Alectinib

Alectinib
Systematic (IUPAC) name
9-Ethyl-6,6-dimethyl-8-[4-(4-morpholinyl)-1-piperidinyl]-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile
Clinical data
Trade names Alecensa
AHFS/Drugs.com Multum Consumer Information
Legal status
Identifiers
CAS Number 1256580-46-7
ATC code None
PubChem CID 49806720
DrugBank DB11363
ChemSpider 26326738
KEGG D10542
ChEBI CHEBI:90936
Chemical data
Formula C30H34N4O2
Molar mass 482.62 g/mol

Alectinib (marketed as Alecensa) is an oral drug that blocks the activity of anaplastic lymphoma kinase (ALK)[1][1][2] and is used to treat non-small cell lung cancer (NSCLC). It was developed by Chugai Pharmaceutical Co. Japan, which is part of the Hoffmann-La Roche group.

Approvals and indications

Approved in Japan in July 2014[3] for the treatment of ALK fusion-gene positive, unresectable, advanced or recurrent non-small cell lung cancer.[2]

Alecensa was approved by the US FDA in December 2015 to treat patients with advanced ALK-positive NSCLC whose disease worsened after, or who could not tolerate, treatment with crizotinib (Xalkori).[1]

Clinical trials

In a Japanese trial, after approximately 2 years, 19.6% of patients had achieved a complete response, and the 2-year progression-free survival rate is 76%.[2]

In Feb 2016 the J-ALEX phase III study comparing alectinib with crizotinib was terminated early because an interim anaysis showed that progression-free survival was longer with alectinib.[4]

References

External links


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