news release rytvel antenatal suppression of ... release rytvela totally prevents fetal organ injury...

2
NEWS RELEASE RYTVELA totally prevents fetal organ injury in inflammatory-induced PTB in mice Rytvela – new treatment paradigm for preterm birth (PTB) and ensued consequences Montreal, Canada, February 16, 2017 RYTVEL Biotech is pleased to announce that the article: Antenatal suppression of interleukin-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in mice was published in the Journal of Immunology. See below for information about the article. Mathieu Nadeau-Vallée, Peck-Yin Chin, Lydia Belarbi, Marie-Ève Brien, Sheetal Pundir, Martin H. Berryer, Alexandra Beaudry-Richard, Ankush Madaan, David J. Sharkey, Alexis Lupien-Meilleur, Xin Hou, Christiane Quiniou, Ines Boufaied, Jean-Sebastien Joyal, William D. Lubell, David M. Olson, Sarah A. Robertson, Sylvie Girard and Sylvain Chemtob. In a previous article, published in September 2015 in the same journal, the authors have demonstrated that Rytvela reduces utero-placental inflammation and is efficacious to restore normal term for birth, and significantly reduces newborn death yielding normal growth trajectory. These data came from three different blinded, separate and independent studies of PTB induces either by IL-1, LPS or LTA. The new publication uses the same design to the previous one but concentrates on neonatal death and outcome, with focus on brain, lungs and gut. The authors show that Rytvela completely protects fetal/newborn organs from the inflammatory in utero insult. It should be highlighted that brain function assessed by visual-evoked potential was totally preserved in animals treated with Rytvela (versus markedly affected controls). Rytvela is a new efficient first in class treatment of the cause and ensuing serious consequences of preterm birth. We are again very encouraged with these new results which focus on fetal outcome, the main problem of PTB, said Sylvain Chemtob, MD, PhD, co-founder of Rytvel Biotech and researcher at CHU Sainte-Justine. Preterm birth (PTB) is the primary cause of mortality of newborn and long term health disability mainly respiratory distress syndrome, bronchopulmonary dysplasia, necrotizing enterocolitis, retinopathy of prematurity and brain hemorrhage, and there are no effective treatment today that addresses critically important utero-placental inflammation to the placenta and fetus. Rytvela offers not only to prolong gestation by allowing increased maturation of the fetus, but also reduces neonatal mortality and improves fetal/neonatal outcome, most importantly regarding neuro-development. This is a first . The article Antenatal suppression of interleukin-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in miceis available at https://rytvel.com/news-publications-and-credentials/, below the news releases. About RYTVEL Biotech and Rytvela RYTVEL Biotech will be the first company exploring a new paradigm therapy to develop Rytvela, an effective drug to end preterm birth to the benefit of women and newborns. Rytvela (a linear 7 amino acid

Upload: lyhanh

Post on 27-Mar-2018

216 views

Category:

Documents


2 download

TRANSCRIPT

NEWSRELEASE

RYTVELAtotallypreventsfetalorganinjuryininflammatory-inducedPTBinmiceRytvela–newtreatmentparadigmforpretermbirth(PTB)andensuedconsequences

Montreal,Canada,February16,2017–RYTVELBiotechispleasedtoannouncethatthearticle:Antenatal suppressionof interleukin-1protectsagainst inflammation-induced fetal injuryandimproves neonatal and developmental outcomes in mice was published in the Journal ofImmunology.Seebelowforinformationaboutthearticle.

MathieuNadeau-Vallée,Peck-YinChin, LydiaBelarbi,Marie-ÈveBrien,SheetalPundir,MartinH.Berryer,AlexandraBeaudry-Richard, Ankush Madaan, David J. Sharkey, Alexis Lupien-Meilleur, Xin Hou, Christiane Quiniou, InesBoufaied, Jean-Sebastien Joyal, William D. Lubell, David M. Olson, Sarah A. Robertson, Sylvie Girard and SylvainChemtob.

In a previous article, published in September 2015 in the same journal, the authors havedemonstrated that Rytvela reduces utero-placental inflammation and is efficacious to restorenormaltermforbirth,andsignificantlyreducesnewborndeathyieldingnormalgrowthtrajectory.

Thesedatacamefromthreedifferentblinded,separateandindependentstudiesofPTBinduceseitherbyIL-1,LPSorLTA.

