US 5212295A
· Cook
· 1993
[cited by applicant]
US 5521302A
· Cook
· 1996
[cited by applicant]
US 5587361A
· Cook et al.
· 1996
[cited by applicant]
US 5792615A
· Arnold, Jr. et al.
· 1998
[cited by applicant]
US 6146829A
· Cook et al.
· 2000
[cited by applicant]
US 6172209B1
· Manoharan et al.
· 2001
[cited by applicant]
US 6639022B2
· Michels et al.
· 2003
[cited by applicant]
US 6867294B1
· Sanghvi et al.
· 2005
[cited by applicant]
US 6949520B1
· Hartmann et al.
· 2005
[cited by applicant]
US RE39464E
· Cook et al.
· 2007
[cited by applicant]
US 7919472B2
· Monia et al.
· 2011
[cited by applicant]
US 7947658B2
· Aronin et al.
· 2011
[cited by applicant]
US 7951934B2
· Freier
· 2011
[cited by applicant]
US 8415465B2
· Freier
· 2013
[cited by applicant]
US 8470987B2
· Wada et al.
· 2013
[cited by applicant]
US 8481710B2
· Davidson et al.
· 2013
[cited by applicant]
US 8679750B2
· Hayden et al.
· 2014
[cited by applicant]
US 8680063B2
· Aronin et al.
· 2014
[cited by applicant]
US 8822671B2
· Shimizu et al.
· 2014
[cited by applicant]
US 8859755B2
· Wada et al.
· 2014
[cited by applicant]
US 8906873B2
· Hung et al.
· 2014
[cited by applicant]
US 8952145B2
· Freier
· 2015
[cited by applicant]
US 8987222B2
· Aronin et al.
· 2015
[cited by applicant]
US 9006198B2
· Bennett et al.
· 2015
[cited by applicant]
US 9057066B2
· Hung et al.
· 2015
[cited by applicant]
US 9260716B2
· Davidson et al.
· 2016
[cited by applicant]
US 9353372B2
· Freier
· 2016
[cited by applicant]
US 9394333B2
· Wada et al.
· 2016
[cited by applicant]
US 9476044B2
· Tuschl et al.
· 2016
[cited by applicant]
US 9598458B2
· Shimizu et al.
· 2017
[cited by applicant]
US 9605019B2
· Verdine et al.
· 2017
[cited by applicant]
US 9617547B2
· Gemba
· 2017
[cited by applicant]
US 9683236B2
· Hung et al.
· 2017
[cited by applicant]
US 9695211B2
· Wada et al.
· 2017
[cited by applicant]
US 9744183B2
· Verdine et al.
· 2017
[cited by applicant]
US 9982257B2
· Butler et al.
· 2018
[cited by applicant]
US 11634710B2
· Frank-Kamenetsky et al.
· 2023
[cited by applicant]
US 20020082227A1
· Henry
· 2002
[cited by applicant]
US 20020183502A1
· Mesmaeker et al.
· 2002
[cited by applicant]
US 20140303235A1
· Oestergaard et al.
· 2014
[cited by applicant]
US 20150292015A1
· Bennett et al.
· 2015
[cited by applicant]
US 20170130224A1
· Oestergaard et al.
· 2017
[cited by applicant]
US 20190264267A1
· Yang et al.
· 2019
[cited by applicant]
US 20200362337A1
· Dodart et al.
· 2020
[cited by applicant]
US 20220098585A1
· Brown et al.
· 2022
[cited by applicant]
US 20220145300A1
· Liu et al.
· 2022
[cited by applicant]
US 20220186217A1
· Zhang et al.
· 2022
[cited by applicant]
US 20220195429A1
· Vargeese et al.
· 2022
[cited by applicant]
US 20220307019A1
· Yokota et al.
· 2022
[cited by applicant]
US 20230136645A1
· Butler et al.
· 2023
[cited by applicant]
US 20230203087A1
· Kandasamy et al.
· 2023
[cited by applicant]
US 20230220384A1
· Monian et al.
· 2023
[cited by applicant]
US 20230295617A1
· Vargeese et al.
· 2023
[cited by applicant]
US 20230295619A1
· Maguire et al.
· 2023
[cited by applicant]
US 20230329201A1
· Yang et al.
· 2023
[cited by applicant]
US 20230392137A1
· Monian et al.
