grant

Rapid and Ultra-Pure mRNA Production with Next-Generation RNA Polymerases

Organization CISTERNA BIOLOGICS, INC.Location OCEANSIDE, UNITED STATESPosted 5 Jun 2025Deadline 31 May 2027
NIHUS FederalResearch GrantFY20252019-nCoV vaccineAbscissionAddressAdvanced DevelopmentAntigensBiochemicalBioinformaticsBiological AgentBiological ProductsBiotechBiotechnologyCOVID-19 vaccineCancersCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemCatalytic RNACell TherapyCelluloseClinicalCollaborationsCommunicable DiseasesCoupledCustomDNA-Dependent RNA PolymerasesDNA-Directed RNA PolymeraseDangerousnessDevelopmentDoseDouble-Stranded RNAElementsEngineeringEnvironmentEnzyme GeneEnzymesExcisionExtirpationFDA approvedFaceGene TranscriptionGenetic TranscriptionGoalsHeart VascularImmuneImmune Cell ActivationImmune responseImmunesImmunomodulationIn VitroIndustrializationIndustry StandardInfectious DiseasesInfectious DisorderInnate Immune ResponseInnate ImmunityLeadMalignant NeoplasmsMalignant TumorMarketingMessenger RNAMetabolic DiseasesMetabolic DisorderMethodsNative ImmunityNatural ImmunityNon-Polyadenylated RNANon-Specific ImmunityNonspecific ImmunityNucleotidesPb elementPharmaceutical AgentPharmaceuticalsPharmacologic SubstancePharmacological SubstancePhasePolyanhydroglucuronic AcidProcessProductionPromoter RegionsPromotor RegionsPseudouridineRNARNA ExpressionRNA Gene ProductsRNA NucleasesRNA PolymerasesRNA based therapeuticsRNA based therapyRNA chemical synthesisRNA purificationRNA replicationRNA synthesisRNA therapyRNA vaccineRNA-based vaccineRNaseReactionRecoveryRemovalRibonuclease Family ProteinRibonucleasesRibonucleic AcidRibozymesSARS-CoV-2 vaccineSARS-coronavirus-2 vaccineSBIRSafetyServicesSevere Acute Respiratory Syndrome CoV 2 vaccineSevere acute respiratory syndrome coronavirus 2 vaccineSmall Business Innovation ResearchSmall Business Innovation Research GrantSolidSurgical RemovalT7 RNA polymeraseTechnologyTexasTherapeuticTherapeutic UsesThesaurismosisTranscriptionTranscription ProcessTreatment EfficacyUniversitiesUrdUridineVaccinesValidationWorkalpha-Celluloseanaloganti-cancer immunotherapyanticancer immunotherapyaptamerbasebasesbiologicsbiopharmaceuticalbiotherapeutic agentcancer immunotherapycell based interventioncell mediated interventioncell mediated therapiescell-based therapeuticcell-based therapycellular therapeuticcellular therapychemical stabilitycirculatory systemcold temperaturecommercial scale manufacturingcoronavirus disease 2019 vaccinecoronavirus disease-19 vaccinecostcost effectivecustomsdevelopmentaldosagedsRNAfacesfacialgenetic promoter elementgenetic promoter sequenceheavy metal Pbheavy metal leadhost responseimmune activationimmune modulationimmune regulationimmune system responseimmune-based cancer therapiesimmunogenimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryimmunoresponseimmunotherapy for cancerimmunotherapy of cancerimprovedin vivoinhibitorinnovateinnovationinnovativeintervention efficacylow temperaturemRNAmRNA vaccinemRNA-based vaccinemalignancymanufacturing ramp-upmanufacturing scale-upmetabolism disordernCoV vaccinenCoV-19 vaccinenCoV19 vaccineneoplasm/cancernext generationnoveloligo (dT)oligodeoxythymidylic acidpatient responsepatient specific responsepharmaceuticalpromoterpromoter sequencepromotorresectionresponsive patientscale up batchscale up productiontherapeutic RNAtherapeutic efficacytherapy efficacyupscale manufacturingvaccine against 2019-nCovvaccine against COVID-19vaccine against SARS-CoV-2vaccine against SARS-coronavirus-2vaccine against Severe Acute Respiratory Syndrome CoV 2vaccine against Severe acute respiratory syndrome coronavirus 2vaccine candidates against SARS-CoV-2vaccine for novel coronavirusvaccines preventing COVIDvaccines to prevent COVIDvalidations
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Full Description

PROJECT SUMMARY
Cisterna Biologics is addressing critical challenges in mRNA purification for therapeutic applications by

developing a novel production and purification process. This Phase I SBIR aims to generate ultra-pure mRNA,

essential for high-dosage and frequent administration in treatments ranging from enzyme replacement to cancer

immunotherapy. Traditional in vitro transcription (IVT) methods using T7 RNA polymerase produce significant

byproducts that can trigger adverse immune responses. In collaboration with the University of Texas-Austin,

Cisterna's approach involves the development of cold-adapted (psychrophilic) RNA polymerases (RNAPs),

which maintain high activity at low temperatures and reduce byproduct formation. Additionally, Cisterna's

proprietary SPEcific Capture and Cleavage (SPECC) purification technology intends to eliminate contaminants

completely. The Phase I SBIR project will demonstrate the capability of this technology to synthesize

contaminant-free mRNA, improving safety and efficacy for therapeutic use. Initial aims include optimizing

psychrophilic RNAPs and synthetic promoters to minimize contaminants significantly, with the ultimate goal of

replacing current gold-standard purification methods. The successful completion of this phase will pave the way

for Phase II, focusing on scaling up manufacturing and validating the platform in clinical settings. As the mRNA

therapeutics market is projected to grow substantially, Cisterna plans to establish itself as a leader in high-quality

mRNA production, leveraging its technologies and potential partnerships with biotech and pharmaceutical

companies.

Grant Number: 1R41GM159477-01
NIH Institute/Center: NIH

Principal Investigator: Hari Bhaskaran

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