IP Library Assignment 071218/0445
Patent Assignment
Reel/Frame 071218/0445

Security Interest

Recorded: 2025-05-07 Pages: 25
Assignor
SAREPTA THERAPEUTICS, INC.
Executed: 2025-02-13
Assignee
JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT
10 S. DEARBORN ST., L2, CHICAGO, ILLINOIS, 60603
Covered Properties (147)
Multiple Exon Skipping Compositions for Dmd
Application: 18/778,132 →
Publication: US US20250154507A1
Oligonucleotides for Treating Expanded Repeat Diseases
Application: 18/310,922 →
Publication: US US20240209363A1
Compositions for Treating Muscular Dystrophy
Application: 18/541,286 →
Compositions for Treating Muscular Dystrophy
Application: 18/814,323 →
Publication: US US20260117225A1
Compositions for Treating Muscular Dystrophy
Application: 18/966,357 →
Publication: US US20260117227A1
Exon Skipping Compositions for Treating Muscular Dystrophy
Application: 18/885,116 →
Publication: US US20250236869A1
Exon Skipping Compositions for Treating Muscular Dystrophy
Application: 18/885,088 →
Publication: US US20250145991A1
Peptide Oligonucleotide Conjugates
Application: 18/296,697 →
Publication: US US20230310625A1
Peptide Oligonucleotide Conjugates
Application: 19/029,784 →
Publication: US US20260014263A1
Antisense-Induced Exon Exclusion in Type Vii Collagen
Application: 18/410,720 →
Publication: US US20240415857A1
Modified Antisense Oligomers for Exon Inclusion in Spinal Muscular Atrophy
Application: 18/813,696 →
Publication: US US20250241940A1
Peptide Oligonucleotide Conjugates
Application: 18/658,614 →
Publication: US US20250057965A1
Processes for Preparing Phosphorodiamidate Morpholino Oligomers
Application: 17/169,611 →
Publication: US US20220340605A1
Antisense Oligomers and Methods of Using the Same for Treating Diseases Associated with the Acid Alpha-Glucosidase Gene
Application: 18/910,901 →
Publication: US US20250171779A1
Phosphorodiamidate Morpholino Oligomers
Application: 17/841,185 →
Publication: US US20230045831A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 18/181,271 →
Publication: US US20230381216A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 17/804,280 →
Publication: US US20220387601A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 18/807,055 →
Publication: US US20250064959A1
Antisense Oligomer Compounds
Application: 18/145,604 →
Publication: US US20230407301A1
Exon Skipping Oligomers for Muscular Dystrophy
Application: 16/973,464 →
Publication: US US20220251551A1
Treatment Methods for Muscular Dystrophy
Application: 17/732,757 →
Publication: US US20230193282A1
Exon Skipping Oligomers and Oligomer Conjugates for Muscular Dystrophy
Application: 18/634,360 →
Publication: US US20250092393A1
Compositions for Treating Muscular Dystrophy
Application: 17/603,229 →
Publication: US US20220193246A1
Exon Skipping Oligomers and Oligomer Conjugates for Muscular Dystrophy
Application: 18/440,684 →
Publication: US US20250090569A1
Exon Skipping Oligomers for Muscular Dystrophy
Application: 18/484,970 →
Publication: US US20240344067A1
Compositions Comprising Exon Skipping Oligonucleotide Conjugates for Treating Muscular Dystrophy
Application: 18/257,547 →
Publication: US US20240327831A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 18/744,061 →
Publication: US US20250179487A1
Methods for Treating Muscular Dystrophy
Application: 17/618,100 →
Publication: US US20220296633A1
Methods for Treating Muscular Dystrophy with Casimersen
Application: 17/441,620 →
Publication: US US20220152086A1
Adeno-Associated Virus Antibodies and Fragments Thereof
