Issued Patents All Time
Showing 1–25 of 26 patents
| Patent # | Title | Co-Inventors | Date |
|---|---|---|---|
| 12268755 | Allele-specific inactivation of mutant HTT via gene editing at coding region single nucleotide polymorphisms | Michael Harry Brodsky, Sarah Rinde Oikemus | 2025-04-08 |
| 12173286 | Fully stabilized asymmetric siRNA | Anastasia Khvorova, Julia Alterman, Matthew Hassler | 2024-12-24 |
| 12077755 | Bioactive conjugates for oligonucleotide delivery | Anastasia Khvorova, Mehran Nikan, Matthew Hassler, Maire Osborn, Reka Haraszti +2 more | 2024-09-03 |
| 12023407 | Artificial exosome composition and related methods | Reka Haraszti, Anastasia Khvorova | 2024-07-02 |
| 12024706 | Modified oligonucleotides targeting SNPs | Anastasia Khvorova, Julia Alterman, Faith Conroy, Edith Pfister, Ken Yamada | 2024-07-02 |
| 11827882 | Modified oligonucleotides targeting SNPs | Anastasia Khvorova, Julia Alterman, Faith Conroy, Edith Pfister, Ken Yamada | 2023-11-28 |
| 11773392 | AAV treatment of Huntington's disease | Christian Mueller, Edith Pfister | 2023-10-03 |
| 11753638 | Conjugated oligonucleotides | Anastasia Khvorova, Mehran Nikan, Matthew Hassler, Maire Osborn, Reka Haraszti +3 more | 2023-09-12 |
| 11505807 | Exosomal loading using hydrophobically modified oligonucleotides | Anastasia Khvorova, Marie Cecile Didiot, Reka Haraszti | 2022-11-22 |
| 11299734 | RNA interference for the treatment of gain-of-function disorders | Phillip D. Zamore | 2022-04-12 |
| 11230713 | Oligonucleotide compounds for targeting huntingtin mRNA | Anastasia Khvorova, Julia Alterman | 2022-01-25 |
| 11046957 | AAV treatment of Huntington's disease | Christian Mueller, Edith Pfister | 2021-06-29 |
| 10945955 | Artificial exosome composition and related methods | Reka Haraszti, Anastasia Khvorova | 2021-03-16 |
| 10774327 | Oligonucleotide compounds for targeting huntingtin mRNA | Anastasia Khvorova, Julia Alterman | 2020-09-15 |
| 10633653 | Bioactive conjugates for oligonucleotide delivery | Anastasia Khvorova, Mehran Nikan, Matthew Hassler, Maire Osborn, Reka Haraszti +2 more | 2020-04-28 |
| 10513710 | Exosomal loading using hydrophobically modified oligonucleotides | Anastasia Khvorova, Marie Cecile Didiot, Reka Haraszti | 2019-12-24 |
| 10457940 | AAV treatment of Huntington's disease | Christian Mueller, Edith Pfister | 2019-10-29 |
| 10435688 | Oligonucleotide compounds for targeting huntingtin mRNA | Anastasia Khvorova, Julia Alterman | 2019-10-08 |
| 10344277 | RNA interference for the treatment of gain-of-function disorders | Phillip D. Zamore | 2019-07-09 |
| 9914924 | Methods and compositions for treating neurological disease | Phillip D. Zamore | 2018-03-13 |
| 9809817 | Oligonucleotide compounds for targeting huntingtin mRNA | Anastasia Khvorova, Julia Alterman | 2017-11-07 |
| 9434943 | RNA interference for the treatment of gain-of-function disorders | Phillip D. Zamore | 2016-09-06 |
| 8987222 | Single nucleotide polymorphism (SNP) targeting therapies for the treatment of huntington'S disease | Edith Pfister, Phillip D. Zamore | 2015-03-24 |
| 8680063 | RNA interference for the treatment of gain-of-function disorders | Phillip D. Zamore | 2014-03-25 |
| 7947658 | RNA interference for the treatment of gain-of-function disorders | Phillip D. Zamore | 2011-05-24 |