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CRISPR Therapeutics AG Patents

What CRISPR Therapeutics AG has filed at the patent office — applications as well as grants, because a filing is on the record eighteen months before anyone has to say what it was for.

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Filings on file
31
Granted
1
Still pending
30
Filed under
2 names

31 filings

Newest filing first. A pending application has no patent number yet, and most never get one.

InventionPatent
UNIVERSAL DONOR CELLSA61K 35/39, C12N 5/0678, C12N 15/85, A61P 3/10, A61K 35/12, A61K 35/28, A61K 35/545, A61K 38/1709, C07K 14/70539, C07K2319/02, C07K2319/03, C12N 5/0606, C12N 5/0607, C12N 5/0696, C12N 5/10, C12N 5/16, C12N2506/02, C12N2506/45, C12N2510/00Filed as CRISPR Therapeutics AG2025-08-18Alireza Rezaniapending
RT EDITING COMPOSITIONS AND METHODSA61K 48/005, C12Y 207/07049, C12N2310/20, A61P 5/00, A61P 11/00, A61K 9/1272, A61K 9/5123, C07K2319/09, C07K2319/80, C12N 9/1276, C12N 9/22, C12N 15/00, C12N 15/111, C12N 15/1137, C12N 15/86, C12N 15/88, C12N2320/34, C12N2750/14143, C12N2800/22, C12N2830/48Filed as CRISPR Therapeutics AG2025-02-26Christof Fellmannpending
GENETICALLY ENGINEERED T CELLS WITH REGNASE-1 AND/OR TGFBRII DISRUPTION HAVE IMPROVED FUNCTIONALITY AND PERSISTENCEC07K 14/70578, C12N 5/0636, C12N2310/20, A61K2239/48, A61K2239/31, A61K2239/56, A61K2239/38, A61K2239/54, A61K 40/4232, A61K 40/4251, A61K 40/4215, A61K 40/4211, A61K 40/31, A61K 40/50, A61K 40/11, C12N 9/226, A61K 38/00, A61K 48/00, C07K 14/7051, C07K 14/70521, C07K 14/70575, C07K 14/70596, C07K 14/71, C07K 16/2803, C07K 16/2875, C07K 16/2878, C07K 16/30, C07K2317/622, C07K2319/02, C07K2319/03, C12N 5/16, C12N 9/22, C12N 15/111, C12N 15/113, C12N 15/1138, C12N 15/86, C12N 15/907, C12N2310/315, C12N2310/321, C12N2310/3521, C12N2510/00, C12N2750/14143Filed as CRISPR Therapeutics AG2025-02-18Mary-Lee Dequeantpending
GENE-EDITED NATURAL KILLER CELLSA61K 35/17, C12N 5/0646, A61P 35/00, A61K2239/55, A61K 40/4202, A61K 40/15, A61K 40/31, C07K 14/5443, C07K 14/7051, C07K 14/7155, C12N2510/00Filed as CRISPR Therapeutics AG2025-01-30Alireza Rezaniapending
METHODS AND COMPOSITIONS FOR TREATING CANCERC07K 16/2878, C12N 5/0636, C12N2310/20, A61K 47/6849, A61P 35/00, A61K2039/86, A61K2039/852, A61K2039/892, A61K2039/868, A61K2039/804, A61K2239/28, A61K2239/31, A61K2239/38, A61K 40/4232, A61K 40/4215, A61K 40/4211, A61K 40/32, A61K 40/31, A61K 40/50, A61K 40/421, A61K 40/11, C12N 9/226, A61K 35/17, A61K 38/00, A61K 51/1027, A61K2039/505, A61K2039/5156, A61K2121/00, A61K2300/00, C07K 14/7051, C07K 14/70517, C07K 14/70521, C07K 14/70539, C07K 14/70578, C07K 16/2803, C07K 16/2875, C07K2317/565, C07K2317/622, C07K2317/74, C07K2317/76, C07K2319/02, C07K2319/03, C07K2319/30, C07K2319/33, C12N 9/22, C12N 15/11, C12N 15/86, C12N2510/00, C12N2750/14143, C12N2800/80Filed as CRISPR Therapeutics AG2025-01-14Jonathan Alexander Terrettpending