Application: 17/348,356 →
Publication: US US20210388064A1
Methods for Analyzing Aav Capsid Proteins
Application: 17/782,472 →
Publication: US US20230204595A1
Methods of Treating Muscular Dystrophy
Application: 18/876,051 →
Publication: US US20260002175A1
Systemic Delivery of Adeno-Associated Virus Vector Expressing Gamma-Sarcoglycan and the Treatment of Muscular Dystrophy
Application: 18/444,018 →
Publication: US US20240374684A1
Phosphorodiamidate Morpholino Oligomer Conjugates
Application: 18/842,988 →
Publication: US US20250195667A1
Suspension Mode Seed Train Development for Adherent Cells
Application: 18/255,221 →
Publication: US US20240018487A1
Production of Recombinant Aav Vectors for Treating Muscular Dystrophy
Application: 18/562,148 →
Publication: US US20250018059A1
Formulation of an Antisense Oligomer Conjugate
Application: 18/500,627 →
Publication: US US20240218365A1
Antisense Oligonucleotides Having One or More Abasic Units
Application: 18/693,769 →
Publication: US US20240425864A1
Recombinant Aav Vectors for Treating Muscular Dystrophy
Application: 63/509,221 →
Recombinant Aav Vectors for Treating Muscular Dystrophy
Application: 63/518,055 →
Genetic Constructs for Gene Editing
Application: 63/635,770 →
Genetic Constructs for Gene Editing
Application: 63/683,285 →
Treatment of Genetic Neurological Conditions with Genomic Editing
Application: 63/638,225 →
Muscle Tropic Raav
Application: 63/654,224 →
Muscle Tropic Raav
Application: 63/660,638 →
Antisense Oligomers for Treatment of Chronic Kidney Disease
Application: 18/647,899 →
Publication: US US20250066776A1
Humanized Umod Mouse Model Generation, Characterization and Methods of Use
Application: 63/564,345 →
Dystrophin and Micro-Dystrophin Antibodies and Fragments Thereof
Application: 63/701,661 →
Dose Packaging System for Medication and Method of Storing Dose Therein
Application: 18/750,827 →
Publication: US US20250387299A1
Aav Transfer Cassette
Application: 17/072,637 →
Publication: US US20210128652A1
Adeno-Associated Virus Vectors for Treatment of Rett Syndrome
Application: 18/022,059 →
Publication: US US20230304038A1
Adeno-Associated Virus Vectors for Treatment of Rett Syndrome
Application: 18/680,380 →
Publication: US US20240392316A1
Raav Production Methods
Application: 63/448,872 →
Oligonucleotide Compound and Method for Treating Nidovirus Infections
Patent: 8,759,307 →
Application: 12/109,856 →
Publication: US US20090012280A1
ANTISENSE ANTIVIRAL COMPOUND AND METHOD FOR TREATING ss/RNA VIRAL INFECTION
Application: 14/535,092 →
Publication: US US20150267202A1
Antisense Antiviral Compounds and Methods for Treating a Filovirus Infection
Patent: 8,198,429 →
Application: 12/853,180 →
Publication: US US20120035136A1
Antisense Antiviral Compounds and Methods for Treating a Filovirus Infection
Patent: 8,524,684 →
Application: 13/469,892 →
Publication: US US20130011420A1
Antisense Antiviral Compounds and Methods for Treating a Filovirus Infection
Patent: 8,703,735 →
Application: 13/957,261 →
Publication: US US20140044750A1
Antisense Antiviral Compounds and Methods for Treating a Filovirus Infection
Patent: 9,382,536 →
Application: 14/196,975 →
Publication: US US20150275204A1
Antisense Antiviral Compounds and Methods for Treating a Filovirus Infection
Patent: 9,982,261 →
Application: 15/132,028 →
Publication: US US20170306323A1
Antisense Composition and Method for Treating Muscle Atrophy
Patent: 7,888,012 →
Application: 11/433,724 →
Publication: US US20070122821A1
Antisense Composition and Method for Treating Muscle Atrophy
