Good morning. Ed. you, Thank
results, growth. transformation to effort the of improvements getting improvements year. a operational corporate talented and made our started to people, strong by made acknowledging Before while our start magnitude capabilities Quanterix these last the is would set and team progress with the execution The foundation testament solid continuing intense I has long-term have to future the of like drive to
our financial quarter This those in became apparent more performance. business and strides
XX% margin prior of revenue increases quarter demand, XX% our year versus Second increased lab Accelerator increased improvement. respectively. seeing and We're XX% gross to consumables with million $XX significant driven with to XX.X% sequential business, customer non-GAAP and and by strong
positively bottom corporate line impacting is Our transformation also performance. already
full be This $XXX we full million, redevelopment our in percentage to quarter, we the XXs. gross achieved cash accelerating increased margin our XXXX flow range guidance and progress year $XXX the of in revenue With a milestone. high breakeven year million to non-GAAP
range to cash less $XX this year. $XX now burn to million expect of the also in be We million estimate and
following a quarters margins. track. ago business potential on at prime We're high-quality remind scale process the of To objective strategic the technology assays maximizing delivering strong last Simoa year now our remain corporate our transformation with our we in review initiated and a and two transformation with you, the of of
modern will and These impact that at implementation progress Quanterix, efforts our further our flow. systems new newly in at which remains operations remarkable. lines. launching Work positive SKUs have processes is long-term growth cash directly The drive and our of includes scaled and team made intensity future assay kit
correlated this with This Alzheimer's phosphorylated-tau blood-based of disease. diagnostic measures tau XXX. platform our test process. presence a aid a the amyloid has disease to In Using plasma Alzheimer's the protein of been an of high-sensitivity early July, we pathology test in launched hallmark positively brain, biomarker LucentAD, in isoform protein
LucentAD with indicate or unlikely points pathology. amyloid possible cut to provides measurements
approval to quick the test scalable therapies of this recent and screening. Leqembi, we access With the first of one promising for enable disease, will Alzheimer's anticipate
attention focused infrastructure effort deploy these Alzheimer's There's tests. of building disease as and around a well and we on as education lot will global provider patient on
your were Moving bring that announcements to like two Association recent I'd events. from There the to Alzheimer's notable International Conference to attention.
diagnose recommended the Alzheimer's First, Institute National biomarkers use Alzheimer's detect for new disease. guidelines the the Association by to of and on blood Aging, were and
listed All on Simoa. available are biomarkers of the
lot This numbers Simoa blood-based those testing. expensive large high studies of our makes LucentAD invasive cost-effective Alzheimer's systems and technology and between spinal to people amyloid the methods scalable of suspected within scans. have being demonstrated such like testing analysis screen of by to PET fluid a Numerous correlation more require in measured able as with sense cognitive biomarkers
lab to in position lab, and the of Simoa in the puts global with a in biomarker listed That Any testing for guidelines along anywhere running the every order CLIA Alzheimer's help can infrastructure the scale the great globe us platform begin reach needed build our today. therapies.
possibility data Gothenburg for Simoa blood the Sweden a Second, in study Researchers demonstrating Alzheimer's home used presented a from finger prick. technology test spot to biomarkers. collected dry was biomarkers at for from from cards the for collection blood of University
blood and results a samples micro to testing showed NFL blood. not card shipped and of liters. p-tauXXX, samples correlation all including without lot GFAP. a were temperature control facility Starting We're high p-tauXXX, biomarkers drawn tested regular of for That's to tens talking
would significant as pretty incredible an the for platform and be for promise events. capabilities Although potential ultrasensitive this Simoa study, over demonstrates early our providers a collection, home as advance blood the was of patients well traditional as it a test
neurological in expect number require cascade early will will we and monitoring, And routine biomarkers disease-modifying which a most need diagnosis therapies. to of emerging of ultrasensitivity identify decade, This these blood.
with this seeing discussed, light neurofilament injury for of last As attention or NfL chain we neuro we're approval conditions. measuring quarter Tofersen increasing of biomarker the
forward study data work levels. robust foundation data set However, by This as significant age. for to reference and the a provide comprehensive between a was pediatric a go-to adults normal NfL use set Neurology, data NFL Lancet This NfL a clinical in Simoa of levels will for for step and in the a neuro and need management further Recently test produce there's blood and vary set establishes published Simo children. enabled a adolescents for measurements. conditions
Moving of patients, XX validation better clinical the for platform efforts study consideration an positive regulators. Alzheimer's quarter collaboration to of which a readout with our this done our by we diverse and important a trial, achieved prospective demographic clinical in The potential represent entire base and aimed global BioHermes foundation. had sites physicians the top XXXX-patient to line was study
to is XXX and our announce correlation with objective scans filing work between to positive our IBD was leasing PET our the This study show to both a AD for the primary FDA. support and expected supported pleased LDT new amyloid I'm achieved.
before moment Now, a to turn to I the take over call Mike, I recap. to want
Mike? accelerated performed the and the transformation work is complete because on organization focus, the understand bearing expect we Discoveries and will not platform. treat at and of that while neurological Quanterix. the test Our yet discipline next currently Quanterix' way people Simoa XX that corporate be years disease much in levels of change will gains execution of all of at we