MATERIALS AND METHODS FOR TREATMENT OF HEREDITARY HAEMOCHROMATOSISA61K 48/0058, C12N 15/102, C12N2310/20, C12N 9/224, A61K 9/0019, A61K 48/005, A61K 48/0066, A61K 48/0075, C12N 5/0663, C12N 5/067, C12N 15/1138, C12N 15/907Filed as CRISPR Therapeutics AG2025-01-05Roman Lvovitch Bogoradpending
MESSENGER RNA ENCODING CAS9 FOR USE IN GENOME-EDITING SYSTEMSC12N 9/226, C12N 15/111, C12N2310/20, A61K 9/5123, A61K 31/7088, A61K 48/00, A61K 48/005, C12N 9/22, C12N 15/102, C12N 15/11, C12N 15/88, C12N 15/907, C12N2310/335, C12N2320/32, C12N2800/80Filed as CRISPR THERAPEUTICS AG2025-01-03Christian Cobaughpending
BASE EDITING PROTEINS AND USES THEREOFC12N 9/226, C12N 9/22, C12N2310/20, A61P 35/00, A61K 40/4232, A61K 40/4224, A61K 40/31, A61K 40/11, A61K 31/7105, A61K 38/465, A61K 38/50, A61K2039/505, A61K2039/5156, C07K 16/2875, C07K2319/00, C07K2319/03, C07K2319/09, C07K2319/33, C07K2319/70, C12N 5/0636, C12N 9/78, C12N 15/11, C12N 15/113, C12N 15/62, C12N 15/907, C12N2510/00, C12Y 305/04005Filed as CRISPR THERAPEUTICS AG2024-12-19John KULMANpending
METHODS AND COMPOSITIONS FOR IN VIVO EDITING OF STEM CELLSA61K 48/0058, C12N 15/86, C12N2310/20, C12N 9/226, C12N 5/0647, C12N 15/102, C12N 15/11, C12N 15/113, C12N 15/1138, C12N 15/907, C12N2510/00, C12N2750/14143, C12N2800/40Filed as CRISPR THERAPEUTICS AG2024-12-19Kyungah MAENGpending
CHIMERIC ANTIGEN RECEPTOR SPECIFIC TO CD117A61K 40/31, C07K 16/2803, A61P 35/00, A61K2239/13, A61K 40/4216, A61K 40/4215, A61K 40/11, A61K 35/14, A61K2039/5156, C07K 14/7051, C07K 14/70517, C07K 14/70521, C07K 14/70575, C07K2317/22, C07K2317/565, C07K2317/569, C07K2317/622, C07K2317/73, C07K2319/02, C07K2319/03, C07K2319/33, C12N 5/0634, C12N 5/10, C12N 15/625, C12N2510/00Filed as CRISPR THERAPEUTICS AG2024-12-19Jason SAGERTpending
CD117-TARGETING NANOPARTICLES FOR USE IN DRUG DELIVERYA61K 47/6913, C07K 16/2803, C12N2310/20, A61K 47/6849, C12N 9/222, C07K2317/33, C07K2317/35, C07K2317/40, C07K2317/565, C07K2317/567, C07K2317/569, C07K2317/77, C07K2317/92, C07K2317/94, C07K2319/01, C07K2319/02, C07K2319/21, C12N 15/11, C12N 15/111, C12N 15/88, C12N2320/32Filed as CRISPR THERAPEUTICS AG2024-12-19Megan D. WARNERpending
CHIMERIC ANTIGEN RECEPTOR TARGETING GPC-3 AND IMMUNE CELLS EXPRESSING SUCH FOR THERAPEUTIC USESA61K 35/17, C07K 16/303, A61P 35/00, A61K2239/13, A61K2239/53, A61K2239/21, A61K2239/22, A61K 40/4261, A61K 40/4202, A61K 40/31, A61K 40/11, C12N 9/226, C07K 14/7051, C07K 14/70517, C07K 14/70521, C07K 14/70539, C07K 14/70578, C07K 14/71, C07K 14/82, C07K2317/565, C07K2317/569, C07K2319/00, C07K2319/03, C07K2319/33, C12N 5/0636, C12N 9/104, C12N 9/22, C12N2510/00, C12Y 203/02Filed as CRISPR THERAPEUTICS AG2024-12-06Jason Sagertpending
