Partnering
Drug Delivery Solutions
DDS Platform & Pipeline
Drug Delivery Solutions Platform and Pipeline
Nitto BioPharma (NBPI) is a clinical stage biotechnology company that offers unique drug and nucleic acid delivery solutions by designing novel biodegradable delivery vehicles with the combined ability to target specific cells and efficiently deliver a therapeutic moiety to the cells. Over the past several years, NBPI research has resulted in both lipid and polymer based drug delivery platforms.
DDS Platform Licensing
Consistent with Nitto Denko Corporation’s commitment to “Innovation for Customers” and rooted in our deep R&D efforts to develop proprietary technologies, Nitto BioPharma is leveraging our long long-standing success and expanding our business reach through licensing its proprietary Drug Delivery Solutions (DDS) platform. Nitto takes a tailored approach towards the traditional industry licensing framework with the goal to provide this enabling technology and contribute to our customer’s value creation.
Pipeline Partnering
Nitto has a pipeline of siRNA therapeutics for KRAS Cancers and fibrotic diseases that have progressed to Phase 1 and Phase 2 clinic clinical trials. Nitto is seeking to out-license and partner these clinical assets along with additional preclinical programs.
Liver siRNA Systemic (I.V.)
Liver siRNA Systemic (I.V.)
Liver mRNA Systemic (I.V.)
Liver circular RNA Systemic (I.V.)
Lung mRNA Inhalation
Lung Gene Editing Inhalation
Liver DNA Systemic (I.V.)
Workflow
Licensing & Partnering
Our in-house analytical group can perform all required testing during development. Our CDMO partners perform all required GMP testing of raw materials, intermediates and crude API including duplexes and conjugates in most cases at the same facility, allowing for rapid turnaround of results during manufacturing campaigns. These partners are experienced in GMP release and stability testing to meet regulatory requirements.
Discussion Under CDA
Signing the CDA (Confidential Disclosure Agreement)
Confirmation of requirements for LNP
Planning a feasibility study (FS) if necessary
Feasibility Study
Signing the FSA (Feasibility Study Agreement)
Conduct feasibility studies
Accrual of technical access fees
CLA Negotiation
CLA (Collaboration and Licensing Agreement) is a definitive agreement
Arrange IP and economic terms in DDS licensing
Signing the CLA
Co-Development
Execution of product development combining your API and Nitto LNP
IND enabling development activities
Upfront and milestone payments
Program Partner
Feasibility Study
Formulation Screening
Biodistribution
Safety / Tox
Success Criteria
Optimization
Process DOE
Scalability
Stability
Safety / Tox
Manufacturing Support
Method Transfer
Lipid Procurement
IND Support
FDA Submissions
Contact Business Development
To learn more about Nitto BioPharma and our proprietary Drug Delivery Solutions (DDS) and program development capabilities click below.
Contact Business DevelopmentCorporate Deck
Request Nitto BioPharma’s corporate deck that provides an overview of Nitto BioPharma and our parent company Nitto Denko Corporation. Included in the deck is an overview of Nitto BioPharma’s proprietary Drug Discovery Solutions (DDS) Platform and it’s utility for developing genetic medicines, as well as our program and clinical development capabilities.
Request Corporate Deck