Thank you joining BioXcel’s call for for performance thank Operator. and discuss highlights of to the everyone and business quarter XXXX. you financial first today our Welcome
in severe acute Bipolar associated orally or IGALMI, of approval an As been with develop FDA film already Therapeutics artificial transformational transformative company disorders last or you adults. or utilizing for our for by immune-oncology. is to our of has sublingual agitation II know, I treatment first year approved month BioXcel mild, intelligence medicines and approaches a company biopharmaceutical moderate dissolving It in highlighted neuroscience the the schizophrenia
and to up to for new commercial are caregivers. this option deliver gearing We launch treatment patients
and progress team preparing deployment force our made for has tremendous U.S. finalized pricing broad national access. sales for have market of Our the
commercial discuss more Matt Commercial activities will key Chief Our Officer, in Wiley detail shortly.
X.X FDA approval or with approval trials discovery drug to validates progressed treatment and IGALMI’s in for disorder-related to BioXcel’s adjunctive treatment with which patients disorders, of strong foundation with years. human including development and or an bipolar important continued under major BXCLXXX agitation, an This associated approval also MDDs. offering in other living depressive evaluation platform, AI-enabled lays just neuropsychiatric for Alzheimer’s, option schizophrenia Beyond of treatment a disorders, the first agitation from the
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of Alzheimer’s TRANQUILTY for TRANQUILITY announced well agitation treatment with trial last acute dosing advancing in disease patient Our patients program our the is first week. with X in
TRANQUILITY FDA-approved innovative with fourth an position an the per agitation to second patient with in supplemental our top next episodes quarter for rapidly the the may no XXX estimated data year. expected therapies. X there U.S., We indication option early - This designed strategy have along of NDA and year SNDA. XXX initiated line enrolment for in of despite half enroll the the or million in helping XXXX We Alzheimer’s disease-related patients effective an year franchise which treatment are for believe provide is
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We new continue expand opportunities to with including MDD indications, TRANQUILITY and these additional our programs.
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and aggressive of We which developed and promising of prostate advanced administered for business our our clinical IO clinical business we systemic immune-oncology being an forms flexibility allows expect leading activator structure of cancer innate while this treatment continue is solid BXCLXXX, tumors. of to immunity the candidate development for financial further strategic the advance for orally
either BXCLXXX February, in data our trial Following positive past Phase phenotype. in carcinoma we adenocarcinoma II with Phase with this - patients SCNC, announced II or cell combination neuroendocrine continued mCRPC Keytruda small for
second half year. cohort We expect this enrollment to XX SCNC complete in of the our patient in
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Therapeutics year. provide of the the second will updates subsidiary additional We half this in OnkosXcel about
for milestones Qatar efforts BXCLXXX cash development our strengthened our April, on we along our and such continue of IGALMI Oaktree executing extend AI-enabled of and Authority. in confident In into and with additional our key Lastly strategic company. our we our vision XXXX commercial the With financing to strategic summary, a and across ability $XXX programs. support neuroscience with realizing commercial financing our announced activities priorities. execution pleased expansion Full will are immune-oncology with our incredibly neuroscience and leading million clinical, cash we runway Capital in Investment remain position, with becoming regulatory for clinical and progress
to like call turn would will Matt I over to update. Now the commercial Matt? Wiley, a who give