GENE-EDITED NATURAL KILLER CELLSC12N 5/0646, C12N2310/20, A61P 35/00, A61K2239/55, A61K2239/53, A61K2239/31, A61K 40/35, A61K 40/13, A61K 40/4261, A61K 40/30, A61K 40/42, A61K 40/4202, A61K 40/15, A61K 40/31, A61K 40/50, A61K 40/11, A61K 9/0019, A61K 35/17, C07K 14/5443, C07K 14/7051, C07K 14/70535, C07K 14/70539, C07K 14/70596, C07K 14/7155, C07K 14/8121, C07K2319/00, C12N 5/0606, C12N 5/0635, C12N 5/0636, C12N 5/0647, C12N 5/0696, C12N 9/22, C12N 15/1138, C12N 15/62, C12N 15/63, C12N2506/45, C12N2510/00Filed as CRISPR THERAPEUTICS AG2024-11-30Valentin SLUCHpending
COMPOSITIONS AND METHODS FOR DIFFERENTIATING STEM CELLS INTO NK CELLSC12N 5/0646, C12N 5/0696, A61K 35/17, C12N2501/115, C12N2501/125, C12N2501/145, C12N2501/155, C12N2501/16, C12N2501/165, C12N2501/2303, C12N2501/2307, C12N2501/2315, C12N2501/26, C12N2501/415, C12N2501/727, C12N2506/00, C12N2506/02, C12N2506/03, C12N2506/45, C12N2510/00Filed as CRISPR THERAPEUTICS AG2024-11-30Viktoriia KYRYCHENKOpending
ANTI-PTK7 IMMUNE CELL CANCER THERAPYC07K 14/70521, C07K 16/40, C12N 5/0636, A61P 35/00, A61K2039/86, A61K2039/852, A61K2039/892, A61K2239/55, A61K2239/59, A61K2239/49, A61K2239/38, A61K2239/54, A61K 40/4251, A61K 40/4211, A61K 40/31, A61K 40/11, A61K 35/17, A61K2039/505, A61K2121/00, A61K2300/00, C07K 14/7051, C07K 14/70539, C07K 14/70575, C07K 14/70578, C07K2317/56, C07K2317/565, C07K2317/622, C07K2319/00, C07K2319/02, C07K2319/03, C12N 15/11, C12N 15/86, C12N2510/00, C12N2750/14143Filed as CRISPR THERAPEUTICS AG2024-11-14Jonathan Alexander Terrettpending
RT EDITING COMPOSITIONS AND METHODSFiled as CRISPR Therapeutics AG2024-11-11Christof Fellmannpending
GUIDE DESIGN AND OFF-TARGET SEARCHESG16B 30/10, C12N2310/20, C12N 9/226, C12N 15/11, C12N 15/907, G16B 35/10Filed as CRISPR THERAPEUTICS AG2024-10-25John Michael TOOMEYpending
METHODS AND COMPOSITIONS FOR TREATING LIPOPROTEIN-RELATED DISEASESA61K 38/465, C12N 15/113, C12N2310/20, A61P 9/00, C12N 9/226, A61K 9/5123, A61K 31/7088, A61K 38/00, A61K 48/0058, C12N 15/11, C12N 15/111, C12N 15/907Filed as CRISPR THERAPEUTICS AG2024-09-20Sanjay D'SOUZApending
METHODS AND COMPOSITIONS FOR TREATING LIPOPROTEIN-RELATED DISEASESA61K 38/465, C12N 15/113, C12N2310/20, A61P 9/00, C12N 9/226, A61K 9/5123, A61K 31/7088, A61K 38/00, A61K 48/0058, C12N 15/11, C12N 15/111, C12N 15/907Filed as CRISPR THERAPEUTICS AG2024-09-20Sanjay D'SOUZApending
METHODS AND COMPOSITIONS FOR TREATING LIPOPROTEIN-RELATED DISEASESA61K 38/465, C12N 15/113, C12N2310/20, A61P 9/00, C12N 9/226, A61K 9/5123, A61K 31/7088, A61K 38/00, A61K 48/0058, C12N 15/11, C12N 15/111, C12N 15/907Filed as CRISPR THERAPEUTICS AG2024-09-20Sanjay D'SOUZApending
MODULATING EXPRESSION OF ALAS1 (5'-AMINOLEVULINATE SYNTHASE 1) GENEC12N 15/1137, C12N2310/20, C12N 9/226, C12N 15/88, C12N2310/315, C12N2310/321, C12Y 203/01037Filed as CRISPR Therapeutics AG2024-07-21Mary-Lee Dequeant12644123
