the call welcome XXXX. March just to a was Frankly, month Susan. for our I Thank everyone ended to conference want XX, our over ago. held year-end quarter you, first call
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pipeline secondary our now a quick luxeptinib, of mention But just program.
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giving chance every GX the we're so formulation succeed. And to
upcoming I'll march the we catalysts as finally, And planned mention milestones key for year. our toward
second First, our this tuspetinib meeting end parameters of on development we're program. clinical in year. in U.S. quarter the FDA is study to with of and The scheduled during steps designed agreement next of is that the tuspetinib ensure Phase the I meeting the
dose plan escalation trial. in to the in present time APTIVATE dose monotherapy exploration and and the relapsed findings Congress refractory and the doublet findings around tuspetinib patients with TUS/VEN clinical findings or Second, of dosed AML the include preliminary our we in tuspetinib patients to in EHA June,
the strategies and present doublet in Third, Fourth, Hematology potential plan clinical quarter development around Hematology tuspetinib. more development and clinical we year, accelerated XXth fifth, with to to mature dataset of meeting even for December, present to around plan ESH in tus, this tuspetinib during II the an the ASH more ven a of development plan agent. School of tuspetinib Society for discuss TUS/VEN Annual monotherapy of a of hypomethylating Meeting Exposition Annual -- with future we October, and first European Phase quarter we or And of this or robust triplet maturing dataset. fourth and pilot for
hand me to dig and trial over and go to Chief tuspetinib Dr. Let Medical AML now with you. Officer, about clinical to our Bejar, it and of Raf? plans detail with the APTIVATE lines the Rafael time clinical more