Patents by Inventor Christoph Lengauer
Christoph Lengauer has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Patent number: 10875930Abstract: The invention provides to PIK3C2G (phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 gamma) gene fusions and PIK3C2G fusion proteins. The invention further provides methods of diagnosing and treating diseases or disorders associated with PK3C2G fusions, such as conditions mediated by aberrant PIK3C2G expression or activity, or conditions associated with overexpression of PIK.3C2G.Type: GrantFiled: July 30, 2014Date of Patent: December 29, 2020Assignee: BLUEPRINT MEDICINES CORPORATIONInventors: Nicolas Stransky, Ethan G. Cerami, Joseph L. Kim, Christoph Lengauer
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Patent number: 10669590Abstract: The invention provides PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha) gene fusions, and fragments of those gene fusions. The invention further provides methods of diagnosing and treating diseases or disorders associated with PIK3CA fusions, such as conditions mediated by PIK3CA aberrant expression or activity, or overexpression of PIK3CA.Type: GrantFiled: February 27, 2019Date of Patent: June 2, 2020Assignee: Blueprint Medicines CorporationInventors: Ethan G. Cerami, Christoph Lengauer, Nicolas Stransky
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Publication number: 20190389969Abstract: The invention provides to NTRK (“Neurotrophic Tyrosine Receptor Kinase) gene fusions, NTRK. fosion proteins, and fragments of those genes and polypeptides.Type: ApplicationFiled: August 1, 2019Publication date: December 26, 2019Applicant: Blueprint Medicines CorporationInventors: Nicolas STRANSKY, Ethan G. CERAMI, Christoph LENGAUER
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Patent number: 10407509Abstract: The invention provides to NTRK (“Neurotrophic Tyrosine Receptor Kinase) gene fusions, NTRK, fusion proteins, and fragments of those genes and polypeptides. The invention further provides methods of diagnosing and treating diseases or disorders associated with NTRK fusions, such as conditions mediated by aberrant NTRK expression or activity, or overexpression of NTRK.Type: GrantFiled: July 30, 2014Date of Patent: September 10, 2019Assignee: Blueprint Medicines CorporationInventors: Nicolas Stransky, Ethan G. Cerami, Christoph Lengauer
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Publication number: 20190192522Abstract: Described herein are selective inhibitors of FGFR4, pharmaceutical compositions including such compounds, and combinations with other therapeutic agents, such as CDK inhibitors (e.g., CDK4/6 inhibitors), and methods of using such combinations.Type: ApplicationFiled: September 8, 2017Publication date: June 27, 2019Applicant: BLUEPRINT MEDICINES CORPORATIONInventors: Margit HAGEL, Klaus HOEFLICH, Christoph LENGAUER, Nicolas STRANSKY, Christopher WINTER, Lan XU
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Publication number: 20190185942Abstract: The invention provides PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha) gene fusions, and fragments of those gene fusions. The invention further provides methods of diagnosing and treating diseases or disorders associated with PIK3CA fusions, such as conditions mediated by PIK3CA aberrant expression or activity, or overexpression of PIK3CA.Type: ApplicationFiled: February 27, 2019Publication date: June 20, 2019Applicant: BLUEPRINT MEDICINES CORPORATIONInventors: Ethan G. Cerami, Christoph Lengauer, Nicolas Stransky
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Publication number: 20170044621Abstract: The invention provides MET gene fusions. MET fusion proteins, and fragments of those genes and polypeptides. The invention further provides methods of diagnosing and treating diseases or disorders associated with MET fusions, such as conditions mediated by aberrant MET expression or activity or overexpression of MET.Type: ApplicationFiled: April 17, 2015Publication date: February 16, 2017Applicant: BLUEPRINT MEDICINES CORPORATIONInventors: Ehan G. Cerami, Christoph Lengauer, Nicolas Stransky
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Publication number: 20170044622Abstract: The invention provides PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) gene fusions, and fragments of those gene fusions. The invention further provides methods of diagnosing and treating diseases or disorders associated with PIK3CA fusions, such as conditions mediated by PIK3CA aberrant expression or activity, or overexpression of PIK3CA.Type: ApplicationFiled: April 17, 2015Publication date: February 16, 2017Applicant: BLUEPRINT MEDICINES CORPORATIONInventors: Ethan G. Cerami, Christoph Lengauer, Nicolas Stransky
