Berlin
Germany
20
2026-02-05
The entities that hold a legal rights for patent applications filed by inventor Korr Daniel:
Daniel Korr from Berlin, DE has applied for patents for these inventions. The list has both pending applications and granted patents:
1H-PYRROLO[3,2-B]PYRIDINE DERIVATIVES AS IRREVERSIBLE INHIBITORS OF MUTANT EGFR FOR THE TREATMENT OF CANCER
#2 | 2025-05-014H-PYRROLO[3,2-C]PYRIDIN-4-ONE COMPOUNDS
#3 | 2024-09-194H-PYRROLO[3,2-c]PYRIDIN-4-ONE COMPOUNDS
#4 | 2024-08-29SUBSTITUTED ACYL SULFONAMIDES FOR TREATING CANCER
#5 | 2024-08-22SUBSTITUTED ACYL SULFONAMIDES FOR TREATING CANCER
#6 | 2023-12-28N-[2-({4-[3-(ANILINO)-4-OXO-4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-2-YL]PYRIDIN-3-YL)OXY)ETHYL]PROP-2-ENAMIDE DERIVATIVES AND SIMILAR COMPOUNDS AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER
#7 | 2023-03-023-(ANILINO)-2-[3-(3-ALKOXY-PYRIDIN-4-YL]-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER
#8 | 2022-12-014H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES
#9 | 2022-09-224H-PYRROLO[3,2-C]PYRIDIN-4-ONE COMPOUNDS
#10 | 2022-07-21ACYL SULFONAMIDES FOR TREATING CANCER
#11 | 2022-05-244H-pyrrolo[3,2-c]pyridin-4-one derivatives
#12 | 2020-04-23THIAZOLE COMPOUNDS USEFUL AS PRMT5 INHIBITORS
#13 | 2015-02-05Heterocyclyl aminoimidazopyridazines
#14 | 2014-09-25AMINO-SUBSTITUTED IMIDAZOPYRIDAZINES AS MKNK1 KINASE INHIBITORS
#15 | 2014-07-10Substituted aminoimidazopyridazines
#16 | 2009-01-29PROGESTERONE-RECEPTOR ANTAGONIST FOR USE IN BRCA ALONE OR AS COMBINATION WITH ANTIESTROGEN
#17 | 2008-12-18USE OF FIBROBLAST GROWTH FACTOR 7 (Fgf7) AND OF THE RECEPTOR Fgfr2b AS BIOMARKERS
#18 | 2008-10-30COMBINATION OF PROGESTERONE-RECEPTOR ANTAGONIST TOGETHER WITH NONE-STEROIDAL ANTIESTROGEN FOR USE IN BRCA MEDIATED DISEASES
#19 | 2008-10-23COMBINATION OF PROGESTERONE-RECEPTOR ANTAGONIST TOGETHER WITH A LUTEIN-HORMONE-RELEASING HORMONE AGONIST AND ANTAGONIST FOR USE IN BRCA MEDIATED DISEASES
#20 | 2008-10-23COMBINATION OF PROGESTERONE-RECEPTOR ANTAGONIST TOGETHER WITH AN AROMATASE INHIBITOR FOR USE IN BRCA MEDIATED DISEASES
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