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 the corresponding period in 2023, attributed to collaborations with BMS, Moderna, Astellas, and Regeneron [32] - Total operating expenses for 2024 were 113.1million,anincreasefrom107.7 million in 2023, primarily due to a 5millionmilestonepaymentforCX−2051[33]BusinessLineDataandKeyMetricsChanges−Theleadprogram,CX−2051,isafirst−in−classADCtargetingEPCAM,withafocusoncolorectalcancer,whichhasasignificantunmetneed[7][13]−CX−801,amaskedversionofinterferonalpha,isalsoprogressingwellinearlyclinicaltrials,withplanstoinitiatecombinationtherapywithKEYTRUDAin2025[24]MarketDataandKeyMetricsChanges−Theglobalunmetneedincolorectalcancerissignificant,withover1.9millionnewcasesannuallyandlimitednewtreatmentsemerginginthelasttwodecades[13]−Thecompanyisfocusingonlate−lineCRCpatientswhohavegenerallyreceivedatleastthreepriorsystemictherapies,indicatingahighunmetneedinthispatientpopulation[15][70]CompanyStrategyandDevelopmentDirection−Thecompanyisprioritizingitsleadprograms,CX−2051andCX−801,toextenditscashrunwaytoQ22026andsupportkeyclinicalmilestones[8][29]−Thestrategyincludesafocusonantibodymaskingtechnologyandcollaborationswithmajorpharmaceuticalcompaniestoenhanceitspipeline[7][25]Management′sCommentsonOperatingEnvironmentandFutureOutlook−ManagementexpressedoptimismabouttheinitialclinicaldataforCX−2051andCX−801expectedin2025,whichcoulddrivesignificantnear−termvaluecreation[8][28]−Thecompanyremainscommittedtodisciplinedcapitalallocationandresourcemanagementtoprogressitspromisingpipeline[34]OtherImportantInformation−Thecompanyachieveda5 million milestone in its collaboration with Astellas, indicating ongoing progress in its partnerships [31][25] - The company is not pre-selecting patients based on EPCAM expression or other disease characteristics in its Phase 1 study for CX-2051, aiming to characterize the drug across the full CRC population [15][56] Q&A Session Summary Question: Update on CX-2051 patient enrollment and data expectations - Management anticipates a meaningful update 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 the year, 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: Expectations regarding KRAS status and liver metastases - There is no obvious biology suggesting a connection between KRAS status and EPCAM expression; the study aims to enroll a broad patient population [55] Question: Expression levels of EPCAM in CRC - EPCAM is highly expressed in colorectal cancer, and the clinical results are expected to validate this [61] Question: Focus on CRC for EPCAM targeting - The focus on CRC is due to its high and consistent EPCAM expression, significant unmet need, and the drug's design being optimized for this indication [70]