Okay. afternoon. for Thanks and Thanks this Brian good joining us afternoon everyone.
time. our this can you at ahead is business of in working see would where recovery be As from thought the our is results, strategy and we it our
the demand have COVID-XX in COVID-XX, substantial business and significant to innovative our continue first the rebound repair recently which As face to in we continues our you presence. for quarter will for hear bodes we in well continue products. the and remained build aortic impacted business launched our future. a made We've of resilient has progress believe see especially be does Europe where to by But
accelerate for quarter constant growth initiatives from invest to basis When on factors coupled of the We the forma with we last achieved in also anticipated programs quarter Unfortunately, starting to pro to revenue headwinds first first issue continued Tris first were we growth outlook spoke while of X% the cautious XXXX. for infections COVID-XX, clinical in year. arose to beginning and quarter in the versus that were trials. the was mid-February in growth X% revenue quarter renewed these we a including which Despite just this R&D many to in expressed a our currency the vaccine tissue countries in re-imposing continue decrease resolved the US. in the rollout fourth of XXXX Europe GAAP day. COVID-XX in due experience lockdowns continue to and We spikes supply saline last you
the new than as anticipated impact our as Fortunately, XXXX as QX the and quarter positive stronger revenues improved the product anticipated. our we conditions in JOTEC experienced from increased and tissue revenues impact inventory well from launches our were US unfolded less than processing
a For increased revenues of pro by XX% the first forma by of XX% full by example first last XXXX increased on the currency and year. AMDS to JOTEC revenues all XX%. in compared increased constant XXXX basis quarter quarter Nexus
on in of North On-X compared XX% In grew revenues first increased saw currency the revenues to we valve in constant first a the aortic quarter addition year. basis, quarter X% America. On-X last
competitive rather only X.X to has can the INR run X.X that valve significant a valves. patients it's FDA advantage valve reminder, X.X a As the over a from approved than that mechanically aortic In X.X. clinical to lower for On-X aortic
improved the the growth in a countries it for earnings Brazil, hospital as of has a have good the been in we've as back As Unfortunately, and us, since impact Many been in are and resurgence. there these seen US European result lockdown -- call. been And COVID you've the have market its significant a in and of COVID-XX. not all there conditions rollout US is Europe the seen US. on management COVID-XX COVID-XX has experiencing made some from improved last vaccine worst currently as progress vaccine our rollout
However, vaccine and this accelerate progress improve if forma vaccine to expect these and adoption as continue we conditions revenue the hope should in pro we regions; later rollouts that year.
the provide outlook more our QX in commentary for on later call. Ashley in -- QX will
accelerate I explained As near-term last initiatives. revenue with our key to our plan three in call, is
NEO, JOTEC of OPEN new commercialization aortic in stent the Europe. E-nside, E-nya. our stent our These products products five graft Nexus, and next-generation First, and E-vita AMDS are
into Second, America. Asia-Pacific expansion the Latin and continued
approvals PMA, an initiatives update grafts. PerClot of five these through will Third, and on in I you aortic PMA, mitral in starting includes near-term stents regulatory of review PROACT our a stent walk with major BioGlue each new markets. and China. This
used modeling First, remain device dissections the type hybrid AMDS aortic is treatment first for and we world's artery of optimistic. A very acute
XX% we of despite increase a of forma posted quarter. of in currency portion million quarter quarter, growth occurred This over first first the or revenue, during continued regional the Europe lockdowns earlier, in constant good noted $X.X a I on the basis XXXX. the pro As an through
markets. secure continue secure the for further AMDS, additional positions in particularly us pandemic dissipates we regulatory to markets in the approvals also which key expect these marketing We around authorizations increases very in world select with when to well
Europe. on Second, restrictions constant for results increase better of of well resident would if have basis these other quarter as We a $XXXXXX XXXX. the Nexus believe XX% Nexus as renewed and products posted the an been compared not first for revenues for travel of in currency to lockdowns
cases spike remain still scheduled months latest example see to continue technology. will of had result as infection in first a that for Nexus prospects For the for Nexus the several weeks upcoming the cases reschedule scheduled optimistic quarter and rates. regarding this We the we during and
our newest portfolio endovascular in Third, treat to aneurysms with stent is our thoracoabdominal E-nside device grafts.