· 2023
[cited by applicant]
US 20240026358A1
· Monian et al.
· 2024
[cited by applicant]
US 20240109931A1
· Vargeese et al.
· 2024
[cited by applicant]
US 20240132894A1
· Vargeese et al.
· 2024
[cited by applicant]
US 20240175018A1
· Vargeese et al.
· 2024
[cited by applicant]
US 20240229026A1
· Butler et al.
· 2024
[cited by applicant]
US 20250051778A1
· Byrne et al.
· 2025
[cited by applicant]
EP 2873674A1
· 2015
[cited by applicant]
JP H06220083A
· 1994
[cited by applicant]
JP 2003238586A
· 2003
[cited by applicant]
JP 2011184318A
· 2011
[cited by applicant]
RU 2616283C2
· 2017
[cited by applicant]
WO WO9308296A1
· 1993
[cited by applicant]
WO WO9905160A2
· 1999
[cited by applicant]
WO WO2005014609A2
· 2005
[cited by applicant]
WO WO2005023828A1
· 2005
[cited by applicant]
WO WO2005027980A1
· 2005
[cited by applicant]
WO WO2005028494A1
· 2005
[cited by applicant]
WO WO2005070859A1
· 2005
[cited by applicant]
WO WO2005085272A1
· 2005
[cited by applicant]
WO WO2005092909A1
· 2005
[cited by applicant]
WO WO2005111057A2
· 2005
[cited by applicant]
WO WO2007131237A2
· 2007
[cited by applicant]
WO WO2007131238A2
· 2007
[cited by applicant]
WO WO2007134014A2
· 2007
[cited by applicant]
WO WO2007134181A2
· 2007
[cited by applicant]
WO WO2007136988A2
· 2007
[cited by applicant]
WO WO2007139190A1
· 2007
[cited by applicant]
WO WO2007143315A2
· 2007
[cited by applicant]
WO WO2007143316A2
· 2007
[cited by applicant]
WO WO2007143317A2
· 2007
[cited by applicant]
WO WO2007146511A2
· 2007
[cited by applicant]
WO WO2008049085A1
· 2008
[cited by applicant]
WO WO2010064146A2
· 2010
[cited by applicant]
WO WO2010091301A1
· 2010
[cited by applicant]
WO WO2011005761A1
· 2011
[cited by applicant]
WO WO2011034072A1
· 2011
[cited by applicant]
WO WO2011082281A2
· 2011
[cited by applicant]
WO WO2011108682A1
· 2011
[cited by applicant]
WO WO2012039448A1
· 2012
[cited by applicant]
WO WO2012073857A1
· 2012
[cited by applicant]
WO WO2012109395A1
· 2012
[cited by applicant]
WO WO2012145729A2
· 2012
[cited by applicant]
WO WO2013012758A1
· 2013
[cited by applicant]
WO WO2013022984A1
· 2013
[cited by applicant]
WO WO2013112053A1
· 2013
[cited by applicant]
WO WO2014010250A1
· 2014
[cited by applicant]
WO WO2014010718A1
· 2014
[cited by applicant]
WO WO2014012081A2
· 2014
[cited by applicant]
WO WO2014118267A1
· 2014
[cited by applicant]
WO WO2014121287A2
· 2014
[cited by applicant]
WO WO2014179626A2
· 2014
[cited by applicant]
WO WO2015051214A1
· 2015
[cited by applicant]
WO WO2015107425A2
· 2015
[cited by applicant]
WO WO2015108046A1
· 2015
[cited by applicant]
WO WO2015108047A1
· 2015
[cited by applicant]
WO WO2015108048A1
· 2015
[cited by applicant]
WO WO2016079181A1
· 2016
[cited by applicant]
WO WO2016096938A1
· 2016
[cited by applicant]
WO WO2016127000A1
· 2016
[cited by applicant]
WO WO2017015555A1
· 2017
[cited by applicant]
WO WO2017015575A1
· 2017
[cited by applicant]
WO WO2017062862A2
· 2017
[cited by applicant]
WO WO2017067970A1
· 2017
[cited by applicant]
WO WO2017160741A1
· 2017
[cited by applicant]
WO WO2017192664A1
· 2017
[cited by applicant]
WO WO2017192679A1
· 2017
[cited by applicant]
WO WO2017210647A1
