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dc.contributor.authorAbouarab, Bechara
dc.contributor.authorBazarian, Christian
dc.contributor.authorBen Chaouch, Zied
dc.contributor.authorLo, Andrew W.
dc.contributor.authorMourenza Gonzalez, Guillermo
dc.contributor.authorNovak, Richard
dc.contributor.authorVigneault, Frederic
dc.date.accessioned2023-09-27T18:34:47Z
dc.date.available2023-09-27T18:34:47Z
dc.date.issued2023-09-12
dc.identifier.urihttps://hdl.handle.net/1721.1/152279
dc.description.abstractAbstract Background We consider two key challenges that early-stage biotechnology firms face in developing a sustainable financing strategy and a sustainable business model: developing a valuation model for drug compounds, and choosing an appropriate operating model and corporate structure. We use the specific example of Unravel Biosciences—a therapeutics platform company that identifies novel drug targets through off-target mechanisms of existing drugs and then develops optimized new molecules—throughout the paper and explore a specific scenario of drug repurposing for rare genetic diseases. Results The first challenge consists of producing a realistic financial valuation of a potential rare disease repurposed drug compound, in this case targeting Rett syndrome. More generally, we develop a framework to value a portfolio of pairwise correlated rare disease compounds in early-stage development and quantify its risk profile. We estimate the probability of a negative return to be $$80.8\%$$ 80.8 % for a single compound and $$56.1\%$$ 56.1 % for a portfolio of 8 drugs. The probability of selling the project at a loss decreases from $$79.2\%$$ 79.2 % (phase 3) for a single compound to $$55.4\%$$ 55.4 % (phase 3) for the 8-drug portfolio. For the second challenge, we find that the choice of operating model and corporate structure is crucial for early-stage biotech startups and illustrate this point with three concrete examples. Conclusions Repurposing existing compounds offers important advantages that could help early-stage biotech startups better align their business and financing issues with their scientific and medical objectives, enter a space that is not occupied by large pharmaceutical companies, and accelerate the validation of their drug development platform.en_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofhttps://doi.org/10.1186/s13023-023-02753-yen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMed Centralen_US
dc.titleFinancing repurposed drugs for rare diseases: a case study of Unravel Biosciencesen_US
dc.typeArticleen_US
dc.identifier.citationOrphanet Journal of Rare Diseases. 2023 Sep 12;18(1):287en_US
dc.contributor.departmentSloan School of Management
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
dc.contributor.departmentSloan School of Management. Laboratory for Financial Engineering
dc.identifier.mitlicensePUBLISHER_CC
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-09-17T03:10:32Z
dc.language.rfc3066en
dc.rights.holderInstitut National de la Santé et de la Recherche Médicale (INSERM)
dspace.date.submission2023-09-17T03:10:32Z
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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