grant

Engineered Biotherapeutic Agent for Treatment of Post-Traumatic Osteoarthritis

Organization PROVIZIGEN LLCLocation NEW YORK, UNITED STATESPosted 25 Sept 2023Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY2025(TNF)-αACL ruptureACL tearAccelerationAcuteAddressAdverse ExperienceAdverse effectsAdverse eventAffectAmericanAnimal ModelAnimal Models and Related StudiesAnimalsAnterior Cruciate LigamentAnti-InflammatoriesAnti-Inflammatory AgentsAnti-inflammatoryArthralgiaArthritisArthroplastyBehaviorBiocompatible MaterialsBiodistributionBiological AgentBiological ProductsBiological Response Modifier TherapyBiological TherapyBiomaterialsCachectinCarrier ProteinsCartilageCartilage DiseasesCartilaginous TissueCircular DichroismCommon Rat StrainsDegenerative ArthritisDegenerative DisorderDegenerative polyarthritisDevelopmentDisease ProgressionDomestic RabbitDoseDrugsEngineeringExhibitsGaitGelGoalsGrowth AgentsGrowth FactorGrowth SubstancesH elementHydrogelsHydrogenIn SituInflammatoryInjectableInjuryIntra-Articular InjectionsIntraarticular InjectionsInvestigationJoint DiseasesJoint InstabilityJoint PainJoint Prosthesis ImplantationJointsLife ExpectancyMacromolecular StructureMacrophage-Derived TNFMarketingMechanicsMedicationMicellesModelingMolecular StructureMonocyte-Derived TNFOperative ProceduresOperative Surgical ProceduresOryctolagus cuniculusOsteoarthritisOsteoarthrosisOutcomePainPainfulPatientsPharmaceutical PreparationsPhasePhysiciansPhysiologicPhysiologicalPreparationPreventative carePreventative treatmentPreventionPreventive carePreventive treatmentPropertyProtein EngineeringProteinsProteins Growth FactorsPublic HealthRabbitsRabbits MammalsRatRats MammalsRattusReconstructive Surgical ProceduresReplacement ArthroplastyReproducibilityRheologySTTRSalineSaline SolutionScanning Electron MicroscopySecond LookSecond Look SurgerySmall Business Technology Transfer ResearchStructureSurgicalSurgical InterventionsSurgical ProcedureSurgical RevisionSystemTNFTNF ATNF AlphaTNF geneTNF-αTNFATNFαTemperatureTherapeuticTherapeutic EffectTimeToxic effectToxicitiesToxicologyTransport Protein GeneTransport ProteinsTransporter ProteinTraumaTraumatic ArthritisTraumatic ArthropathyTraumatic injuryTreatment CostTumor Necrosis FactorTumor Necrosis Factor-alphaWeightanterior cruciate ligament ruptureanterior cruciate ligament teararthriticarthropathicarthropathiesarthropathyarticular cartilagebiological materialbiological therapeuticbiological treatmentbiologically based therapeuticsbiologicsbiopharmaceuticalbiopharmaceutical companybiopharmaceutical industrybiotherapeutic agentbiotherapeuticsbiotherapycartilage degenerationcartilage degradationcartilage disordercartilage repairchondroprotectionchondroprotectivecommercial applicationcytokinedegenerative conditiondegenerative diseasedegenerative joint diseasedensitydevelopmentaldisabilitydrug/agentexperienceexperimental groupfirst in manfirst-in-humangenetic protein engineeringgood laboratory practicehuman diseasehypertrophic arthritisinflamed jointinjuriesjoint arthroplastyjoint damagejoint disorderjoint inflammationjoint injuryjoint replacementjoint swellingjoint traumalight scatteringmechanicmechanicalminimally invasivemodel of animalnovelpoint of carepoint of injurypost-traumatic osteoarthritispre-clinicalpre-clinical studypreclinicalpreclinical studypreparationspreservationpreventpreventingproduct developmentprotein designreconstruction surgeryreconstructive surgerysurgeryviscoelasticityweights
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Full Description

PROJECT SUMMARY/ABSTRACT
Post-traumatic osteoarthritis (PTOA) is a degenerative disease of cartilage brought on by traumatic injury to

the articular joints. Acute joint injury is followed by severe joint pain and inflammation. This results in much

more rapid degeneration of cartilage than in other forms of osteoarthritis, due to the joint instability caused by

trauma as well as the increase in proinflammatory cytokines that accelerate degeneration. PTOA affects 5.6

million Americans, with an estimated $11.79 billion associated with direct treatment costs for its treatment.

There are no approved treatments that stop or alter the progression of the disease, and complete degeneration

of the articular cartilage can necessitate joint replacement surgery. This may require surgical revision in

approximately 10 years, a particularly undesirable outcome in younger patients with longer life expectancies.

ProViZiGen has developed a novel protein-engineered injectable therapeutic hydrogel system, HydroGEN that

forms a gel when injected into the joint space and provides sustained delivery of an anti-inflammatory and

chondroprotective therapeutic molecule. Our recent preclinical investigation in a rabbit anterior cruciate

ligament (ACL) transection model has shown that immediate delivery of HydroGEN significantly prevents the

development of PTOA after joint injury and delivery 8 weeks after the point of injury has therapeutic effects

promoting endogenous cartilage repair. In this Phase I STTR, we aim to determine stability and lack of toxicity

of HydroGEN to establish functional gelation and establish safe dosing. In Aim I, we will determine the stability

and mechanics of HydroGEN by assessing the protein’s microstructure and macrostructure, as well as its

rheologic properties as a function of temperature and time to determine its functionality as an in situ gelling

injectable therapeutic. In Aim II, we will establish the lack of toxicity and selective biodistribution of HydroGEN

in a rat model of intraarticular injection. Successful completion of these aims will prepare ProViZiGen for filing a

BLA with the FDA, with large animal PTOA model investigation (Phase II) leading to first in human trials.

Grant Number: 3R41AR083738-01S1
NIH Institute/Center: NIH

Principal Investigator: Jui Chaugule

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