Thank you, Carrie.
diseases programs well program as we this continue and are We our very core all adjacent expect stages with where advancement progress of In make pipeline significant immunology, rheumatology expanding areas as in in of we our good year. portfolio. our dermatology, to across
for other will SKYRIZI our include this SKYRIZI's versus head-to-head of will We're studies Otezla. a used year from SKYRIZI. add registrational III from of III Phase competitive anticipated this supporting versus evaluating These submissions Phase which for regulatory later Phase trial Results in best-in-category studies we III disease completion studies ulcerative We'll these and with major also induction expect in STELARA our which body the In year. first its to from half nearing distinguish colitis these from ulcerative program evidence profile agents studies we'll colitis program last in our see trial SKARIZI Crohn's versus in commonly data as of further maintenance indication in is agent the the this year, expansion SKYRIZI our and psoriasis offerings. the data see comparison indications.
completion of the indication nearing also programs expansion RINVOQ. for core We're
rates for inhibitor have approved treatment remains a TNF new is approximately This market high where unmet used anticipate the regulatory demonstrated once improvement of an of Our maintenance RINVOQ important are applications RINVOQ Crohn's option Crohn's deliver in bioexperience patients XX% in remission. and will induction that approval and quarter. for endoscopic disease remission our we and studies decisions RINVOQ can III second strong be believe rates and under disease. review there long-term of Phase and and very need we the considerable response and therapies in
we've Beyond a potential several indications, inhibitor therapy. strong RINVOQ where immunology we're highly to our evidence diseases seen has the become our effective JAK that core in developing
giant in III alopecia these Phase And of begin Phase studies suppurativa, this systemic we hidradenitis program for arteritis. X Our X is plan cell and additional underway vitiligo year, lupus, already diseases, III areata. later indications, to
In their year. oncology, Phase important indications. milestones Venclexta's myelofibrosis. studies regulatory and multiple of several oncology from our support second trial in including with respective several Moving TXXX Navitoclax' we studies, navitoclax expected are where now data this Results in from patients year half the in event-driven in myeloma TRANSFORM-X and these trial clinical regulatory the for see we'll de submissions hematology and of from results expect to Venclexta the novo a portfolio, area frontline relapsed/refractory III mutation to
year. potential We epcoritamab for the to has progress, thus geographies, the believe epcoritamab believe therapy become in responses upon also has significantly development lymphoma the our relapsed/refractory Europe we malignancies. continue and major make our programs And in in far epcoritamab the the anticipate in B-cell Japan quarter we We a program, for drillable potential regulatory across Based several and epcoritamab these for clinical large approval improve that patients. U.S. the to very of demonstrated the half this on good several in deep and that second year second indications. very for options including to B-cell treatment core expanding in
Over the and on malignancies studies and II course the data as several and programs of in to Phase forward best-in-class studies, III combination with multiple very remain in CLL in providing R-CHOP become therapy frontline We MCL. XXXX, potential we updates new expect across DLBCL to including multiple Phase to B-cell look these mature. about a begin epcroritumab's a excited study
Now to in see second-line data plus pipeline. year We solid II our non-squamous Teliso-V non-small later cancer. our remain advanced cell tumor moving Phase evaluating study lung this on from track
As year a c-Met designation based and ADC, reminder, potential on the an results from has II we'll the this for later study we data therapy the see this of encouraging received support Phase to X a approval. Stage breakthrough Teliso-V, accelerated our
confirmatory Our also is c-MET in ongoing. Phase study patients overexpressed with III
these poor. Treatment who exhausted patients are patients chemotherapy, cancer options have very prognosis for immunotherapy for and targeted limited platinum-based and extremely is these therapy
ADC, more be solid tumors. the used can drive deeper broaden which c-MET inhibitor c-MET responses topoisomerase of important therapies overexpressed As also potential population, new making which cell of Teliso-V a we for the has lung good treatment option believe next-generation as therapy potent potentially such approximately cement cancer patients. as colorectal a non-squamous for with well XX% to utilizes our tumor with non-small represents range to ABBV-XXX targeted and progress as these patients gastroesophageal become the payload, We're where an tumors
from I We in see to XXXX. expect Phase our program early data
programs Phase advance see II pipeline, solid year. encouraging data we have we from studies plan the tumor begun into which this to several to in Elsewhere
ABBV-XXX activity, strong antibody, types. on showing deep anti-GARP to signals with Phase plan studies prolonged several II in responses durability. efficacy, preliminary Based Our we tumor is including this of initiate
non-small to a Phase also subset this of year based ABBV-XXX cell stage combined ADC on promising approximately is of the our cancer c-MetSo non-small non-squamous patients. into XX% optimizing PTKX will lung which c-Met cell cancer lung targets program. This our approximately advance and plan studies target early overlap results We ADCs from II and little has dose non-squamous PTKX patients and XX% ADC represents of with
FDA which fourth approval we pleased excited risk benefit disorder adjunctive or marks label an Now approval received very major approval. the We're is continue indication moving important highlights antidepressant to its patients by an strong Real as this new to treatment taking neuroscience, option Vraylar where for Vraylar treatment which depressive symptoms. are recently who with an for in have unresolved depression profile indication. but currently this for and
We DUOPA DUOPA-LIKE options. approval both ABBV-XXX, secured other In half patient the expected U.S., second improvement potential for transformative potentially remain in delivery more system, subcutaneous This a levodopa year, half also U.S. the launch system the expand anticipate disease. received it currently we approval brain therapies addressed after or also and approval reimbursement. in delivery our product deep invasive the first Parkinson's the population in Japan we delivering by in efficacy such track approach on recently PD to year for current We a of for to nonsurgical With has this as treatment with stimulation. invasive, of delivery represents less system Europe. decisions advanced subcutaneous patients a the innovative novel to through the advanced significantly carbidopa for treatment
and migraine, of a decision the new patients Europe, chronic migraine. remain a we area a is we of oral would anticipate Lipa both the approval as FDA year we And third quarter Europe, an for to it And we disease quarter approved, prevention approval available to QULIPTA approval feature in for for quarter of that only forward life oral chronic with for look In option year. chronic patients for with this preventive for for in significantly in in approved once impacts treatment this treatment patients the track as would migraine. the second this differentiating on of in This CGRP debilitating and decision an episodic in fourth migraine. the preventive as anticipate approved. quality another common with treatment patients this be If and make be atogepant
expect prominence from toxin several Phase we III in And near international portfolio help the for BOTOX U.S. X in prominent the regulatory see in where we expected jaw Phase year from expect data of aesthetics the our submit China certain masseter our results our submission and platysma data our to in novel end and for Canada. to XXXX programs to the well These study segment. for III year, pipeline, muscle Botox including this half as study muscles with lower build the including from in second in markets regulatory further of prominence, applications will as indications phase neck in
data We'll applications or end with from also our III toxin of this year Bot-AE the plan glabellar for in short-acting Phase XXXX. see for regulatory trial lines near
in numerous So XXXX. and we summary, all our in stages demonstrate anticipate progress pipeline clinical milestones and again continue regulatory to of important across significant
With to our Rob Rob? the call and turn on quarter that, comments over XXXX financial performance fourth additional our for outlook. I'll