· 2017
[cited by applicant]
WO WO2018022473A1
· 2018
[cited by applicant]
WO WO2018067973A1
· 2018
[cited by applicant]
WO WO2018098264A1
· 2018
[cited by applicant]
WO WO2018223056A1
· 2018
[cited by applicant]
WO WO2018223073A1
· 2018
[cited by applicant]
WO WO2018223081A1
· 2018
[cited by applicant]
WO WO2018237194A1
· 2018
[cited by applicant]
WO WO2019032607A1
· 2019
[cited by applicant]
WO WO2019032612A1
· 2019
[cited by applicant]
WO WO2019055951A1
· 2019
[cited by applicant]
WO WO2019075357A1
· 2019
[cited by applicant]
WO WO2019200185A1
· 2019
[cited by applicant]
WO WO2019217784A1
· 2019
[cited by applicant]
WO WO2020118246A1
· 2020
[cited by applicant]
WO WO2020160336A1
· 2020
[cited by applicant]
WO WO2020191252A1
· 2020
[cited by applicant]
WO WO2020196662A1
· 2020
[cited by applicant]
WO WO2020219981A2
· 2020
[cited by applicant]
WO WO2020219983A2
· 2020
[cited by applicant]
WO WO2020227691A2
· 2020
[cited by applicant]
WO WO2021071788A2
· 2021
[cited by applicant]
WO WO2021071858A1
· 2021
[cited by applicant]
WO WO2021178237A2
· 2021
[cited by applicant]
WO WO2021234459A2
· 2021
[cited by applicant]
WO WO2021237223A1
· 2021
[cited by applicant]
WO WO2022046667A1
· 2022
[cited by applicant]
WO WO2022046723A1
· 2022
[cited by applicant]
WO WO2022099159A1
· 2022
[cited by applicant]
WO WO2023049475A1
· 2023
[cited by applicant]
WO WO2023049477A2
· 2023
[cited by applicant]
WO WO2023075766A1
· 2023
[cited by applicant]
WO WO2023076352A2
· 2023
[cited by applicant]
WO WO2023154528A1
· 2023
[cited by applicant]
WO WO2023168014A2
· 2023
[cited by applicant]
WO WO2023201095A2
· 2023
[cited by applicant]
WO WO2023220440A1
· 2023
[cited by applicant]
WO WO2024035946A1
· 2024
[cited by applicant]
WO WO2025030155A1
· 2025
[cited by applicant]
U.S. Appl. No. 17/605,998, filed Oct. 22, 2021, Byrne et al.
[cited by applicant]
U.S. Appl. No. 17/766,680, filed Apr. 5, 2022, Liu et al.
[cited by applicant]
U.S. Appl. No. 17/953,292, filed Sep. 26, 2022, Monian et al.
[cited by applicant]
U.S. Appl. No. 17/956,741, filed Sep. 29, 2022, Vargeese et al.
[cited by applicant]
U.S. Appl. No. 17/960,090, filed Oct. 4, 2022, Vargeese et al.
[cited by applicant]
U.S. Appl. No. 18/062,422, filed Dec. 6, 2022, Butler et al.
[cited by applicant]
U.S. Appl. No. 18/178,470, filed Mar. 3, 2023, Vargeese et al.
[cited by applicant]
U.S. Appl. No. 18/204,895, filed Jun. 1, 2023, Vargeese et al.
[cited by applicant]
U.S. Appl. No. 18/252,029, filed May 5, 2023, Monian et al.
[cited by applicant]
U.S. Appl. No. 18/316,932, filed May 12, 2023, Butler et al.
[cited by applicant]
Agrawal, S. et al., Mixed-backbone oligonucleotides as second generation antisense oligonucleotides: In vitro and in vivo studies, Proc. Natl. Acad. Sci. USA, 94: 2620-2625 (1997).
[cited by applicant]
Bilesen, P.H.J. et al., Identification and Allele-Specific Silencing of the Mutant Huntingtin Allele in Huntington's Disease Patient-Derived Fibroblasts, Hum. Gene Thera., 19:710-718 (2008).
[cited by applicant]
Bock, L.C. et al., Selections of single-stranded DNA molecules that bind and inhibit human thrombin, Nature, 355: 564-566 (1992).