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Publication number: 20160272725Abstract: The invention provides to NTRK (“Neurotrophic Tyrosine Receptor Kinase) gene fusions, NTRK. fusion proteins, and fragments of those genes and polypeptides. The invention further provides methods of diagnosing and treating diseases or disorders associated with NTRK fusions, such as conditions mediated by aberrant NTRK expression or activity, or overexpression of NTRK.Type: ApplicationFiled: July 30, 2014Publication date: September 22, 2016Inventors: Nicolas STRANSKY, Ethan G. CERAMI, Christoph LENGAUER
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Publication number: 20160251446Abstract: The invention provides to PIK3C2G (phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 gamma) gene fusions and PIK3C2G fusion proteins. The invention further provides methods of diagnosing and treating diseases or disorders associated with PK3C2G fusions, such as conditions mediated by aberrant PIK3C2G expression or activity, or conditions associated with overexpression of PIK.3C2G.Type: ApplicationFiled: July 30, 2014Publication date: September 1, 2016Inventors: Nicolas STRANSKY, Ethan G. CERAMI, Joseph L. KIM, Christoph LENGAUER
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Patent number: 7354703Abstract: Securin-deficient cells and their isogenic securin-proficient counterparts are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to preferentially inhibit or kill a securin-deficient cell. The association of securin deficiency and chromosomal instability leading to aneuploidy, renders securin an excellent target for chemotherapeutic drug development.Type: GrantFiled: March 23, 2001Date of Patent: April 8, 2008Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Kenneth W. Kinzler, Prasad Jallepalli, Christoph Lengauer
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Patent number: 7148009Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: GrantFiled: December 17, 2002Date of Patent: December 12, 2006Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Publication number: 20050202465Abstract: Thymidylate synthase (TYMS) gene amplification was observed in 23% of 31 5-FU resistant liver metastases, while no amplification was observed in metastases of patients that had not been treated with 5-FU. Patients with metastases containing TYMS amplification had a substantially shorter median survival (329 days) than those without amplification (1021 days, p<0.01). Genetic amplification of TYMS has important implications for the management of colorectal cancer patients with recurrent disease.Type: ApplicationFiled: November 24, 2004Publication date: September 15, 2005Applicant: The Johns Hopkins UniversityInventors: Tian-Li Wang, Luis Diaz, Christoph Lengauer, Victor Velculescu, Kenneth Kinzler, Bert Vogelstein
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Publication number: 20030108941Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: ApplicationFiled: December 17, 2002Publication date: June 12, 2003Applicant: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Patent number: 6511818Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: GrantFiled: April 10, 2001Date of Patent: January 28, 2003Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Publication number: 20020137018Abstract: Securin-deficient cells and their isogenic securin-proficient counterparts are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to preferentially inhibit or kill a securin-deficient cell. The association of securin deficiency and chromosomal instability leading to aneuploidy, renders securin an excellent target for chemotherapeutic drug development.Type: ApplicationFiled: March 23, 2001Publication date: September 26, 2002Inventors: Bert Vogelstein, Kenneth W. Kinzler, Prasad Jallepalli, Christoph Lengauer
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Publication number: 20010012619Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: ApplicationFiled: April 10, 2001Publication date: August 9, 2001Inventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Patent number: 5888735Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: GrantFiled: January 10, 1997Date of Patent: March 30, 1999Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Patent number: 5882865Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: GrantFiled: January 10, 1997Date of Patent: March 16, 1999Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler
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Patent number: 5879889Abstract: Checkpoint gene-defective human cells are useful for screening potential anti-tumor agents. Potential therapeutic agents are screened for the ability to cause DNA accumulation or cell death in a checkpoint gene-defective human cell.Type: GrantFiled: January 10, 1997Date of Patent: March 9, 1999Assignee: The Johns Hopkins UniversityInventors: Bert Vogelstein, Todd Waldman, Christoph Lengauer, Kenneth W. Kinzler