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dc.rights.licenseCC-BY-NC-ND
dc.contributor.advisorPinna, Luigi
dc.contributor.authorde la Puebla Benito, Héctor
dc.date.accessioned2023-09-06T10:09:30Z
dc.date.available2023-09-06T10:09:30Z
dc.date.issued2023
dc.identifier.urihttps://studenttheses.uu.nl/handle/20.500.12932/45061
dc.description.abstractThis review provides an understanding of the OTC landscape, assessing current incidence among patients and regions, reviewing available treatments, and identifying potential avenues for innovative interventions such as gene therapies. Simultaneously, the business plan deepens a comparative analysis, examining numerous biotechnology companies currently developing gene therapies for OTC treatment. The focus will be primarily on identifying the nature of these novel therapies and making a detailed comparison with the technology proposed by NanoRare. This assessment will not only highlight NanoRare's theoretical technical superiority, but also determine its prospective competitive position within the OTC gene therapy landscape. The business plan includes a strategic evaluation of NanoRare, to capture future valuable partners and potential investors interested in this project. This analysis intertwines the business and technological aspects of the proposed therapy, aligning them with the initial steps that could translate into a clinical trial, if all proceeds as expected.
dc.description.sponsorshipUtrecht University
dc.language.isoEN
dc.subjectThe following business plan presents an investment opportunity for potential investors in NanoCell’s groundbreaking work on Ornithine Transcarbamylase deficiency (OTC), an ultra-rare metabolic disorder. Our focus is on creating an independent, separately funded and managed entity, called NanoRare, which leverages NanoCell’s advanced gene therapy for the treatment of OTC.
dc.titleSpinning off for success: creating a comprehensive plan for NanoCell’s orphan drug branch
dc.type.contentMaster Thesis
dc.rights.accessrightsOpen Access
dc.subject.courseuuScience and Business Management
dc.thesis.id23813


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