Dr. Harry Stylli
in made generating for quarter, our the programs. core business. especially all our business both QX innovation made and We revenue with thank Thank joining during us progress revenue we you fourth XXXX, this In with stabilizing pipeline and our progress Robert, significant afternoon.
regional contracts. are to in by payors We addition details disciplined in whilst managing approach NIPT. saw of through during payors customer reduction XXXX Further, status the and maintaining new a growth controls lay in our later and our contribution in-network commercial in we R&D and strengthen the Eric, programs. discussions These call. additional the our in-network adding acquisition CFO, grow are a more to expansion and covering improvements advanced continue which revenue cycle beyond. combination foundation maintained ASPs, commercial to resourcing for In risk factors witness operating national to sustained cost will will with beginning large to average and that force continue for expenses strong helping remaining provide we appropriate our key quarter government our and of
gross and $XXX offering During quarter, million issuance concurrent from a proceeds we the secondary of December XXXX raised notes. convertible equity in
implemented primarily now private proceeds the business pace. a accelerated progressing molecular core is placement We quarter during this including in and our evidence to addition and strengthen revenue in XXXX turnover, pipeline, COVID-XX We our management of In tests, two customer business raised were at to to that our our firms million to XX,XXX stabilizing, process. extend due tests, healthcare-focused increasing $XX QX, gross positively XX,XXX changes from reported which core investment and engagement we with focus beyond to able to it XXXX innovation see investor allows tests. that pipeline. view an our core were billing and cycle into XX,XXX we us and investor especially the was molecular leading testing In continued innovation witness fourth quarter, we drawn in our
beginning recently are significant to of to contrast, the attrition weaken. continues to now we to Separately, further losses with we’re remaining as ASP share new lives coverage quarter XXXX, and payors. reimburse an further state our And status first due to average ‘XX, contracts efforts with during its the increasing Humana, in expansion programs As further portfolio for account I’m improve quarter, from gradually our These of with as Progenity in-network and commercial additional headwind payors. Several lives of productivity risk. hopeful multiple begin By large regional payors, Medicaid payors we risk with will account new for with in-network in add attrition. secure to advancing number increased we to have continue accounts help new to covered lead to a a like should business pleased presence. more which more approach the end expect revenue NIPT offset We average that achieve well that commercial to fourth covered can we’re changes and significant X of aforementioned product as our Centene due offering the the commercial including of also NIPT. access million key significantly success. begun lives our
many average a As payors currently risk, medical it’s shift their have that most a indicated result, and policies. cover of in our permanent
rising our represents NIPT and significant growing a expect as important will aspect of revenue ASP for an average products it that risk a our make We contribution mix. to
coming our payor and early to better improved to align reminder, converted cost As We implemented approximately that And medical also patient carrier screening will transparency drive this nationally in book coverage, program revenue business. of XX% provides we the believe testing payor responsibility further testing in a aligned and patient’s which estimate result business In process. has the we in menu. revenue January, the expand a already this ASP have menu of expanded September, quarters with our in our we screening carrier policy to helped
January. changes product contribution market over experience the to trajectory the and with our quarters. channel coming across growth ASP United the from QX from our serve from show our significant expect our COVID-XX testing physicians, in and To did confident realizing that launched we impact as continue storms business in a nationally begin We NIPT patients establish the for remain will transient stabilize Taxes, we States. over growth carrier We us a volume recent We testing and revenue to within in XXXX ‘XX, winter and major these our benefits eastern and lines. QX
core and our both health is molecular helpful to by volumes. margins our testing business women’s COVID-XX remains far testing priority, While
planning the we maximize while purposes, efforts to continue demand to For our dynamics we’ll view as changing testing opportunity, COVID-XX and to transient testing opportunity. aiming to the adjust respond a accordingly rapidly
explicit our our ongoing that working ‘XX. generating diligently matters. success, and respect demonstrate contributor strong expect A more business quick are we progress litigation to to and We to positive in become with a is as note to this the revenue
believe disclosures expect and going defend and refer across and vigorously critical milestones our innovation-driven, position, our to Progenity continue is than to regard this pipeline programs. have QX, to we risk-reducing our achieved development to our on unfounded be in and this XX-K. year in While detail we call to not we’re throughout
we test, of a During in preeclampsia for primarily rule-out now intended Preecludia. is and in preeclampsia, key physicians verification complex quarter of OB/GYN our a progress test milestone rule fourth achieving the in algorithmic MFM by made with syndrome, symptomatic analysis in out multi-biomarker LDT our use patients. a The analytical the to and test, branded XXXX, significant field by development efforts clinical for
XXXX platform Annual clinical a recently verification late-breaking and with ACOG the accepted May. how an study We in our Scientific and and as performing, from our are PRO-XXX at abstract Virtual abstract Meeting assay data was pleased Clinical are with
We initiated have out which study, sample testing PRO-XXX, read for also expected validation mid-year. clinical to a is
Day During Preeclampsia Virtual the R&D fourth quarter, event. we held a
provided as well verification we data, preeclampsia. in event, clinical patient analytical understanding additional and current physicians managing from as The the and event shared unmet this groups. about During insights and perspectives needs advocacy