[cited by applicant]
Boyanapalli, R. et al., A Novel Quantitative Wild-type Huntingtin (wtHTT) Protein Biomarker Method for Human Cerebrospinal Fluid, Wave Life Sciences, presented at the 17th Annual Huntington's Disease Therapeutics Confer…
[cited by applicant]
Carroll, J. B. et al., Potent and Selective Antisense Oligonucleotides Targeting Single-Nucleotide Polymorphisms in the Huntington Disease Gene / Allele-Specific Silencing of Mutant Huntingtin, Mol. Thera., 19(12):2178-…
[cited by applicant]
Chan, J.H.P. et al., Antisense Oligonucleotides: From Design to Therapeutic Application, Clinical and Experimental Pharmacology and Physiology, 33: 544-540 (2006).
[cited by applicant]
Crooke, S. T., Antisense Drug Technology: Principles, Strategies, and Applications, 2nd Edition, pp. 1-66 (2008).
[cited by applicant]
Crooke, S. T., Antisense Strategies, Curr. Mol. Med., 4(5):465-487 (2004).
[cited by applicant]
Crooke, S.T., Progress in Antisense Technology , Annu. Rev. Med., 55: 61-95 (2004).
[cited by applicant]
Dale, E., Enhancing the pharmacologic profiles of CNS targeting therapeutic oligonucleotides, Wave Life Sciences, presented at TIDES USA, on Sep. 23, 2021.
[cited by applicant]
Engelhardt, J.A. et al., Scientific and Regulatory Policy Committee Points-to-consider Paper: Drug-induced Vascular Injury Associated with Nonsmall Molecule Therapeutics in Preclinical Development: Part 2. Antisense Oli…
[cited by applicant]
Frazier, K. et al., Potential Mechanisms of vascular toxicity in Monkeys with antisense oligonucleotides, TIDES oligo conference, 1-25 (May 15, 2014).
[cited by applicant]
Frazier, K.S. Antisense Oligonucleotide Therapies: The Promise and the Challenges from a Toxicologic Pathologist's Perspective, Toxicology Pathology, 43: 78-89 (2015).
[cited by applicant]
Gagnon, K. T. et al., Allele-Selective Inhibitions of Mutant Huntingtin Expression with Antisense Oligonucleotide Targeting the Expanded CAG Repeat, Biochemistry 49(47): 10166-10178 (2010).
[cited by applicant]
Gagnon, K.T. and Watts, J.K 10th Annual Meeting of the Oligonucleotide Therapeutics Society, San Diego, CA, Summer Summaries (Oct. 12-15, 2014).
[cited by applicant]
Hartmann, G. et al., Delineation of a CpG Phosphorothioate Oligodeoxynucleotide for Activating Primate Immune Responses In Vitro and In Vivo, The Journal of Immunology, 164(3): 1617-1624 (2000).
[cited by applicant]
Henry, S.P. et al., Activation of the Alternative Pathway of Complement by a Phosphorothioate Oligonucleotide: Potential Mechanism of Action, The Journal of Pharmacology and Experimental Therapeutics, 281(2): 810-816 (1…
[cited by applicant]
Hu, J. et al., Allele-Selective Inhibition of Huntingtin Expression by Switching to an miRNA-like RNAi Mechanism, Chemistry & Biology 17: 1183-1188 (2010).
[cited by applicant]
Hu, J. et al., Exploring the Effect of Sequence Length and Composition on Allele-Selective Inhibition of Human Huntingtin Expression by Single-Stranded Silencing RNAs, Nucleic Acid Therapeutics, 24(3): 199-209 (2014).
[cited by applicant]
Hung, S. Stereopure oligonucleotides as a therapeutic approach to rare neurological diseases. Paper presented at: Huntington's Society of Canada 2017 National Conference (Nov. 2017).
[cited by applicant]
International Search Report for PCT/US2016/043598, 4 pages (Nov. 28, 2016).
[cited by applicant]
Ionis Pharmaceuticals, Inc., Ionis Pharmaceuticals Licenses IONIS-HTT Rx to Partner Following Successful Phase 1/2a Study in Patients with Huntington's Disease, Press Release, 2 pages (Dec. 11, 2017).
[cited by applicant]
Iwamoto, N. et al., Control of phosphorothioate stereochemistry substantially increases the efficacy of antisense oligonucleotides, Nature Biotechnol, 35(9): 845-851 (2017), with Supplemental Data, 14 pages.