Patent: 8,785,410 →
Application: 12/983,798 →
Publication: US US20110166082A1
Antisense Composition and Method for Treating Muscle Atrophy
Application: 15/177,244 →
Publication: US US20160281092A1
Antisense Composition and Method for Treating Muscle Atrophy
Application: 15/986,746 →
Publication: US US20180327749A1
Antisense Antibacterial Method and Compound
Patent: 7,790,694 →
Application: 11/487,009 →
Publication: US US20070135333A1
Antibacterial Antisense Oligonucleotide and Method
Patent: 8,067,571 →
Application: 11/803,107 →
Publication: US US20080194463A1
Antibacterial Antisense Oligonucleotide and Method
Patent: 8,536,147 →
Application: 12/723,413 →
Publication: US US20100234281A1
Antibacterial Antisense Oligonucleotide and Method
Patent: 9,249,243 →
Application: 13/963,919 →
Publication: US US20140213737A1
Antibacterial Antisense Oligonucleotide and Method
Patent: 9,499,583 →
Application: 14/977,451 →
Publication: US US20160251398A1
Antibacterial Antisense Oligonucleotide and Method
Application: 15/293,961 →
Publication: US US20170247410A1
Oligonucleotide Analogs Having Cationic Intersubunit Linkages
Patent: 7,943,762 →
Application: 11/801,885 →
Publication: US US20090088562A1
Compound and Method for Treating Myotonic Dystrophy
Patent: 8,741,863 →
Application: 13/219,401 →
Publication: US US20120058946A1
Compound and Method for Treating Myotonic Dystrophy
Patent: 8,835,402 →
Application: 14/038,314 →
Publication: US US20140107013A1
Compound and Method for Treating Myotonic Dystrophy
Application: 14/261,120 →
Publication: US US20150080311A1
Compound and Method for Treating Myotonic Dystrophy
Application: 14/464,561 →
Publication: US US20150141321A1
Compound and Method for Treating Myotonic Dystrophy
Application: 16/163,948 →
Publication: US US20190264210A1
Method of Synthesis of Morpholino Oligomers
Patent: 8,299,206 →
Application: 12/271,036 →
Publication: US US20090131632A1
Synthesis of Morpholino Oligomers Using Doubly Protected Guanine Morpholino Subunits
Patent: 8,076,476 →
Application: 12/271,040 →
Publication: US US20090131624A1
Multiple Exon Skipping Compositions for Dmd
Patent: 8,865,883 →
Application: 13/830,253 →
Publication: US US20130190390A1
Multiple Exon Skipping Compositions for Dmd
Patent: 9,447,417 →
Application: 14/858,416 →
Publication: US US20160002637A1
Multiple Exon Skipping Compositions for Dmd
Patent: 8,871,918 →
Application: 12/605,276 →
Publication: US US20100130591A1
Multiple Exon Skipping Compositions for Dmd
Patent: 9,434,948 →
Application: 14/852,264 →
Publication: US US20150376618A1
Multiple Exon Skipping Compositions for Dmd
Patent: 9,234,198 →
Application: 14/852,257 →
Publication: US US20150376617A1
Multiple Exon Skipping Compositions for Dmd
Patent: 9,447,416 →
Application: 14/857,569 →
Publication: US US20160002633A1
Multiple Exon Skipping Compositions for Dmd
Patent: 9,453,225 →
Application: 14/857,590 →
Publication: US US20160002634A1
Antisense Antiviral Compound and Method for Treating Influenza Viral Infection
Patent: 8,697,858 →
Application: 12/945,081 →
Publication: US US20110118334A1
Antisense Antiviral Compound and Method for Treating Influenza Viral Infection
Patent: 9,394,323 →
Application: 14/251,124 →
Publication: US US20140303073A1
Antisense Modulation of Interleukins 17 and 23 Signaling
Patent: 9,238,042 →
Application: 13/107,528 →
Publication: US US20110289608A1
Oligonucleotide Analogues Having Modified Intersubunit Linkages and/or Terminal Groups
Patent: 8,779,128 →