include OPEN on is a portfolio newest our dissections currency constant when XXXX. QX our in is trunk XX% product for line This category. compared the line XXXX. grew OPEN later basis frozen Fourth, E-vita on Revenues release to which Our and this extra NEO, product we revenues to the regarding our treat this resume include to and compared QX to E-nside currency from which and Fifth, XX% of E-vita aneurysms basis E-nya, elephant of XXXX. in constant a grew market aortic NEO Plus E-vita product expect design arch. of OPEN
these for well these expect as to and demand continues. adoption vaccinations products vaccine accelerates, We five the build as products as for market adoption
expect resulting we our addition JOTEC selling supplier. improved to and a source internal second efforts from from In of own the onboarding benefit inventory,
regulatory as well as America, existing in of to products initiative, Moving these approvals for dividends to, our expansion and International our new efforts next Latin footprint These despite expansions in pandemic. Asia beginning commercial the pay are Pacific through regions.
our region Asia that, and is subsides XX% America. in anticipate growth Pacific on the of and COVID-XX Brazil. XXXX. Unfortunately, accelerate in constant Asia America, pro these quarter Pacific in a business as in authorizations basis we that regions, to pandemic the severely to revenues currency in and continues gain will impacted disproportionately both first Brazil forma in of in both by XXXX, weighted Latin marketing Latin Our first quarter increased We be additional the compared
be PMAs approval well for should as regulatory XXXX China PerClot. revenue approved, near-term initiative, this is approvals to mitral, is in the to for That FDA and PROACT expect second help half XXXX. PerClot the major continuing pursue specifically, for as first PMA Our BioGlue. third gaining in initiative submitting markets. On if we accelerate More three of program in the
manufacturing for multiple We large-scale as indications will laparoscopic capabilities. be across submitting for well specialties both, open as surgery and
are We PMA submit the on QX track in to FDA, our to XXXX.
implemented mid-XXXX, On-X in the regulatory submit Second, approval On-X valve. valves. PMA for is If will to mitral similar lower label to Coumadin, On-X we our approved label expect compared the our for of be lower valve with to maintained valve, new to patients label INR other with doses for mitral valves. INR be aortic This mechanical a able for our is on mitral patients this the for
enable to X.X after current This to rate valve for heart to patients. from an the gains Coumadin market be benefits the On-X And clinical lead Coumadin mechanical X.X. of for label the with share INR our will we'll market in INR this for us example, valve take For believe to that with our will aortic valve. mitral care similar mitral experienced to of share X.X. from market, levels, we've standard We X.X is significant approval a significant going
testing. Third, that we Chinese receive China the XXXX. This relates testing in for additional to BioGlue for equivalent request to approval approval our unlikely recently can requested is as for has in it during NMPA BioGlue in additional regulatory it that view, makes China, require may which FDA additional data the the
does near-term delay our on And we opportunity, described continue This accelerating growth view, as provide when to potential discussions clarity. the our meaningfully update We NMPA. have our we'll have approval timeline, earlier. impact in further with an I revenue not
continue we clinical are addition In good AMDS. start key U.S. in this in are to also currently ones These progress PROACT on U.S. to trials XXA, Nexus that the with are three clinical initiatives, our which mid-term later progress for products year. pipeline expect trials to make our on we and these very trials
our We trial. continue the progress enrollment in to XXA PROACT on significant make
age its the over to have Despite sites trial enrolling share approval, and in the Feedback we from early study. achieve market under be such become on enrollment, the currently FDA participating in On-X maintained XX. Eliquis XX we surgeons randomized the obtain and aortic XX can patients aortic can late warfarin. valve the of participating if qualified pandemic approval We prospective and patients believe meets assuming valve sites endpoints, the XXX trial the, by actively market headwinds Our in trial we in XXXX the still very aortic safely an currently determine will with valve XXXX. remains successfully patients If believe, patients versus and effectively clinical leader positive. we and beginning On-X the are
In addition Nexus our great progress known IDE the on partner, as trial XXA making U.S. device. its to Endospan that Triomphe. is PROACT And is trial for trial the
track recently With call FDA approvals IDE, our billion on clinical $X trial as for, to on give device year-end. we for anticipate these company we total the Nexus mid-XXXX, put market time. over acquired submitted I'll we AMDS AMDS which which our and begin that at trials now If early in Ashley. expect, Finally, our if will AMDS turn additional by would are then XXXX by the an proceed late, us in to PROACT track addressable that, submit XXA, to XXXX,