[cited by applicant]
Iwamoto, N. et al., Control of phosphorothioate stereochemistry substantially increases the efficacy of antisense oligonucleotides, Nature Biotechnology, 1-7 pages (2017). All Supplemental Data, 8-53 pages (2017).
[cited by applicant]
Iwamoto, N. et al., Optimization of Therapeutic Phosphorothioate Oligonucleotides by P-Chirality Control, WAVE Life Sciences, PSJ Congress: The Pharmaceutical Society of Japan, (Mar. 25, 2015-Mar. 28, 2016).
[cited by applicant]
Iwamoto, N. From Stereopurity to precision medicine: Optimizing the properties of antisense nucleic acid therapeutics. Paper presented at: BioJapan, Yokohama, Japan (Oct. 11, 2018).
[cited by applicant]
Kandasamy, P. et al., From stereopurity to precision medicine: Optimizing the properties of antisense nucleic acid therapeutics. Paper presented at: the 45th International Symposium on Nucleic Acid Chemistry, Kyoto, Jap…
[cited by applicant]
Kaur, H. et al., Activation of natural killer-like YT-INDY cells by oligodeoxynucleotides and binding by homologous pattern recognition proteins, Scandinavian Journal of Immunology, 62: 361-370 (2005).
[cited by applicant]
Kay, C. et al., Personalized gene silencing therapeutics for Huntington disease, Clinical Genetics, 1-8 (2014).
[cited by applicant]
Koziolkewicz et al., Stability of Stereoregular Oligo-(nucleoside Phosphorothioate)s in Human Plasma: Diastereoselectiviy of Plasma 3′-Exonuclease, Antisense Nucl. Acid Drug Dev., 7: 43-48 (1997).
[cited by applicant]
Koziolkiewicz, M. et al., Effect of P-chirality of oligo(deoxyribonucleoside phosphorothioate)s) on the activity of terminal deoxyribonucleotidyl transferase, FEBS Letters, 434(1-2): 77-82 (1998).
[cited by applicant]
Krakowiak, A. et al., Influence of P-Chirality of Phosphorothioate Oligonucleotides on the Activity of Amv-Reverse Transcriptase, Nucleosides & Nucleotides, 17(9-11): 1823-1834 (1998).
[cited by applicant]
Krieg, A.M. et al., P-Chirality-Dependent Immune Activiation by Phosphorothioate CpG Oligodeoxynucleotides, Oligonucleotides, 13:491-499 (2003).
[cited by applicant]
Leviten, M., Wave's Purity Progress, Biocentury, 1-6 (Sep. 28, 2017).
[cited by applicant]
Liu, Y. et al., Impact of Nitrogen-containing Backbone Linkages on Stereopure Antisense Oligonucleotides in the CNS, Wave Life Sciences, Presented at TIDES USA: Oligonucleotide & Peptide Therapeutics on Sep. 20-23, 2021…
[cited by applicant]
McBride, J.L. et al., Prelinical Safety of RNAi-Mediated HTT Suppression in the Rhesus Macaque as a Potential Therapy for Huntington's Disease, Molecular Therapy, 19: 1-11 (2011).
[cited by applicant]
Meena, Control of Human RNase H Mediated Cleavage by Stereopure Phosphorothioate Oligonucleotides, WAVE Life Sciences, TIDES Meeting, 23 pages (May 3-6, 2015).
[cited by applicant]
Meena, Development of Allele Specific Antisense Oligonucleotides, WAVE Life Sciences, ACS Central Regional Meeting (CERM), Covington, KY (May 19, 2016).
[cited by applicant]
Meena, Development of Allele Specific Antisense Oligonucleotides, WAVE Life Sciences, TIDES Meeting (May 11, 2016).
[cited by applicant]
Meena, et al., Discovery and Early Clinical Development of the First Allele-Specific Stereopure ASO Drug Candidate with Disease—Modifying Potential for the Treatment of Huntington's Disease, WAVE Life Sciences, Poster, …
[cited by applicant]
Meena, et al., Therapeutic Implications of Controlling P-Chirality in Phosphorothioate Oligonucleotides, TIDES Poster (May 12-15, 2014).
[cited by applicant]
Meena, et al., Therapeutic Implications of Controlling P-Chirality in Phosphorothioate Oligonucleotides, TIDES, San Diego, WAVE Life Sciences, Poster, 1 page (May 3-6, 2014).
