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MEK162 Registration Path Announced
Date:11/8/2012

BOULDER, Colo., Nov. 8, 2012 /PRNewswire/ -- At its R&D Investor event earlier today, Novartis provided an update on the clinical development strategy for MEK162 (ARRY-162).  Novartis intends to initiate pivotal trials in patients with NRAS mutant melanoma during 2013, with the goal of regulatory submissions on or after 2016.  In addition, Novartis announced plans to pursue clinical development in combination with a Raf inhibitor, in BRAF mutant melanoma, with regulatory submissions forecast for on or after 2016.  To listen to the webcast or view the slides from the R&D Investor event, please click here:  http://www.novartis.com/investors/event-calendar/index.shtml#2012-11-08_investor

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"We are pleased that Novartis is expected to advance MEK162 into pivotal trials next year," said Ron Squarer, Chief Executive Officer, Array BioPharma.  "Based on the positive Phase 2 trial results in NRAS mutant melanoma, MEK162 may provide a new option for patients with particularly poor prognoses.  We are also excited that Novartis is building on their positive trial results in patients with BRAF melanoma to pursue an additional clinical program in this population."

Array BioPharma Inc. (NASDAQ: ARRY) invented MEK162 and licensed worldwide rights to develop and commercialize MEK162 to Novartis in April 2010.  As part of the agreement, Array is co-developing MEK162 with Novartis and retains an option to co-detail the product in the US.

MEK162 Phase 2 BRAF/NRAS Phase 2 Trial Results
The ongoing Phase 2 open-label trial with MEK162 as a single agent is being conducted by Novartis and continues to enroll patients.  As reported at ASCO, the disease control rate (partial r
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SOURCE Array BioPharma Inc.
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