to are Kevin. data Thank all year. and programs, said, manufacturing, quarter, activities. in like progress And ZIOPHARM clinical continued in next Kevin to This across development R&D make us the we have all of at past execution you generating our committed
me [inaudible XX:XX:XX] progress that have manufacturing Let by Houston, we facility Texas. highlighting the start made in
second recently validation completed facility, the the well quarter CPU. process built of have process own?CGMP? clinical qualification as the opening we We and the CPU. in as Commissioning safety and our and in engineering of completed ramp are unit production were
patient We we patients are library capability TCR-T of X/X our committed in a expect in the XXXX. first in support Phase dosing operationalized, dosing third the similar the to begin half to study first of Once to having manufacturing XXXX. half operational
neoantigen. them Cancer library duct screening will a are As TCR -T that that basket autologous pancreatic, Kevin T and being library. study will TCR month, actively the trial matching using ovarian Sales enrolled across Last Sleeping lung, express our study screening endometrial, our MD is engineered on indications; bile patients the colorectal the cells, fuse mentioned, on based evaluate actually service against that in Beauty open Patients are being study to trial levels. XX:XX:XX] be reactive it identify with that we with Technology. X-X tumor gives -antigen we are Phase and available neo library patients patients then and Research bearing optimal X-solid X at Transco And We our portion that Anderson treatment sectors The rapidly Center, itself on our cancers. TCR-T and as our clinical to is us design recommended approach patient's translate [inaudible believe will meaningful or effectively, and study that much indications. such the trial, Phase profile us to therapies seek of evaluate of X engine adaptive tumor as our multiple develop genetic first will the cost forward, advancing to finding progress. TCR-T the Phase dose dose, allow an dose agnostic we on to one more one and cancer This Development in move the registrational quickly of into X opportunity to across the our
pre an As of you may year, ACR recall, multiple specificity data our in on at frequent shared demonstrated with to On of targeting, recurrence, our unique with the of [inaudible these Immunotherapy program. TCR-T at strong will update Society HLA exciting annual These substitution [inaudible the data TCRs this science the Xth a earlier beyond TCRs. -clinical we will Meeting, we CT, provide XXXX Saturday, Cancer, conference on XX:XX:XX]. further Annual XX:XX:XX]
TCR bio On platform utility up we upcoming for turn the we this and file and Furthermore, validate to population owned tributary the and include that in Finally, further innovative TCR-T resources, IND over TCRs to like are to are financial internal targets including Kevin? back developed cellular subject, to generate results months validate patient for exclusivity applicable to TCR-T informatics, into to continuing Kevin, an now immunology, library the our plan genomics, expand next qualify round trials. to call strategy, have go-forward few would to library. by with TCR to the the our I us. new we review and an potential quarter. our