[cited by applicant]
Meena, Optimization of Antisense Drugs by P-Stereochemistry Control, WAVE Life Sciences, OTS Annual Meeting 2014, Oligonucleotide Therapeutics Society, 13 pages (Oct. 12-14, 2014).
[cited by applicant]
Midturi, J. et al., Spectrum of Pulmonary Toxicity Associated with the Use of Interferon Therapy for Hepatitis C: Case Report and Review of the Literature, Clinical Infectious Diseases, 39(11): 1724-1729 (2004).
[cited by applicant]
Miniarikova, J. et al., Design Characterization, and Lead Selection of Therapeutic miRNAs Targeting Huntingtin for Development of Gene Therapy for Huntington's Disease, Molecular Therapy-Nucleic Acids, 5(3): e297 (2016).
[cited by applicant]
Mohapatra, S. LCMS/hybridization ELISA approaches for bioanalysis of stereopure oligonucleotides. Paper presented at: American Association of Pharmaceutical Scientists Annual Meeting, Washington, DC USA (Nov. 4-7, 2018).
[cited by applicant]
Mujeeb, A. et al., High-Resolution NMR of an Antisense DNA.RNA Hybrid Containing Alternating Chirally Pure R p Methylphosphonates in the DNA Backbone+, 36(9): 2371-2379 (1997).
[cited by applicant]
Ostergaard, M.E. et al., Differential effects on allele selective silencing of mutant huntingtin by two stereoisomers of α,β-constrained nucleic acid, ACS Chem. Biol., 9(9):1975-1979 (2014).
[cited by applicant]
Panzara, M. A. Stereopure Oligonucleotides in Development for the Treatment of Genetically Defined Diseases, Wave Life Sciences, presented at TIDES Boston Virtual Conference on Sep. 15-18, 2020.
[cited by applicant]
Panzara, M. et al., Stereopure nucleic acid therapies in development for the treatment of genetic neurological diseases, Poster presented at: 19th Annual Meeting of the American Society of Experimental Neurotherapeutics…
[cited by applicant]
Panzara, M. Stereopure nucleic acid therapies in development for the treatment of genetic neurological diseases, Neurotherapeutics, Abstract, 14: 821-822 (2017).
[cited by applicant]
Panzara, M. Stereopure nucleic acid therapies in development for the treatment of genetic neurological diseases, Paper presented at: 19th Annual Meeting of the American Society of Experimental Neurotherapeutics, Rockvil…
[cited by applicant]
Panzara, M. Stereopure nucleic acid therapies in development for the treatment of genetic neurological diseases. Paper presented at: International Society for CNS Drug Development (ISCDD) Annual Meeting, Las Vegas, NV U…
[cited by applicant]
Panzara, M., Innovations that led to SELECT-HD, a phase 1b/2a clinical trial of an allele-selective therapy for Huntington's Disease, Wave Life Sciences, presented on Mar. 3, 2022.
[cited by applicant]
Patil et al., Syntheses and properties of oligothymidylate analogs containing stereoregulated phosphorothioate and phosphodiester linkages in an alternating manner, Bioorganic & Medicinal Chemistry Letters, 4(22): 2663-…
[cited by applicant]
Pedersen, L. et al., A Kinetic Model Explains Why Shorter and Less Affine Enzyme-recruiting Oligonucleotides Can Be More Potent, Mol Ther Nucleic Acids, 3: e149 1-8 (2014).
[cited by applicant]
Pharmacology Review(s), Application No. 203568Orig1s000, Center for Drug Evaluation and Research, Food and Drug Administration, Department of Health & Human Services, 2013.
[cited by applicant]
Pontarollo, R.A et al., Monocytes are required for optimum in vitro stimulation of bovine peripheral blood mononuclear cells by non-methylated CpG motifs, Veterinary Immunology and Immunopathology, 84(1-2): 43-59 (2002).
[cited by applicant]
Prakash, T.P. et al., 2′-O-[2-(Methylthio )ethyl]-Modified Oligonucleotide: An Analogue of 2′-O-[2-(Methoxy)-ethyl]-Modified Oligonucleotide with Improved Protein Binding Properties and High Binding Affinity to Target R…
[cited by applicant]
Robinson, D.S. et al., Predominant TH2-Like Bronchoalveolar T-Lymphocyte Population in Atopic Asthma, The New England Journal of Medicine, 326: 298-304 (1992).