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Publication: US US20120065169A1
Oligonucleotide Analogues Having Modified Intersubunit Linkages and/or Terminal Groups
Patent: 9,469,664 →
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Publication: US US20150073140A1
Oligonucleotide Analogues Having Modified Intersubunit Linkages and/or Terminal Groups
Application: 15/247,584 →
Publication: US US20170198287A1
Oligonucleotide Analogues Having Modified Intersubunit Linkages and/or Terminal Groups
Application: 16/225,909 →
Publication: US US20190218551A1
dsRNA MOLECULES COMPRISING OLIGONUCLEOTIDE ANALOGS HAVING MODIFIED INTERSUBUNIT LINKAGES AND/OR TERMINAL GROUPS
Application: 13/819,634 →
Publication: US US20130288369A1
Dsrna Molecules Comprising Oligonucleotide Analogs Having Modified Intersubunit Linkages and/or Terminal Groups
Application: 16/028,878 →
Publication: US US20190169611A1
Functionally-Modified Oligonucleotides and Subunits Thereof
Patent: 9,278,987 →
Application: 14/358,992 →
Publication: US US20140330006A1
Functionally-Modified Oligonucleotides and Subunits Thereof
Patent: 9,790,499 →
Application: 15/007,017 →
Publication: US US20160376587A1
Functionally-Modified Oligonucleotides and Subunits Thereof
Application: 15/700,718 →
Publication: US US20180223278A1
Functionally-Modified Oligonucleotides And Subunits Thereof
Application: 16/416,574 →
Publication: US US20200115709A1
Peptide Oligonucleotide Conjugates
Patent: 9,161,948 →
Application: 13/299,310 →
Publication: US US20120289457A1
Peptide Oligonucleotide Conjugates
Patent: 9,862,946 →
Application: 14/851,434 →
Publication: US US20160237426A1
Peptide Oligonucleotide Conjugates
Application: 15/827,431 →
Publication: US US20180298383A1
Peptide Oligonucleotide Conjugates
Application: 16/593,615 →
Publication: US US20200277598A1
Peptide Oligonucleotide Conjugates
Application: 16/869,213 →
Publication: US US20210139896A1
Induced Exon Inclusion in Spinal Muscle Atrophy
Patent: 9,944,926 →
Application: 14/360,895 →
Publication: US US20140329772A1
Induced Exon Inclusion in Spinal Muscle Atrophy
Application: 15/921,518 →
Publication: US US20180273954A1
Oligonucleotides for Treating Expanded Repeat Diseases
Application: 14/360,890 →
Publication: US US20140303238A1
Oligonucleotides for Treating Expanded Repeat Diseases
Application: 16/038,580 →
Publication: US US20190100755A1
Oligonucleotide Analogues Targeting Human Lmna
Patent: 9,066,967 →
Application: 13/708,708 →
Publication: US US20140024821A1
Oligonucleotide Analogues Targeting Human Lmna
Patent: 9,682,097 →
Application: 14/709,355 →
Publication: US US20160102307A1
Oligonucleotide Analogues Targeting Human Lmna
Application: 15/595,820 →
Publication: US US20180092938A1
Oligonucleotide Analogues Targeting Human Lmna
Application: 16/387,002 →
Publication: US US20200147119A1
Boronic Acid Conjugates of Oligonucleotide Analogues
Patent: 9,920,085 →
Application: 14/386,720 →
Publication: US US20150080340A1
Compositions for Treating Muscular Dystrophy
Patent: 9,506,058 →
Application: 14/214,567 →
Publication: US US20140315862A1
Compositions for Treating Muscular Dystrophy
Application: 15/359,152 →
Publication: US US20170283799A1
Compositions for Treating Muscular Dystrophy
Application: 15/604,335 →
Publication: US US20180105811A1
Exon Skipping Compositions for Treating Muscular Dystrophy
Patent: 9,217,148 →
Application: 14/213,607 →
Publication: US US20140323544A1
Exon Skipping Compositions for Treating Muscular Dystrophy
Application: 16/220,799 →
Publication: US US20190177724A1
