grant

Biomarker Rich Clinical Trial of an Innovative Antibody Antagonist of TNFR2 in Non-Hodgkin Lymphoma Featuring Cutaneous T Cell Lymphoma (CTCL).

Organization BOSTON IMMUNE TECHNOLOGIES AND THERAPEUTICS, INC.Location WINCHESTER, UNITED STATESPosted 1 Sept 2021Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY2025AccelerationAnimal ModelAnimal Models and Related StudiesAntibodiesAvesAvianAwardBiological MarkersBirdsBlood SampleBlood SerumBlood specimenBody TissuesBostonCD 120b AntigenCD120b AntigensCancer PatientCancer TreatmentCancersCell BodyCell Communication and SignalingCell SignalingCellsClinicalClinical EvaluationClinical TestingClinical Treatment MoabClinical TrialsCollaborationsCrab-Eating MacaqueCrab-Eating MonkeyCutaneous T-cell lymphomaCyclic GMPCynomolgus MonkeyCynomolgus macaqueDevelopmentDiagnosisDoseDrug KineticsDrugsELISAEnrollmentEnzyme-Linked Immunosorbent AssayFeedbackFibroblastsFrequenciesFundingGeneral Prognostic FactorGeneralized GrowthGrowthGuanosine Cyclic MonophosphateHealthHealth ExpendituresImmuneImmunesImmuno-ChemotherapyImmunochemotherapyImmunooncologyInfiltrationInstitutionInternationalIntracellular Communication and SignalingM fascicularisM. fascicularisMacaca cynomolgusMacaca fascicularisMacaca irusMalignant CellMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMarketingMeasuresMediatingMedical centerMedicationMolecular TargetMonoclonal AntibodiesNon-Hodgkin's LymphomaNonhodgkins LymphomaPathway interactionsPatientsPersonsPharmaceutical AgentPharmaceutical PreparationsPharmaceuticalsPharmacodynamicsPharmacokineticsPharmacologic SubstancePharmacological SubstancePhasePrivatizationProductionPrognostic FactorPrognostic MarkerPrognostic/Survival FactorReceptor ProteinReceptors, Tumor Necrosis Factor, Type IIRegulatory AffairsRegulatory T-LymphocyteResistanceResistance developmentResistant developmentSBIRSafetySecureSerumSignal TransductionSignal Transduction SystemsSignalingSmall Business Innovation ResearchSmall Business Innovation Research GrantSurrogate MarkersTM-MKRTNF-R2TNF-RIITNFR p75TNFR-Fc fusion proteinTNFRSF1B ReceptorTNR-001TNT receptor fusion proteinTNTR-FcTechnologyTestingTherapeuticTimeTissue GrowthTissuesToxicologyTregTumor MarkersTumor Necrosis Factor ActivationTumor Necrosis Factor Receptor 2Tumor Necrosis Factor Receptor 75Tumor Necrosis Factor Receptor Type 2Tumor PromotionValidationadvocacy organizationsantagonismantagonistanti-cancer therapyanti-tumor effectantitumor effectbio-markersbiologic markerbiological signal transductionbiomarkerbiomarker evaluationburden of diseaseburden of illnesscGMPcGMP productioncancer cellcancer microenvironmentcancer therapycancer-directed therapychemo-immuno therapychemoimmunotherapyclinical applicabilityclinical applicationclinical testclinical validationdesigndesigningdeveloping resistancedevelopmentaldimerdisease burdendosagedrug/agentenrollenzyme linked immunoassayhealth care expenditureimmune-oncologyimmuno oncologyimmunology oncologyinnovateinnovationinnovativeinterestlong-tailed macaquemAbsmalignancymalignant lymphocytemanufacturemarker evaluationmedical expendituremodel of animalmonoclonal Absneoplasm/cancernew approachesnew drug treatmentsnew drugsnew pharmacological therapeuticnew therapeuticsnew therapynext generation therapeuticsnon-Hodgkins diseasenovelnovel approachesnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel strategiesnovel strategynovel therapeuticsnovel therapyoncoimmunologyontogenyoverexpressoverexpressionpathwaypatient responsepatient specific responsepharmaceuticalpharmacodynamic biomarkerpharmacodynamic markerpre-clinicalpreclinicalpredict responsivenesspredicting responsepreventpreventingprognostic biomarkerprognostic indicatorprognostic significancereceptorregulatory T-cellsresearch clinical testingresistantresponseresponsive patientselective expressionselectively expressedsoluble tumor necrosis factor receptorsurrogate bio-markerssurrogate biomarkerstargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmenttherapeutic outcometherapeutic targettherapy outcometrial planningtumortumor biomarkertumor microenvironmenttumor necrosis factor receptor bindingtumor specific biomarkervalidations
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Full Description

PROJECT SUMMARY
Cancer will kill over 600,000 people in the US in 2023, causing $200B+ healthcare expenditure. This is

happening despite recent advancements in therapy and the emergence of an ever-expanding array of new

therapeutics for the over 1.9M new cancer patients every year. Indeed, because of the multitude and

redundancy of mechanisms contributing to cancer growth, therapies are often ineffective. Several components

should be targeted at the same time to maximize therapy outcome. However, this is particularly hard to attain

because of 1) the striking variability among cancers and the limited number of cancer specific targets 2) the

ability of cancer cells to orchestrate a microenvironment of healthy tissue and cells around them, that promote

cancer growth and therapy resistance.

Boston Immune Technologies and Therapeutics (BITT) is developing BITR2101, able to target both cancer

cells and their microenvironment. BITR2101 is an antagonist antibody against TNFR2 – a receptor highly

expressed in cancer tissue and immune suppressive cells in the microenvironment, where it mediates pro-

survival signaling. Thanks to BITT’s proprietary antibody design platform, BITR-2101 is the first and only

antibody able to dominantly shut down TNFR2 signaling. Due to selective expression and key role of TNFR2

for a variety of cancers and tumor microenvironment cells, BITR2101 is expected to find application in the

therapy of several cancers either as a monotherapy or in combination with other treatments. BITT has already

completed extensive pre-clinical validation for BITR-2101, demonstrating potent activity in several

malignancies in state-of-the-art animal models. As part of (R44CA265510) awarded by the NCI, BITT has

completed GLP toxicology assessment in NHPs and has confirmed the possibility to obtain cGMP grade

quality for BITR2101. This has allowed to obtain IND approval for use in NHL/CTCL. In the proposed PhaseIIb

project, BITT aims at accelerating the clinical use of BITR2101 by pursuing clinical validation in NHL/CTCL

as a keystone to demonstrate BITR2101 value in cancer therapy. This will boost the capability of BITT to

attract private funds from already contacted investors to a) complete early clinical testing (up to Phase II); b)

turn the already attracted interest of pharmaceutical companies towards our therapeutic into formal

partnerships to complete later stage clinical testing (Phase III) and launch BITR2101 into international

markets; c) explore early clinical application (Phase I-II) for additional malignancies, multiplying the impact

that our therapeutic can bring to a wide variety of cancer patients.

Grant Number: 5R44CA265510-05
NIH Institute/Center: NIH

Principal Investigator: David Brooks

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