[cited by applicant]
Senn, J.J. et al., Non-CpG-Containing Antisense 2′-Methoxyethyl Oligonucleotides Activate a Proinflammatory Response Independent of Toll-Like Receptor 9 or Myeloid DifferentiationFactor 88, The Journal of Pharmacology a…
[cited by applicant]
Seth, P., and Olson, R., Nucleic Acid Therapeutics—Making Sense of Antisesnse, 2016 Drug Design and Delivery Symposium, ACS Webinar, 1-36 (Jul. 26, 2016).
[cited by applicant]
Sheehan, J.P. and Phan, T.M. Phosphorothioate Oligonucleotides Inhibit the Intrinsic Tenase Complex by an Allosteric Mechanism, Biochemistry, 40: 4980-4989 (2001).
[cited by applicant]
Singhrao, S.K. et al., Increased Complement Biosynthesis by Microglia and Complement Activation on Neurons in Huntington's Disease, Experimental Neurology, 159: 362-376 (1999).
[cited by applicant]
Soldatow, V.Y. et al., In vitro models for liver toxicity testing, Toxicol Res, 2(1):23-39 (2013).
[cited by applicant]
Southwell, A. L. et al., In Vivo Evaluation of Candidate Allele-specific Mutant Huntingtin Gene Silencing Antisense Oligonucleotides, Mol. Thera., 22(12):2093-2106 (2014).
[cited by applicant]
Stec, W.J. et al., Deoxyribonucleoside 3′-O-(2-Thio- and 2-Oxo-“spiro”-4,4-pentamethylene-1,3,2-oxathiaphospholane)s: Monomers for Stereocontrolled Synthesis of Oligo(deoxyribonucleoside phosphorothioate)s and Chimeric …
[cited by applicant]
Tosquellas, G. et al., Prooligonucleotides exhibit less serum-protein binding than phosphodiester and phosphorothioate oligonucleotides, Nucleosides, Nucleotides and Nucleic Acids, 19(5-6):995-1003 (2000).
[cited by applicant]
Vargeese, C. From Stereopurity to precision medicine: Optimising the properties of antisense nucleic acid therapeutics, Paper presented at: TIDES Europe: Oligonucleotide and Peptide Therapeutics, Amsterdam, The Netherla…
[cited by applicant]
Vargeese, C. From Stereopurity to precision medicine: Optimizing the properties of antisense nucleic acid therapeutics, Paper presented at: Nature Conference on RNA at the Bench and Bedside, La Jolla, CA USA (Oct. 8, 20…
[cited by applicant]
Vargeese, C. Pharmacologic properties of stereopure oligonucleotides. Paper presented at: 44th International Symposium on Nucleic Acids Chemistry, Tokyo, Japan (Nov. 14-16, 2017).
[cited by applicant]
Vargeese, C. Stereochemical control of antisense oligonucleotides enhances target efficacy. Paper presented at: the 14th Annual Meeting of the Oligonucleotide Therapeutic Society, Seattle, WA USA (Oct. 3, 2018).
[cited by applicant]
Vergeese, C., Exploring new oligonucleotide backbone chemistries and their deployment to improve the properties of stereopure oligonucleotides, Wave Life Sciences, presented at TIDES USA on Sep. 22, 2021.
[cited by applicant]
Vickers, T. A. et al., Efficient Reduction of Target RNAs by Small Interfering RNA and RNase H-dependent Antisense Agents, Jrnl. Bio. Chem., 278(9):7108-7118 (2003).
[cited by applicant]
Viglietta, V., Select-HD: an adaptive first-in-human clinical trial to evaluate WVE-003, an investigational allele selective mHTT-lowering oligonucleotide, in early manifest Huntington's disease, Wave Life Sciences, pre…
[cited by applicant]
Wan, W.B. and Seth, P.P., The Medicinal Chemistry of Therapeutic Oligonucleotides, J. Med. Chem., 59: 9645-9667 (2016).
[cited by applicant]
Wan, W.B. et al., Synthesis, biophysical properties and biological activity of second generation antisense oligonucleotides containing chiral phosphorothioate linkages, Nucleic Acid Research, 42(22):13456-13468 (2014). …
[cited by applicant]
WAVE Life Sciences, Second Quarter 2022 Earnings Presentation, 27 pages, (2022).
