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Industry update: the latest developments in the field of therapeutic delivery, November 2021

医学 纳米技术 业务 材料科学
作者
Peter Timmins
出处
期刊:Therapeutic Delivery [Future Science Ltd]
卷期号:13 (3): 141-156 被引量:3
标识
DOI:10.4155/tde-2022-0006
摘要

Therapeutic DeliveryVol. 13, No. 3 Industry NewsIndustry update: the latest developments in the field of therapeutic delivery, November 2021Peter TimminsPeter Timmins *Author for correspondence: Tel.: +44 1484 473 102; E-mail Address: p.timmins@hud.ac.ukhttps://orcid.org/0000-0002-5840-0678Department of Pharmacy, University of Huddersfield, Queensgate, Huddersfield, HD1 3DH, UKSearch for more papers by this authorPublished Online:7 Feb 2022https://doi.org/10.4155/tde-2022-0006AboutSectionsView ArticleView Full TextPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareShare onFacebookTwitterLinkedInReddit View articleKeywords: antibody–drug conjugatecell therapiesclinical trialsCOVID-19drug deliverygene therapymergers and acquisitionsproduct approvalsrare diseasestargeted therapeuticsReferences1. Novo Nordisk to Acquire Dicerna. https://investors.dicerna.com/news-releases/news-release-details/novo-nordisk-acquire-dicernaGoogle Scholar2. Arrowhead Pharmaceuticals enters exclusive license agreement with GSK for ARO-HSD. https://ir.arrowheadpharma.com/news-releases/news-release-details/arrowhead-pharmaceuticals-enters-exclusive-license-agreement-gskGoogle Scholar3. iX Biopharma signs exclusive license agreement for Wafermine and other sublingual ketamine wafer products. www.ixbiopharma.com/wp-content/uploads/2021/11/Press-Release-Wafermine-out-licensing.pdfGoogle Scholar4. Seelos Therapeutics announces acquisition of an exclusive license of iX Biopharma's proprietary wafer-based delivery platform for sublingual ketamine. https://seelos.irpass.com/profiles/investor/NewsPrint.asp?v=6&b=2376&ID=104187&m=rl&g=1201Google Scholar5. Lim CBS, Sunderland VB, Lee YHE. Solid dosage form. US 10857097 B2 (2020).Google Scholar6. SPRAVATO® (esketamine) nasal spray. www.janssenlabels.com/package-insert/product-monograph/prescribing-information/SPRAVATO-pi.pdfGoogle Scholar7. Blueprint Medicines to expand precision therapy leadership in lung cancer with acquisition of Lengo Therapeutics. https://ir.blueprintmedicines.com/news-releases/news-release-details/blueprint-medicines-expand-precision-therapy-leadership-lungGoogle Scholar8. Dragonfly Therapeutics announces Merck Opt-In of TriNKET™ immunotherapy candidate for patients with solid tumors. www.prnewswire.com/news-releases/dragonfly-therapeutics-announces-merck-opt-in-of-trinket-immunotherapy-candidate-for-patients-with-solid-tumors-301430512.htmlGoogle Scholar9. Our Platform: triNKET™. www.dragonflytx.com/platformGoogle Scholar10. Vifor Pharma to spearhead development of vascular calcification field, through acquisition of Sanifit Therapeutics and Inositec AG. www.viforpharma.com/vifor-pharma-spearhead-development-vascular-calcification-field-through-acquisition-sanifit-therapeuticsGoogle Scholar11. Ivarsson M, Castagner B, Leroux J-C, Pasch A. Inositol derivatives for use in pathological crystallization. US Patent 10,624,909 B2 (2020).Google Scholar12. Kedalion Therapeutics secures Series B funding and announces signing of option to acquire agreement. https://kedalionthera.com/2021/11/15/kedalion-therapeutics-secures-series-b-funding-and-announces-signing-of-option-to-acquire-agreement/Google Scholar13. Kedalion Therapeutics: technology. https://kedalionthera.com/technology/Google Scholar14. U.S. Food and Drug Administration approves Vuity™ (pilocarpine HCI ophthalmic solution) 1.25%, the first and only eye drop to treat presbyopia (age-related blurry near