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XENON PHARMACEUTICALS INC. (NASDAQ:XENE) Files An 8-K Results of Operations and Financial Condition

XENON PHARMACEUTICALS INC. (NASDAQ:XENE) Files An 8-K Results of Operations and Financial ConditionItem 2.02

Results of Operations and Financial Condition

On November 7, 2017, Xenon Pharmaceuticals Inc. (the “Company”) announced via press release the Company’s financial results for the nine month period ended September 30, 2017.A copy of the Company’s press release is attached hereto as Exhibit 99.1.The information in this Form8‑K and the attached exhibit are furnished to, but not filed with, the Securities and Exchange Commission.

Item 2.02

Financial Statements and Exhibits

(d) Exhibits.

to the rules and regulations of the Securities and Exchange Commission, the attached exhibit is deemed to have been furnished to, but not filed with, the Securities and Exchange Commission:

Xenon Pharmaceuticals Inc. ExhibitEX-99.1 2 xene-ex991_6.htm EX-99.1 xene-ex991_6.htm EXHIBIT 99.1 NEWS RELEASE   Xenon Pharmaceuticals Reports Third Quarter 2017 Financial Results and Provides Corporate Update   BURNABY,…To view the full exhibit click here
About XENON PHARMACEUTICALS INC. (NASDAQ:XENE)
Xenon Pharmaceuticals Inc. (Xenon) is a biopharmaceutical company discovering and developing a pipeline of differentiated therapeutics for orphan indications. The Company’s platform, Extreme Genetics, enables the discovery of validated drug targets by studying rare human diseases with extreme traits, including diseases caused by mutations in ion channels (channelopathies). Extreme Genetics involves the study of families where individuals exhibit inherited severe traits, or phenotypes. Its integrated platform includes in-house capabilities for human genetics, small molecule drug discovery, as well as preclinical and clinical development. Its pharmaceutical partners include Teva Pharmaceutical Industries, Ltd. (Teva), Genentech, Inc. (Genentech) and Merck & Co., Inc. (Merck). Extreme Genetics discovery platform has yielded the first approved gene therapy product in the European Union, or the EU, and a development pipeline, including Glybera, TV-45070, GDC-0276 and GDC-0310, and XEN801.

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