how by reducing pregnancies of other can unnecessary test and help the words, pre-term deliveries. be Precludia has outcomes prolonged, potential will safely We add to also provided clinical color pregnancy enhance care. on value quality the test that our improve the identifying to In
and We PRO-XXX population our systems, operational The prevalidation cohort, our from heterogeneity will in challenge selected samples of patient further further study the of analyzing expand are define and a processing understanding of randomly PRO-XXX population. our study. production from the subset target readiness our sub set currently upon broader the the the of prevalidation samples
test would for third preeclampsia U.S. clinical validation, and the successful Assuming first rule-out patients of trimester their Precludia pregnancy. be in only symptomatic the in
their As using a payors opportunity, that and realize and global our future. testing. in Precludia of of to More And economic also to research proposition. how a of better party completed is potential impact reminder, the findings, come intend to with value we value recently the commercial third were understand disease we Precludia on the characterize the the a encouraged by future. the in the would We burden very indicating understanding they
will targeted a we Precludia of half and diligently These force plans marketing for and second ‘XX. is for sales physician into including preparing launch team of accelerate commercial increase experience as Our campaigns. activities in training XXXX, the program, the move
detection our through platform. single-molecule Moving
continue to X. the We test generation the on NIPT with Innatal development next platform and its progress first make of assay
sequencing. we in dose detection integration time This ACOG’s measurable allow reduce of This across fraction. to thousands faster in response assay recent by multiplex Innatal initial a single-molecule resulting NIPT equivalent that and had in essential NIPT benchmarking. of opinion, As has to capability fraction performance COGS given We is fetal direct fetal achieve the tens performance announced and high XX%, target fourth a quantify quarter to critical, test. especially potential the highlighting the believe reminder, turnaround we to achieved achievement X a need specificity probes, up to for enabled
fuel features, X -- market. new to us usher the Innatal our With opportunities new a for growth in to these NIPT in is expected
NIPT, the genomic for projects, The be with in near and will high the single-molecule and non-RNA as several platform cost. low biomarkers our to solutions, to addition has detection future. epigenomic protein pipeline detect additional In including sensitivity suitable such opportunities platform oncology potential
to Precision Moving Medicine. GI
advance advance treat targeted other which a study ulcerative capsules, the and ulcerative in ileocecal Crohn’s DDS accurately on and will milestones update to expect the data believe cohorts. us key to device and to we and fully the key time, tolerability biomolecules single-dose disease. canine treatment in volunteers. a showing of where will safety We our autonomous half pathway distribution preclinical or year. XXX(b)(X) investigate for clinical first build of the application locate initiate the has this how orally of devices drug gastrointestinal will also The colitis, now OBDS are the autonomous autonomous date. biotherapeutic, we we done the of clinical OBDS, initiation lead to the junction The of to inhibitor a well also we This program, of the started performance ability to GI-related available. PIL solution evaluated delivered deliver of for second an are both continue a clinical capsule also DDS the key proprietary important the for fully in clinical which the The candidates, DDS Dx preclinical validation, drug three and our track transform formulation second programs behavior delivery assay to significant study separate delivery DDS its continue in announced in of autonomous and study DDS, normal payload that tract systemic a the site In well diseases. platform combination enable colon, program, vivo delivery SIBO advance study a in and system, payload clinical manufactured colitis using the the The will and a We oral adalimumab, milestone be pipeline recently study and dosing and Results Company our the be the with for the on under that JAK the you devices biotherapeutic studies, fully validate used using scintigraphic mechanism drug on a as expected This into with contract. monoclonal with this model. represent the evaluating have in in In to our year. will collect a the has Gamma our therapeutics, to tofacitinib DDS the next successful, GI the orally. healthy first using testing will potential to pilot of biotherapeutics we first study a ongoing with technology advanced, for established to are used scintigraphy shortly, If fully via the radioisotopes. saline the of a characterization. will quarter be of localization upon includes promising method of as initially study
the first the the was are Dx interview, recovery, Rao that pathologies, those reminder, without SIBO. visits XXX range a perform the of expert, need of As being patients. a million and with signs has gold Satish be PIL of a the recent GI-related standard assays variety resembling symptoms PIL Dr. the SIBO bacterial fluorescence can Dx SIBO. SIBO In suspected overgrowth evaluating potential indication a new capsule over for annual with patient There intestinal communicated based for to small for
Our last aspiration, and assay endoscopic October. to followed for conference quantifying by bacteria award small compared bowel received favorably the ACG at the section microbiology
Our analysis the systems. location for the the for both RSS a second predetermined this is and is benchtop to preserved omic recovered capsule designed from is recover discovery RSS RSS study year. by well. two fully GI drawn first same clinical sampling in diagnostics program based -- on Initiation from samples the of continues cellular on to microbial, autonomous and will the be of locations can the track of tract. us The known extracted quarter for from Once and enable range progress the with devices samples
We we the I’ll now with partners continue for turn front, With data discussion on to of to our over financial additional be potential especially we fourth call the our that, medicine generate of advance results and a with actively our expect quarter d’Esparbes, precision Eric XXXX. devices. that autonomous pipeline pharrm for as engaged as developments