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DRUG:

BI 847325

i
Other names: BI 847325
Associations
Company:
Boehringer Ingelheim
Drug class:
MEK inhibitor, MEK1 inhibitor, MEK2 inhibitor, Aurora kinase A inhibitor, Aurora kinase inhibitor, Aurora kinase B inhibitor, Aurora kinase C inhibitor
Related drugs:
Associations
7ms
High in vitro and in vivo activity of BI-847325, a dual MEK/Aurora kinase inhibitor, in human solid and hematologic cancer models. (PubMed, Cancer Res Commun)
BI-847325 showed a broader range of activity than the MEK inhibitor GDC-0623. In conclusion, dual MEK/Aurora kinase inhibition shows remarkable potential for treating multiple types of hematological and solid tumors. The combination with capecitabine was synergistic in colorectal, gastric, and mammary cancer.
Preclinical • Journal
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BRAF (B-raf proto-oncogene) • NRAS (Neuroblastoma RAS viral oncogene homolog) • MAP2K1 (Mitogen-activated protein kinase kinase 1)
|
BRAF mutation • NRAS mutation
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capecitabine • BI 847325 • GDC-0623
over1year
BI-847325, a selective dual MEK and Aurora kinases inhibitor, reduces aggressive behavior of anaplastic thyroid carcinoma on an in vitro three-dimensional culture. (PubMed, Cancer Cell Int)
The results of the present study suggest that BI-857,325 might be an effective multi-targeted anticancer drug for ATC treatment.
Preclinical • Journal
|
ABCB1 (ATP Binding Cassette Subfamily B Member 1) • AURKA (Aurora kinase A) • AURKB (Aurora Kinase B) • ANXA5 (Annexin A5)
|
VEGFA expression
|
BI 847325
almost2years
GANT61/BI-847325 combination: a new hope in lung cancer treatment. (PubMed, Med Oncol)
To the best of our knowledge, the antitumor effects of BI-847325/GANT61 combination have not been tested before. Further in-vitro and in-vivo studies are warranted to support the findings.
Journal • IO biomarker
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mTOR (Mechanistic target of rapamycin kinase) • CCND1 (Cyclin D1) • MCL1 (Myeloid cell leukemia 1) • GLI1 (GLI Family Zinc Finger 1) • BAX (BCL2-associated X protein) • CASP3 (Caspase 3)
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BI 847325