Preclinical development of CM-CX1 for the treatment of ovarian clear cell and renal cell carcinomas
Preclinical development of CM-CX1 for the treatment of ovarian clear cell and renal cell carcinomas
批准号:
10323957
负责人:
Joana M Murad
金额:
$27.41万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-08 至 2022-07-31
关键词:
ARHGEF5 geneAngiogenesis InhibitorsAntibodiesAntigensBiological AssayBiological MarkersCAR T cell therapyCD19 geneCause of DeathCell Surface ProteinsCell TherapyCell surfaceCellsCessation of lifeClear cell carcinomaClear cell renal cell carcinomaClinicClinicalClinical ResearchCombination immunotherapyCoupledCryopreservationDevelopmentDiagnosisDiseaseDoseDrug Side EffectsEffectivenessEvaluationExhibitsGoalsHematologic NeoplasmsHigh PrevalenceIdeal 1Immune checkpoint inhibitorImmune systemImmunoglobulinsImmunooncologyImmunotherapyInfusion proceduresInvestigationKiller CellsLeadLegal patentLymphocyteMalignant NeoplasmsMalignant neoplasm of ovaryMaximum Tolerated DoseModalityMucin 1 proteinNewly DiagnosedNormal tissue morphologyOrganOvarianOvarian CarcinomaOvarian Clear Cell TumorPatientsPeripheral Blood Mononuclear CellPhaseProcessProductionRefractoryRenal Cell CarcinomaRenal carcinomaRetroviridaeRiskSafetyScheduleSignal TransductionSiteSolid NeoplasmSpecificityT-LymphocyteTechnology TransferTherapeuticTimeTissuesToxic effectTumor AntigensTyrosine Kinase InhibitorUnited StatesUrogenital CancerValidationVirusWorkantibody inhibitorcancer cellcancer heterogeneitycandidate markercell bankcellular targetingcheckpoint therapychemokinechemotherapychimeric antigen receptorchimeric antigen receptor T cellscytokinecytotoxicdensitydesigneffective therapyexperiencefirst-in-humangenetically modified cellsglycoprotein CX 1immunogenicimprovedimproved outcomein vivomanufacturing facilitymortalitymouse modelneoplasticneoplastic cellnovelnovel strategiesnovel therapeuticsoptimismpersonalized cancer therapyphase 1 studypre-clinicalpreclinical developmentrat KIM-1 proteinreceptor bindingside effectsuccesssurvival outcometumorurogenital tractweapons
中文摘要
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英文摘要
PROJECT SUMMARY
Cancer is one of the leading causes of death worldwide. Over the years, a number of conventional cytotoxic
approaches for neoplastic diseases has been developed. However, due to their limited effectiveness in
accordance with the heterogeneity of cancer cells, there is a constant search for therapeutic approaches with
improved outcome, such as immunotherapy that utilizes and enhances the normal capacity of the patient's
immune system. Of note, renal cell carcinoma and ovarian cancer are considered immunogenic, or “hot”
cancers, in that tumors are infiltrated with T cells. This provides optimism that the immune system can be
harnessed to be a potent and durable weapon against these cancers.
Chimeric antigen receptor (CAR) T-cell therapy represents a major advancement in personalized cancer
treatment. In this strategy, a patient's own T cells are genetically engineered to express a synthetic receptor
that binds a tumor antigen. We have developed a CAR T cell therapy, CM-CX1, designed to target a very
specific marker (TIM-1) in renal and ovarian cancers. Expression of TIM-1 in healthy tissues is limited to
absent. The goal of this Fast Track proposal is to finalize the preclinical work required for CM-CX1 filing of
an IND for first-in-human evaluation.
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