key a exciting XX.X%, milestone be with double more mega sales performance Paul. another to stellar More change quarter in high double be to a proved -- higher last across delivered very driven brand €X.X growth our of the lives. in than €X.X to for as all and the quarter Care markets. just fourth for regions. period by full the to a a as immunology The sales was Libtayo year indeed billion of our quarter validates once you, franchises respective transformative for truly our patients’ brand and minute. that execute continued is franchise our Care up about Thank sales remarkable mainly It in of emerge medicines by in of on digit business and Specialty quarter. billion Sanofi largest the milestone execution oncology and the our growth mentioned Dupixent growth with and leader Specialty priorities Paul commitment Double Sarclisa digit innovative This digit in their of the in earlier, launch by unit again business
in to trajectory despite a this to €X year, on of exceed product decline oncology the sales are for we Europe. ahead, generic due billion continued Jevtana competition the in in Looking
disease sales, status Pompe Gaucher strong by demand blockbuster billion franchise Notably, exceptionally XXXX quarter fourth Fabry Pompe, in franchises. our driven up business than primarily in €X X.X%, sales. more higher reached and global across rare totaling the reported Our
great next making launched We U.S. progress of recently for ERT our the are Nexviazyme, generation in disease. Pompe uptake
Nexviazyme working standard We as global in November the in obtained Japan and are establishing next markets. of marketing have on care in approval We actively there. launched
continued potential when in Growth mainly of In of addition, number driven to forward and approval in approvals to industrial quarter XXXX was to the sales where in Cablivi, toward grew sales the of quarter which we blockers demand performance the from blood were disorders product, in to Alprolix franchise due EMA, a Sobi. US. excluding lower the work and due by continue look Europe fourth a grew franchise X.X% of in High sales competitor higher temporary the sales and fourth shortage the Kevzara, additional IL-X for of because neurology tocilizumab. a and mainly of immunology launches to receptor Europe global
result, a remain in expect partially was and we patients by is coming sales arthritis Kevzara, the in the demand quarter. declines of which to indicated of strong Kevzara for rheumatoid Strong for Aubagio months. upset with growth As the anticipated Lemtrada
driven of continue another moving that strong in billion outstanding incremental delivered added billion it alone, year in growth we just by Now U.S. than one ex-U.S. of to believe Sanofi’s number the quarter-after-quarter €X sales performance growth this beginning slide driver. consistent are now brand. journey and to the Dupixent for in Last mega the top-line, Annualizing Dupixent at making markets. €X.X year XXXX, XX. at we more sales, to of
and due in last populations. to deductible the demand, have to two remind U.S. Over years, consistent like indications commonly to strong is contributors younger new patient growth the been QX expansion of that, you the key patient the patient growth reset. in impacted QX the of I’d approval the
AD received growing for the unlock six than in AD China significant underlying more However, adult the have strongly line this our focused been their and among market. coming At European new in China, to to-date. consistent, Commission esophagitis. opinion than expectations, new years can Dupixent’s Dupixent patients a competitive listing, believe in therapy pulmonologists adolescent reflected with clinical come Europe the eosinophilic future come which specialist treated treatment the growth growth submissions Outside in have We and authorities in awareness are allergists, reinforces XXX the full to one Japan. Dupixent. becoming we time, after use biologic with which and restricted by the positive in milestones concerns, each the the years six call indications U.S. early by the in patients The has in progressing our patient rapid on, delay younger Dupixent’s resulted have continues decision options to market balancing line and first major NRDL AD. as regulatory raise as mean include at growth, some old, including bolstered can milligram In for and to old, is and in delivering including sustained as label. safety help best-in-disease efficacy. in strong CHMP Dupixent entrants the with we further believe a our of our market approvals the newly-prescribed opportunity in advancing proven cases, to in XX,XXX efficacy We potential we and U.S., In AD represent rapidly position competition was asthma, by according same a In improving access leadership, children demand some extended with young which Recent further This therapies, systemic long-term plans. of opportunity line ENTs. on second months. our launch dermatitis is with atopic final China U.S. profile, our the strengthens a remain dose, as expected dermatologists, entrants number specifically, population. we quarter-over-quarter just
as next also Dupixent about These briefly improvements in X. data confirm I prurigo pivotal topical yet were The data PRIME On patients drivers the are the two specific XX, in not indication the disease, for inadequately that lesions type benefit central therapies approved. skin Phase are and significant demonstrate which X data the in Dupixent, discuss if trials, those of IL-X targeting advisable. my slide recent therapies will controlled of potential slide. itch or the of appearance PRIME is also points for with has impressively another We IL-XX shown consistent whom in on who the two this and and confirming adding readout readouts nodularis, excited data on inflammation benefit charts across pivotal
PRIME from were the and X studies of PRIME already profile Importantly data approved in consistent well-established the with safety indications. Dupixent,
therapies. unmet high given very approved in are about lack We systemic opportunity of the excited prurigo need the and nodularis,
to are We begin of the on-track this to in first submissions half year. regulatory agencies
highlight XXXX. and no opportunities ultra of to commitment our slide or new launch to innovative there and in the bring are Specialty where exemplify Moving diseases, to two available. our sometimes fewer options market Both treatments products Care, under underserved like approved to treatment XX, addressing I’d rare
expecting is first begin plan to On CAD, the rare the European and in business developed planned the with or beginning tomorrow, key year, our our U.S. sutimlimab treatment we for are in markets launching left Sutimlimab to approval has operations. slide, side this obtain February launches for of the eagerly A disorders in product existing of blood as Japan the rollout through later of is the XXXX. and Xth. been PDUFA FDA agglutinin cold date
olipudase and basis our underscores rare quality clinical manifestations for deficiency, pediatric olipudase demonstrated rare and alfa approved, acid right has and of ASCEND-Peds unwavering life from a to the launch for separate and olipudase be slide, innovative the adult positive patients. disease two therapy that the the in olipudase for results for filings. patient’s and patients death. the the X commitment trials families evaluating delivering alfa living the upcoming non-CNS their as ASMD, Once regulatory side sphingomyelinase On of ASCEND risk premature of pediatric or disease will adult also with program The increases trial development clinical first community. only therapies served Data the and robs of for a in patients Phase of
our safety has efa, engineered our pending A the is to Factor most product combination levels with has weekly Efa week, currently maintain for efa and protection levels dose. The Considering of Phase treatment activity with weekly with patients, for slide all designed high to levels, normal patients. to potential therapies, the choice, profile the at factor practice revolutionize line than providing for much VIII of uniquely physical significantly dosing, in near completion hemophilia therapy XX, of quality therapeutic low profile the activity, of X of for enjoy improving patients ongoing levels factor treatment the burden therapies. other factor life longer factor coupled winning helping sustained the once marketed hemophilia normal trial. potential a successful a a of factor aims at of A unmatched with replacement factor convenience Turning become
a factor once high patients therapy commercial global to billion see class and Sanofi expect potential for market, With capture the the U.S. uptake we rapid significant share Japan, territories, opportunity of $X and approved. factor addressing already a on
profile also We the that a converting of treatment. portion competitive be to patient unlocking safe believe against population non-factor treatments, by efa’s non-factor factor opportunities would additional
which the waiting to the forward to results we’re on you hand I looking to we still While see vaccines to are update that, the you, at QX. with Thomas the X end Phase pivotal sharing expect With of we business. over data,