vision). https://news.abbvie.com/news/press-releases/us-food-and-drug-administration-approves-vuity-pilocarpine-hci-ophthalmic-solution-125-first-and-only-eye-drop-to-treat-presbyopia-age-related-blurry-near-vision.htmGoogle Scholar15. Organon to Acquire Forendo Pharma. www.organon.com/news/organon-to-acquire-forendo-pharma/Google Scholar16. Aptose enters into exclusive worldwide license agreement with Hanmi Pharmaceutical for clinical-stage myeloid kinome inhibitor HM43239. www.aptose.com/news-media/press-releases/detail/214/aptose-enters-into-exclusive-worldwide-license-agreementGoogle Scholar17. Turnstone Biologics announces research collaboration with Moffitt Cancer Center to advance novel TIL immunotherapies for solid tumor indications. www.businesswire.com/news/home/20211129005249/en/Turnstone-Biologics-Announces-Research-Collaboration-with-Moffitt-Cancer-Center-to-Advance-Novel-TIL-Immunotherapies-for-Solid-Tumor-IndicationsGoogle Scholar18. Turnstone Biologics: our science. https://turnstonebio.com/#about-usGoogle Scholar19. Turnstone Biologics acquires Novel Cell Therapy Platform. www.businesswire.com/news/home/20210120005249/en/Turnstone-Biologics-Acquires-Novel-Cell-Therapy-PlatformGoogle Scholar20. Neurocrine Biosciences and Sosei Heptares announce collaboration to develop novel muscarinic receptor agonists for schizophrenia and other neuropsychiatric disorders. https://neurocrine.gcs-web.com/news-releases/news-release-details/neurocrine-biosciences-and-sosei-heptares-announce-collaborationGoogle Scholar21. BridgeBio Pharma and Helsinn Group announce strategic collaboration to co-develop and co-commercialize BridgeBio's novel GPX4 inhibitor in multiple cancer tumor types. https://bridgebio.com/news/bridgebio-pharma-and-helsinn-group-announce-strategic-collaboration-to-co-develop-and-co-commercialize-bridgebios-novel-gpx4-inhibitor-in-multiple-cancer-tumor-typesGoogle Scholar22. Gilead exercises options to three Arcus Biosciences clinical-stage programs and adds research collaboration. https://investors.arcusbio.com/investors-and-media/press-releases/press-release-details/2021/Gilead-Exercises-Options-to-Three-Arcus-Biosciences-Clinical-stage-Programs-and-Adds-Research-Collaboration/default.aspxGoogle Scholar23. Arcus Biosciences: Clinical Pipeline. https://arcusbio.com/pipeline/chart/Google Scholar24. Novome Biotechnologies and Genentech enter into a strategic collaboration to develop targets against inflammatory bowel disease. http://novomebio.com/wp-content/uploads/2021/11/Novome-and-Genentech-Enter-into-Strategic-Collaboration.pdfGoogle Scholar25. Novome Biotechnologies reports positive results from a Phase I Study of NOV-001. http://novomebio.com/wp-content/uploads/2021/11/Novome-Reports-Positive-Results-from-NOV-001-Phase-1.pdfGoogle Scholar26. Biohaven and Pfizer enter strategic collaboration for the commercialization of rimegepant outside the United States. www.pfizer.com/news/press-release/press-release-detail/biohaven-and-pfizer-enter-strategic-collaborationGoogle Scholar27. Metagenomi and Moderna establish collaboration to develop next-generation in vivo gene editing therapeutics. https://metagenomi.co/press/metagenomi-and-moderna-establish-collaboration-to-develop-next-generation-in-vivo-gene-editing-therapeutics/Google Scholar28. Metagenomi: next generation editing systems to treat disease. https://metagenomi.co/technology/Google Scholar29. Dunad Therapeutics enters strategic collaboration with Novartis. www.dunad.co.uk/post/strategic-collaboration-with-novartisGoogle Scholar30. Dunad Therapeutics: our science. www.dunad.co.uk/Google Scholar31. Clade Therapeutics raises $87 million series A financing to realize the potential of cell therapy. https://cladetx.com/2021/11/03/clade-therapeutics-raises-87-million-series-a-financing-to-realize-the-potential-of-cell-therapy-2/Google