Exon Skipping Compositions for Treating Muscular Dystrophy
Application: 17/130,716 →
Publication: US US20210180064A1
Antisense-Induced Exon Exclusion in Myostatin
Application: 15/559,257 →
Publication: US US20180355358A1
Peptide Oligonucleotide Conjugates
Application: 15/574,734 →
Publication: US US20180214567A1
Peptide Oligonucleotide Conjugates
Application: 16/860,292 →
Publication: US US20200254109A1
Peptide Oligonucleotide Conjugates
Application: 17/403,403 →
Publication: US US20220072143A1
Antisense-Induced Exon Exclusion in Type Vii Collagen
Application: 15/578,612 →
Publication: US US20190201425A1
Antisense-Induced Exon Exclusion in Type Vii Collagen
Application: 17/080,363 →
Publication: US US20210161922A1
Methods and Compounds for Treatment of Lymphocyte-Related Diseases and Conditions
Application: 15/579,497 →
Publication: US US20180161359A1
Modified Antisense Oligomers for Exon Inclusion in Spinal Muscular Atrophy
Application: 15/754,782 →
Publication: US US20190015440A1
Modified Antisense Oligomers for Exon Inclusion in Spinal Muscular Atrophy
Application: 16/949,980 →
Publication: US US20210169918A1
Processes for Preparing Oligomers
Application: 16/303,356 →
Publication: US US20200040020A1
Processes for Preparing Oligomers
Application: 17/098,935 →
Publication: US US20210198296A1
Processes for Preparing Phosphorodiamidate Morpholino Oligomers
Application: 16/302,443 →
Publication: US US20190276480A1
Antisense Oligomers and Methods of Using the Same for Treating Diseases Associated with the Acid Alpha-Glucosidase Gene
Application: 16/094,858 →
Publication: US US20190284555A1
Antisense Oligomers and Methods of Using the Same for Treating Diseases Associated with the Acid Alpha-Glucosidase Gene
Application: 17/343,447 →
Publication: US US20220364085A1
Processes for Preparing Phosphorodiamidate Morpholino Oligomers
Application: 16/302,018 →
Publication: US US20200080079A1
Processes for Preparing Phosphorodiamidate Morpholino Oligomers
Application: 16/302,529 →
Publication: US US20190292208A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 15/841,261 →
Publication: US US20180177814A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 17/736,148 →
Publication: US US20220280546A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 16/469,104 →
Publication: US US20210077628A2
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 16/001,310 →
Publication: US US20180271993A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 17/245,735 →
Publication: US US20210338830A1
Antisense Oligomer Compounds
Application: 16/754,805 →
Publication: US US20210130822A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 16/938,274 →
Publication: US US20210138078A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 16/938,278 →
Publication: US US20210138079A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 15/993,267 →
Publication: US US20190365918A1
Exon Skipping Oligomer Conjugates for Muscular Dystrophy
Application: 15/993,287 →
Publication: US US20190365919A1
Adeno-Associated Virus Antibodies, Fragments Thereof and Encoding Polynucleotides
Application: 17/478,645 →
Publication: US US20220033478A1
Systemic Delivery of Adeno-Associated Virus Vector Expressing Gamma-Sarcoglycan and the Treatment of Muscular Dystrophy
Application: 17/468,086 →
Publication: US US20220088123A1
Adeno-Associated Virus Vectors for Treatment of Rett Syndrome
Application: 17/406,723 →
Publication: US US20220056478A1
Related Assignments (24)
Other recorded transfers of the patents in this record — the chain of ownership.