The new publication uses the same design to the previous one but concentrates on neonataldeathandoutcome,withfocusonbrain,lungsandgut.TheauthorsshowthatRytvelacompletelyprotectsfetal/newbornorgansfromtheinflammatoryinuteroinsult.Itshouldbehighlightedthatbrainfunctionassessedbyvisual-evokedpotentialwastotallypreservedinanimalstreatedwithRytvela(versusmarkedlyaffectedcontrols).

Rytvelaisanewefficientfirstinclasstreatmentofthecauseandensuingseriousconsequencesofpretermbirth.

“Weareagainveryencouragedwiththesenewresultswhichfocusonfetaloutcome,themainproblemofPTB,”saidSylvainChemtob,MD,PhD,co-founderofRytvelBiotechandresearcheratCHUSainte-Justine.“Pretermbirth(PTB) istheprimarycauseofmortalityofnewbornandlongterm health disability mainly respiratory distress syndrome, bronchopulmonary dysplasia,necrotizing enterocolitis, retinopathy of prematurity and brain hemorrhage, and there are noeffectivetreatmenttodaythataddressescriticallyimportantutero-placentalinflammationtotheplacentaandfetus.Rytvelaoffersnotonlytoprolonggestationbyallowingincreasedmaturationof the fetus, but also reduces neonatal mortality and improves fetal/neonatal outcome, mostimportantlyregardingneuro-development.Thisisafirst”.The article “Antenatal suppression of interleukin-1 protects against inflammation-induced fetalinjury and improves neonatal and developmental outcomes in mice” is available athttps://rytvel.com/news-publications-and-credentials/,belowthenewsreleases.

AboutRYTVELBiotechandRytvelaRYTVEL Biotech will be the first company exploring a new paradigm therapy to developRytvela, aneffectivedrugtoendpretermbirthtothebenefitofwomenandnewborns.Rytvela(alinear7aminoacid

peptide)isthefirstsmalldrugcandidateselectivetothemajorpro-inflammatoryinterleukin-1receptor.Pre-clinicalstudieshavebeencorroboratedbythreeindependentacademiclaboratories(UofMontreal,U of Alberta in Canada, andU of Adelaide, Australia). These blinded studies performed separately andindependently demonstrate that Rytvela suppresses utero-placental inflammation, significantlyreduces/suppressespretermbirth(PTB),newborndeathandpreventsmajororgandisruptionincludingofbrain,yieldingnormalgrowthtrajectory.RytvelawasinventedbyDrSylvainChemtobandhisteamattheCHUSainte-JustineResearchCenterinMontreal,Canada.www.rytvel.comAbouttheCHUSainte-JustineResearchCenterCHUSainte-JustineResearchCenterisaleadingmother-childresearchinstitutionaffiliatedwithUniversitédeMontréal.Itbringstogethermorethan200researchinvestigators,includingover90clinician-scientists,as well as 385 graduate and postgraduate students focused on finding innovative prevention means,fasterandlessinvasivetreatments,aswellaspersonalizedapproachestomedicine.TheCenterispartofCHU Sainte-Justine, which is the largestmother-child center in Canada and second pediatric center inNorthAmerica.www.research.chusj.orgAboutPTB(Pretermbirth)PTB isdefinedasbirthoccurringbefore37weeksofgestationandbefore32weeks forearlypre-term.PTBoccursin~10%ofbirths(~550,000inNorthAmerica).EarlyPTBin2to3%ofbirth.ThemajorcauseofPTB isutero-placental inflammation.The consequencesarenewborndeath (more than1millionperyearworldwide), severe life-longhealthhandicaps especially tobrain, lungs and cardiovascular system.The current treatments, namely tocolytic agents have no or very little efficacy, and none of themaddressestheutero-placentalinflammation.ThecostsrelatedtoPTBintheUSAwerereportedin2017tobe$40billion/year.AbouttheJournalofimmunologyThe Journalof Immunology (The JI) publishesnovel,peer-reviewed findings inall areasofexperimentalimmunology, including innateandadaptive immunity, inflammation,hostdefense, clinical immunology,autoimmunityandmore.TheJIispublishedbyTheAmericanAssociationofImmunologists(AAI)andhasanimpactfactorof5.22.

MediaContact:DanielGranger,L.LL.,MBA,APR,FSCRP,IAST.+1514840-7990M.+1514232-1556daniel.granger@acjcommunication.comACJCommunicationScientific,FinancingandBDContacts:JeanPaulCastaigneMD,[email protected]+1514518-5500

SylvainChemtobMD,[email protected]+1514585-4604