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filingDate 2014-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-102304108-B1
titleOfInvention Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for treating lymphomas
abstract - non-Hodgkin's lymphoma (NHL), in particular primary, secondary, relapsed, refractory, delayed or aggressive non-Hodgkin's lymphoma (NHL), in particular follicular lymphoma (FL), chronic lymphocytic leukemia (CLL) , for the manufacture of a medicament for the treatment or prophylaxis of marginal zone lymphoma (MZL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL), metamorphic lymphoma (TL), or peripheral T-cell lymphoma (PTCL) , a 2,3-dihydroimidazo[1,2-c]quinazoline compound, or a pharmaceutical composition comprising it as the sole active agent, or a) said compound or a pharmaceutical composition comprising said compound and b) one or more additional use of combinations of active agents; n n n - a) a combination of said compound with b) at least one further active agent; - non-Hodgkin's lymphoma (NHL), in particular primary, secondary, relapsed, refractory, delayed or aggressive non-Hodgkin's lymphoma (NHL), in particular follicular lymphoma (FL), chronic lymphocytic leukemia (CLL) , marginal zone lymphoma (MZL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL), metamorphic lymphoma (TL), or peripheral T-cell lymphoma (PTCL) as the only active agent. pharmaceutical compositions that - a pharmaceutical composition comprising a combination of a) said compound and b) at least one further active agent; - expression of PI3K isoforms, BTK and IKK, BCR, for predicting sensitivity and/or resistance to said compounds in cancer patients and providing an evidence-based synergistic combination as defined herein for increasing sensitivity and/or overcoming resistance use of biomarkers involved in activation, activation of BCR downstream of the NFκB pathway, alteration of c-Myc, EZH2; and - a method for determining the level of one or more components of the PI3K isoform, expression of BTK and IKK, BCR activation, BCR downstream activation of the NFκB pathway, c-Myc, EZH2.
priorityDate 2013-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID476828
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID557176
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426359782
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413276852
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID170911
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5394
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413276829
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Total number of triples: 1336.