Assignment of Assignor's Interest May 26, 2021
From: CAI, BAOZHONG; MARTINI, MITCHELL; SHIMABUKU, ROSS; THOMAS, KATIE
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 056355/0521 →
Assignment of Assignor's Interest Oct 6, 2023
From: HANSON, GUNNAR J.; ZHOU, MING
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 065148/0904 →
Assignment of Assignor's Interest Oct 10, 2024
From: PASSINI, MARCO A.; HANSON, GUNNAR J.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 068861/0823 →
Assignment of Assignor's Interest Oct 23, 2024
From: RAKHADE, SANJAY; CHARLESTON, JAY
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 069233/0545 →
Assignment of Assignor's Interest Jan 14, 2025
From: SUN, HUADONG; EAST, LILLY; TINSLEY, JON; ELKINS, JAKE
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 069865/0358 →
Assignment of Assignor's Interest Feb 7, 2025
From: CAI, BAOZHONG; MARTINI, MITCHELL; THOMAS, KATIE; SHIMABUKU, ROSS
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070154/0732 →
Assignment of Assignor's Interest Feb 13, 2025
From: SCHNELL, FREDERICK JOSEPH; PASSINI, MARCO; ESTRELLA, NELSA; HANSON, GUNNAR
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070206/0340 →
Assignment of Assignor's Interest Feb 26, 2025
From: BESTWICK, RICHARD K.; FRANK, DIANE ELIZABETH
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070331/0311 →
Change of Name Feb 26, 2025
From: AVI BIOPHARMA, INC.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070330/0604 →
Assignment of Assignor's Interest Feb 26, 2025
From: BESTWICK, RICHARD K.; FRANK, DIANE ELIZABETH; SCHNELL, FREDERICK JOSEPH
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070330/0378 →
Assignment of Assignor's Interest Feb 26, 2025
From: SAZANI, PETER; KOLE, RYSZARD
To: AVI BIOPHARMA, INC.
Reel/Frame 070330/0369 →
Assignment of Assignor's Interest Feb 27, 2025
From: PASSINI, MARCO A.; HANSON, GUNNAR J.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070353/0157 →
Assignment of Assignor's Interest Feb 27, 2025
From: SCHNELL, FREDERICK JOSEPH; WU, CHIA-LING
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070353/0242 →
Assignment of Assignor's Interest Mar 13, 2025
From: HANSON, GUNNAR J.; ZHOU, MING
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070499/0383 →
Assignment of Assignor's Interest Mar 14, 2025
From: SCHNELL, FREDERICK J.; CAI, BAOZHONG; GATLIN, JASON; IVERSEN, PATRICK L.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070523/0597 →
Assignment of Assignor's Interest Apr 2, 2025
From: SCHNELL, FREDERICK J.; CAI, BAOZHONG; GATLIN, JASON; IVERSEN, PATRICK L.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070718/0690 →
Assignment of Assignor's Interest Apr 7, 2025
From: SNEDEKER, JOHN; RODINO-KLAPAC, LOUISE; POTTER, RACHAEL
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070752/0655 →
Assignment of Assignor's Interest Apr 22, 2025
From: HANSON, GUNNAR J.; ZHOU, MING
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070919/0492 →
Assignment of Assignor's Interest Apr 22, 2025
From: LINSLEY, PETER; LEPPERT, BRIAN JAMES; HANSON, GUNNAR J.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 070905/0743 →
Assignment of Assignor's Interest May 27, 2025
From: KAYE, EDWARD M.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 071393/0386 →
Assignment of Assignor's Interest May 27, 2025
From: PASSINI, MARCO A.; HANSON, GUNNAR J
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 071393/0351 →
Assignment of Assignor's Interest May 27, 2025
From: PASSINI, MARCO A.; HANSON, GUNNAR J.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 071393/0347 →
Assignment of Assignor's Interest May 27, 2025
From: KAYE, EDWARD M.
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 071221/0437 →
Assignment of Assignor's Interest Feb 2, 2026
From: SCHNELL, FREDERICK JOSEPH
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 073653/0863 →