afternoon, Tim. Thanks, Good everyone.
YORVIPATH as and U.S. FDA-approved in of recent the treatment adults. only hypoparathyroidism of With approval the first the
rare coming in our disease in X from data the And the with major obtained achondroplasia product successfully U.S. EU. candidate out product candidate, in and markets, for of approval weeks. has expected Ascendis TransCon X endocrinology X third CNP pivotal
achieve our nearing vision are We XXXX. of all end product X approval candidates to of the by
a attempt focus. new through to differentiated to metabolic scientific best-in-class [indiscernible] And for us higher faster to disease on our product to disease. to candidates cardiovascular globe with and TransCon clinical CT our development. new strong bring rate continue make based across [ product as for candidates difference compared product with in a and potential success ], algorithm We technology therapeutic of Our areas such with the develop meaningful enabled last highly oncology, innovation development patients combined endocrine traditional the have drug
Let us [ XXX, patients begin alone, XX, living XXX In with YORVIPATH. U.S. ] an the are hypoparathyroidism. with estimated
disease. those of the associated in-depth take FDA Please the who having the For watch serious an arranged on hypoparathyroidism haven't consequence to understanding providing seen time it. website, patient of hearing this
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expertise. levering the our preparing U.S., and [indiscernible] are for infrastructure established commercial We YORVIPATH in
sales We of team treat XX% patients U.S. are around person the in with engage X,XXX with would dedicated who expanding would medical -- hypopara XX,XXX of our reps field and physician
launch initiatives underway. rollout key patient to programs our YORVIPATH. are support of Including support to designed Other the access
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also payers have PBMs U.S. We [ started and engaging ].
expect first to pricing, with product bed responsible possible. we price annual per value XXX,XXX availability patient the of We U.S. health care U.S. system. the premier of if launched or the will XXXX in it's Consisting YORVIPATH corresponding to soon, reflecting in a the quarter with
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currently and extremely around strong rate XX%. YORVIPATH is patients with [indiscernible]
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SKYTROFA. to Moving
the blockbuster than growth our for have are to the SKYTROFA leadership product We broader largely XX,XXX year, in as completed. well first A make that in was we while and the market SKYTROFA market. sheep of more half strategy value SKYTROFA or both for label. ave assess broadened patients patients for a overall assets market simplifying expanding our proud X-year treatment include component have U.S. first the In key expanding symptoms to the to to market a set of switch as hormone
long-term the demand first short While access term, half impacted revenue. will Scott our broader will negatively to it this details. support share net in SKYTROFA more
premium value our completed. now a positioned With Xx a of as product transition net with is SKYTROFA compared around to [indiscernible]. prepatient largely markets
We the in focused now growth are aiming drive assess and overall hormone on the to demand. using data are to market new expand covers U.S. to market further Continue SKYTROFA for alone. blockbuster our reach
quarter deficiency BLA to leadership position. FDA our in the of build third the this growth submit supplement and plan to on year. to market adult in hormone We Finally,
first SKYTROFA Our expansion. label
from data in II expect Syndrome line fourth the XXXX. of top in trial quarter Turnet Phase our also We
from now extremely and result Switching fewer much about our have program in we in excited as been achondroplasia, to TransCon more approaching weeks. CNP. coming I trial the our are always the
growth in We [indiscernible] achondroplasia. address with a have of our people that that X announced candidate aim past treatment since for is living and [indiscernible] consistent develop our linear both that the years we health over our quality affect and product to life
Earlier [ X.X this saw a of after vosoritide competitive increased ] about similar year, CNP centimeter trial. XX II TransCon our months sort result for accomplish that our once-weekly velocity treatment. to Demonstrating growth annualized you Phase
addition, TransCon favorable demonstrated life the function ] first-time a ] with AX In with with also side tolerability in the [ CNP of physical quality we effect to achondroplasia, and product profile. that associated [indiscernible] of for improved placebo, of Belvin achondroplasia compared [ setting in
we trial years, to in X.X data expecting trial. II approach Now these with with [indiscernible] are in similar quarter we X [indiscernible] [indiscernible]. we our patients earlier This enrolled line The X top XX to the few that replicate hope guided. more Phase pivotal trial, can weeks, our mean and age than results next
COD We CNP II to a show [ designed [indiscernible] to Growth adding trial TransCon enrolling with group combination also start TransCon up in Phase to provide SKYTROFA ] patients in cash of continue treatment late. who could TransCon that CNP CNP for
of trial the quarter during enrollment expect quarter data fourth XX with first the to second expected We top XXXX, in of line this XXXX. in combination complete
oncology. now Turning to
Agonist combination X/X X with different We TransCon best-in-class continue I a trials believe TransCon this potential are [ TransCon resistant the to IL-X and with TLR beta/gamma the present in in X cohort pleased multiple with plan Phase chemotherapy big scenarios. the combination tried study this to progressing. our indications I'm advancing candidates, month Barcelona. tuberine product of II our from at We conference results in in later how initial IL-X plasm program from ] ESMO beta/gamma cancer award
oncology the the all Descartova parents achondroplasia. the for our With With exploration has and program obesity. In show are living able transformative. expected that the We life market of from approval ongoing areas week closing, the people TransCon innovation transform our is parents also life about patients. [ It hear Patients that of changed goal to for CNP. both. in we children data Ascendis, us as in such we opportunity with U.S. of progress ] in it's is that our tell other of that of and next YORVIPATH
an TransCon candidate. for position with sustainable We expanded continue transformative Ascendis to pipeline growth and product
Scott it now update. financial I'll a turn for to over