Financial Data and Key Metrics Changes - As of December 31, 2024, the company ended the year with 100.6millionincash,cashequivalents,andinvestments,adecreasefrom174.5 million at the end of 2023 [29] - Total revenue for 2024 was 138.1million,comparedto101.2 million for 2023, attributed to collaborations with BMS, Moderna, Astellas, and Regeneron [32] - Total operating expenses for 2024 were 113.1million,upfrom107.7 million in 2023, primarily due to a 5millionmilestonepaymenttoAbbVieforCX−2051[33]BusinessLineDataandKeyMetricsChanges−Theleadprogram,CX−2051,isafirst−in−classmaskedADCtargetingEPCAM,whichiscurrentlyinclinicaltrials[9]−CX−801,amaskedversionofinterferonalpha,isalsoprogressingwellinPhase1trials,withinitialdataexpectedinthesecondhalfof2025[24]MarketDataandKeyMetricsChanges−Theunmetneedincolorectalcancerissignificant,withover1.9millionnewcasesannuallyandlimitednewtreatmentsinthelasttwodecades[13]−Thecompanyisfocusingonlate−linecolorectalcancerpatientswhohavereceivedatleastthreepriorsystemictherapies,wherecurrenttreatmentoptionsareinadequate[14]CompanyStrategyandDevelopmentDirection−Thecompanyisprioritizingitsleadprograms,CX−2051andCX−801,toextenditscashrunwaytoQ22026andsupportkeyclinicalmilestones[8]−Thestrategyincludesadvancingantibodymaskingtechnologyacrossmultipletreatmentmodalities,includingTcellengagersandcytokines[7]Management′sCommentsonOperatingEnvironmentandFutureOutlook−ManagementexpressedoptimismaboutthepotentialofCX−2051andCX−801togeneratesignificantnear−termvaluecreation,withinitialclinicaldataexpectedin2025[8]−Thecompanyremainscommittedtodisciplinedcapitalallocationandresourcemanagementtoprogressitspromisingpipeline[34]OtherImportantInformation−Thecompanyachieveda5 million milestone payment in its collaboration with Astellas for the STELLUS T cell engager program [25] - The company has decided not to continue the development of CX-904 in collaboration with Amgen, focusing instead on other promising masked T cell engagers [26] Q&A Session Summary Question: Update on CX-2051 patient enrollment and data expectations - Management anticipates a meaningful update on CX-2051, including initial safety profile characterization and potential antitumor activity data [41][42] Question: Timing for CX-801 and KEYTRUDA combination therapy - The initiation of the KEYTRUDA combination is expected in the second half of 2025, likely before data presentation [45] Question: Therapeutically active doses in CX-2051 trial - A significant number of patients will be treated with doses predicted to be within the therapeutic active range by the time data is shared [51] Question: Differential activity based on KRAS status or liver metastases - There is no obvious biology suggesting a connection between KRAS status or liver metastases and EPCAM expression; the study is enrolling a broad patient population [55] Question: Expression levels of EPCAM in colorectal cancer - EPCAM is highly expressed in colorectal cancer, and the clinical results are expected to validate this [61] Question: Focus on colorectal cancer for CX-2051 - The focus on colorectal cancer is due to high and consistent EPCAM expression, significant unmet need, and the drug's design being optimized for this indication [70][72]