Scholar32. Blackstone Life Sciences to invest up to $250 million in Autolus Therapeutics to develop obe-cel in adult Acute Lymphoblastic Leukemia (ALL) and advance broader platform. https://autolus.gcs-web.com/news-releases/news-release-details/blackstone-life-sciences-invest-250-million-autolus-therapeuticsGoogle Scholar33. Autolus Therapeutics announces publication describing its small molecule-regulated CAR T cells. https://autolus.gcs-web.com/news-releases/news-release-details/autolus-therapeutics-announces-publication-describing-its-smallGoogle Scholar34. Hotblack A, Kokalaki EK, Palton MJ et al. Tunable control of CAR T cell activity through tetracycline mediated disruption of protein–protein interaction. Sci. 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Merck and Ridgeback announce U.S. Government to purchase 1.4 million additional courses of molnupiravir, an investigational oral antiviral medicine, for the treatment of mild-to-moderate COVID-19 in at risk adults. www.merck.com/news/merck-and-ridgeback-announce-u-s-government-to-purchase-1-4-million-additional-courses-of-molnupiravir-an-investigational-oral-antiviral-medicine-for-the-treatment-of-mild-to-moderate-covid-19-in-a/Google Scholar50. Merck and Ridgeback announce Japanese Government to purchase 1.6 million courses of molnupiravir, an investigational oral COVID-19 antiviral medicine, upon authorization or approval. www.merck.com/news/merck-and-ridgeback-announce-japanese-government-to-purchase-1-6-million-courses-of-molnupiravir-an-investigational-oral-covid-19-antiviral-medicine-upon-authorization-or-approval/Google Scholar51. Pfizer's novel COVID-19 oral antiviral treatment candidate reduced risk of hospitalization or death by 89% in interim analysis of Phase II/III EPIC-HR study. www.pfizer.com/news/press-release/press-release-detail/pfizers-novel-covid-19-oral-antiviral-treatment-candidateGoogle Scholar52. Merck and Ridgeback Biotherapeutics provide update on results from MOVe-OUT study of molnupiravir, an investigational oral antiviral medicine, in at risk adults with mild-to-moderate COVID-19. www.merck.com/news/merck-and-ridgeback-biotherapeutics-provide-update-on-results-from-move-out-study-of-molnupiravir-an-investigational-oral-antiviral-medicine-in-at-risk-adults-with-mild-to-moderate-covid-19/Google Scholar53. Pfizer seeks emergency use authorization for novel COVID-19 oral antiviral candidate. www.pfizer.com/news/press-release/press-release-detail/pfizer-seeks-emergency-use-authorization-novel-covid-19Google Scholar54. 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Aldeyra Therapeutics announces achievement of primary endpoint of ocular redness in randomized, double-masked, vehicle-controlled Phase II clinical trial in dry eye disease. https://ir.aldeyra.com/news-releases/news-release-details/aldeyra-therapeutics-announces-achievement-primary-endpointGoogle ScholarFiguresReferencesRelatedDetails Vol. 13, No. 3 Follow us on social media for the latest updates Metrics Downloaded 55 times History Received 18 January 2021 Accepted 20 January 2022 Published online 7 February 2022 Published in print March 2022 Information© 2022 Newlands PressKeywordsantibody–drug conjugatecell therapiesclinical trialsCOVID-19drug deliverygene therapymergers and acquisitionsproduct approvalsrare diseasestargeted therapeuticsFinancial & competing interests disclosureThe author is a former employee, and is a current shareholder, of Bristol-Myers Squibb, which has active research programs and marketed medicines in some of the therapeutic areas covered in this article. The author has no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.No writing assistance was utilized in the production of this manuscript.PDF download

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