And Thank good you, everyone. Jeff. afternoon,
are make discovery continuing there our Within the to XX projects important are the in are our collaborative through progress phases. across portfolio. pipeline, X programs advancing currently We and clinic,
Additionally, of programs, XX includes some therapeutics some continued to number working of last five and the are over is which proprietary proprietary we of the programs group partnered portfolio our our wholly on. increase years, have which Today, owned. are
cumulative Day, Platform believe success rates ongoing we a across the growing averages. at our to very promising highlights trend the platform. of relative discussed we and of technical completed computational and improvements is programs number As that achieving published We are collaborators meaningful signals this power our industry
and As new discovery are programs able to move the programs. complete clinic, initiate into we
recently a preclinical and As in with discovery earlier into we BMS Notably, commercialization new of as program molecules with Lilly of than advance you for for entered as of the the occurs to model to an collaborations will the development, handoff target. responsible heard products. our relationship be small completion from and Takeda. Lilly clinical well Ramy, Lilly disease studies, undisclosed
sales payments, to and to is which royalties we XXth eligible $XXX in discovery, payment, are we all royalties for to eligible on receive up new sales. future milestone and In development upfront million commercial geographies. are on This receive to program the addition commercial in an
one a deprioritize to BMS Geoff As our mentioned, of decision programs. made partnered strategic
this validated on in to elected we have Given the made program progress genetically continue the invest have target, to we internally.
We be and information to about programs able more in expect share other proprietary this XXXX. to
with also BMS. of an exploring target are alternative interest mutual We
will Turning mantle clinical advanced review initial our resistant has I cell by potential already in most and to described treatment CLL our malignancies, with signs ABC-DLBCL including of programs. B-cell MALTX a wholly-owned emerged three lymphoma, and pipeline. for SLL. as the therapeutic target others Today, or relapsed
for with recommended study of the signals pharmacokinetics, SGR-XXXX of and there malignancies, evaluate evaluate and as tumors such disease. solid proprietary to that B-cell dose cohort is could the potential as on enrollment. antitumor X to inhibitors. early is open safety, emerging combination clinical in our and BCL-X pipeline, and MALTX literature our determined of is suggesting expansion planned milestone also in company. Phase This Once study escalation have is emerging activity marks is important monotherapy. from focus our therapies, SGR-XXXX the and patient the will trial we announced is This current our inhibitor, While inhibition MALTX SGR-XXXX an other dose pharmacodynamics first that Today, autoimmune BTK
evidence Data help program, uterine cancer avoid programs WeeX our underscored including concept activity the cancers. other effects need, programs proof have identifying drug-drug can ovarian and properties has from of WeeX and WeeX other high companies’ highly of importance been to that of off-target molecules that provided WeeX clinical clinical have with observed unmet from with in data selective also of with forms several Moving optimized inhibitors. interactions in
multiple already have We potent, lead pharmacodynamic activity demonstrate with selective compounds identified ADME properties. pharmacokinetic that antitumor from series desirable and are and
afford inhibitor expect potential additional We in in us a half an the combinations. the of time select using to IND are believe characterize candidate benchmark in XXXX. the continuing first the XXXX WeeX first to and now for and will advance class to development preclinical studies best our and We taking opportunity of molecules half submit
will xenograft in report repair for inhibitor we the Annual new strong next of Today, present that in and a and inhibition full SGR-XXXX AML. patients inhibitors, on care presenting our Now, vitro in models in pathway. a suggesting or forward model. lines abstracts cell damage CDCX strategy In demonstrated for to also therapeutic look venetoclax a the month. program, published XXth. DNA cell today I the antitumor at activity other poster CDCX is we CDCX December agents, of in we AML target that or refractory treating Meeting preclinical ASH our AML in American the AML announced with standard turn strong Society to We resistant shows Hematology antitumor will SGR-XXXX FLTX to relapsed the potential activity data vivo SGR-XXXX
to XXXX. progress the IND continue IND we towards summary, the programs to this of in in half also and wholly-owned advancing. regulatory of immunology study programs oncology in clearance, X program are expect second XXXX. expand Phase Subject development first to for diverse half the FDA to and is our expect a to of submit Activities initiate and portfolio In our making submission We discovery to progressing. an are our
with are generated our Ramy. creation over the are about have on forward now already opportunities pleased coming from updating the look ahead. portfolio the progress We and months. R&D value We excited value to our turn to I we will over back you it