METHODS AND COMPOSITIONS FOR TREATING ANGIOPOIETIN-LIKE 3 (ANGPTL3) RELATED CONDITIONSC12N 9/226, C12N 15/113, C12N2310/20, A61P 3/00, C12N 15/11Filed as CRISPR Therapeutics AG2024-07-11Yi-Shan Chenpending
METHODS AND COMPOSITIONS FOR TREATING ANGIOPOIETIN-LIKE 3 (ANGPTL3) RELATED CONDITIONSC12N 9/226, C12N 15/113, C12N2310/20, A61P 3/00, C12N 15/11Filed as CRISPR Therapeutics AG2024-07-11Yi-Shan Chenpending
RT EDITING COMPOSITIONS AND METHODSFiled as CRISPR Therapeutics AG2024-05-20Christof Fellmannpending
COMPOSITIONS AND METHODS FOR THE DEPLETION OF CD117+ CELLSC07K 16/2896, A61K 47/6831, A61K 47/6817, A61K 47/6849, A61P 37/06, A61P 35/00, A61K 35/545, A61K 38/00, A61K2035/124, A61K2039/505, C07K 7/64, C07K 16/2803, C07K2317/21, C07K2317/52, C07K2317/55, C07K2317/71, C07K2317/73, C07K2317/92, C07K2317/94Filed as CRISPR THERAPEUTICS AG2024-04-04Bradley R. Pearsepending
MASKED CHIMERIC ANTIGEN RECEPTOR SPECIFIC TO TYROSINE-PROTEIN KINASE LIKE 7 (PTK7) AND IMMUNE CELLS EXPRESSING SUCHC07K 14/705, C07K 16/40, A61P 35/00, A61K2239/31, A61K2239/38, A61K2239/54, A61K 40/4251, A61K 40/31, A61K 40/11, A61K 35/17, A61K 38/00, A61K2039/505, A61K2039/5156, A61K2039/5158, C07K 7/08, C07K 14/47, C07K 14/7051, C07K 14/70517, C07K 14/70521, C07K 14/70578, C07K 16/3046, C07K2317/622, C07K2317/72, C07K2317/73, C07K2317/76, C07K2317/92, C07K2319/02, C07K2319/03, C07K2319/30, C07K2319/33, C07K2319/50, C12N 5/0636, C12N 15/62, C12N2510/00, C12Y 207/01112Filed as CRISPR Therapeutics AG2024-03-04Jason Sagertpending
RT EDITING COMPOSITIONS AND METHODSFiled as CRISPR Therapeutics AG2024-02-27Christof Fellmannpending
COMPOSITIONS AND METHODS FOR GENE EDITINGC12N 15/111, C12N 15/86, C12N2310/20, C12N 9/226, C07K 14/515, C12N 7/00, C12N 9/22, C12N 15/1136, C12N2750/14143, C12N2800/80Filed as CRISPR THERAPEUTICS AG2024-02-16Ante Sven Lundbergpending
GENE-EDITED NATURAL KILLER CELLSFiled as CRISPR Therapeutics AG2024-01-31Alireza Rezaniapending
MODULATING EXPRESSION OF ALAS1 (5'-AMINOLEVULINATE SYNTHASE 1) GENEFiled as CRISPR Therapeutics AG2024-01-24Mary-Lee Dequeantpending
MATERIALS AND METHODS FOR TREATMENT OF GLYCOGEN STORAGE DISEASE TYPE 1AC12N 15/102, C12N 15/907, C12N2310/20, C12N 9/226, A61K 38/00, C12N 9/16, C12N 15/11, C12N2800/80, C12Y 301/03009Filed as CRISPR THERAPEUTICS AG2024-01-08Chad Albert COWANpending

Filings are matched to the company by applicant name, so a subsidiary filing under its own name is only here if that name resolves to this company. The applicant is printed as filed, which makes a wrong match visible. A patent is not a product: most applications are never granted, and most grants are never built.

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