €624,439

participant

OSLO UNIVERSITETSSYKEHUS HF

NO · €57,965

participant

LARIX AS

DK · €997,069

participant

REGION NORDJYLLAND (NORTH DENMARK REGION)

DK · €83,137

participant

DRK-BLUTSPENDEDIENST BADEN-WURTTEMBERG-HESSEN GGMBH

DE · €901,365

participant

REGION STOCKHOLM

SE · €55,444

participant

UNIVERSITETSSYKEHUSET NORD-NORGE HF

NO · €549,976

participant

REGION SKANE

SE · €6,000

Research fields

View the official record on CORDIS →

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Source: CORDIS, Publications Office of the European Union. Global Research Partnerships surfaces open EU research data to help you find collaborators; we are not affiliated with the European Union.