[cited by applicant]
WAVE Life Sciences, WAVE Life Sciences Corporate Presentation, 32 pages, Aug. 3, 2023.
[cited by applicant]
WAVE Life Sciences, WAVE Life Sciences Corporate Presentation, 63 pages, May 12, 2022.
[cited by applicant]
Woolf, T.M. et al., Specificity of antisense oligonucleotides in vivo, Prov. Natl. Aca. Sci. USA, 89: 7305-7309 (1992).
[cited by applicant]
Wozniak, L.A. et al., Chirality at phosphorus: hybrid duplexes of chimeric oligonucleotides containing methylphosphonothioate linkages with complementary DNA and RNA, Journal of Organometallic Chemistry, 690(10): 2658-2…
[cited by applicant]
Written Opinion for PCT/US2016/043598, 10 pages (Nov. 28, 2016).
[cited by applicant]
Xu, D. and Esko, J.D., Demystifying Heparan Sulfate- Protein Interactions, Annu. Rev. Biochem., 83: 129-157 (2014).
[cited by applicant]
Zhang, Y. et al., Structural Isosteres of Phosphate Groups in the Protein Data Bank, J. Chem. Inf. Model, 1-18 (2017).
[cited by applicant]
Zhang, Y., Investigating phosphate structural replacements through computational and experimental approaches, Academic Dissertain, University of Helsinki, 119 pages (2014).
[cited by applicant]
Zhong, Z. et al., WAVE Life Sciences: Developing Stereopure Nucleic Acid Therapies for the Treatment of Genetic Neurological Diseases, World CNS Summit 2017, Boston, MA, WAVE Life Sciences, Poster, 1 page (Feb. 20-22, 2…
[cited by applicant]
Zhong, Z. Stereochemical control of antisense oligonucleotides enhances target efficacy. Paper presented at: TIDES: Oligonucleotide and Peptide Therapeutics, Boston, MA USA (May 9, 2018).
[cited by applicant]
Zhong, Z. WAVE Life Sciences: Developing stereopure nucleic acid therapies for the treatment of serious genetically defined diseases, Paper presented at: ALS Drug Discovery Roundtable Meeting, Boston, MA (Apr. 25, 2017).
[cited by applicant]
Zon, Automated synthesis of phosphorus-sulfur analogs of nucleic acids—25 years on: potential therapeutic agents and proven utility in biotechnology, New J. Chem., 34(5): 795-804 (2010).
[cited by applicant]
U.S. Appl. No. 18/522,146, filed Nov. 28, 2023, Butler et al.
[cited by applicant]
U.S. Appl. No. 18/613,034, filed Mar. 21, 2024, Vargeese et al.
[cited by applicant]
U.S. Appl. No. 18/695,346, filed Mar. 25, 2024, Monian et al.
[cited by applicant]
U.S. Appl. No. 18/695,348, filed Mar. 25, 2024, Acker et al.
[cited by applicant]
U.S. Appl. No. 18/704,629, filed Apr. 25, 2024, Byrne et al.
[cited by applicant]
U.S. Appl. No. 18/836,993, filed Aug. 8, 2024, Kandasamy et al.
[cited by applicant]
U.S. Appl. No. 18/843,171, filed Aug. 30, 2024, Hu et al.
[cited by applicant]
U.S. Appl. No. 18/856,553, filed Oct. 11, 2024, Lu et al.
[cited by applicant]
U.S. Appl. No. 18/864,860, filed Nov. 11, 2024, Shivalila et al.
[cited by applicant]
U.S. Appl. No. 18/864,863, filed Nov. 11, 2024, Liu et al.
[cited by applicant]
U.S. Appl. No. 18/942,334, filed Nov. 8, 2024, Yang et al.
[cited by applicant]
U.S. Appl. No. 18/953,020, filed Nov. 19, 2024, Meena et al.
[cited by applicant]
U.S. Appl. No. 19/008,522, filed Jan. 2, 2025, Vargeese et al.
[cited by applicant]
Wang, L. et al., Phosphorothioation of DNA in bacteria by dnd genes, Nat. Chem. Biol., 3(11):709-710 (2007).
[cited by applicant]