Also mentioned was the PROC trial with VTX2337, the lead compound for VentiRx. The PR notes that the compound is partnered with CELG and not with ARRY. I need to read up on what the terms are.
Being more familiar with the ONXX side rather than the ARRY side, these are the points to come to mind:
For: It would be consistent for ONXX because they've been rather aggressive with carfilzomib. I think ONXX believes they have an inherent edge versus velcade and they're already embarked on that journey, so a combo with a novel drug may be a first shot at competing against revlimid.
For: I'm a broken record on this, but ONXX's preclinical work is not the envy of the biotech sector, so trying to leverage their cash flow with a few novel shots on goal would make sense for them.
For: Monotherapy is the easiest (and arguably most reliable) way to market for multiple myeloma. If ARRY is trying to hedge their bets then it would be a good fit.
Against: As an ONXX shareholder, I would not be in favour of an in-licensing. Due to point #3, I think that ARRY is showing their hand and I would use that as leverage. Maybe provide some free drug and help a little bit with trial costs, but not much more.
Array BioPharma To Present Clinical Data On ARRY-797 At The 2012 American College Of Rheumatology Annual Meeting
BOULDER, Colo., Nov. 6, 2012 /PRNewswire/ -- Array BioPharma Inc. (ARRY) announced that an abstract discussing the final Phase 2 trial results with ARRY-797 in patients with osteoarthritis pain will be presented at the 2012 American College of Rheumatology Annual Meeting in Washington, D.C. This abstract includes data on ARRY-797's analgesic effect and markers of disease modification. In addition, biomarkers of cartilage (COMP) and bone (CTX-I) degradation were assessed. ARRY-797 treatment resulted in statistically significant decreases in COMP and CTX-I at week 4 (decreases of 10% and 38% versus placebo, respectively). The decrease in CTX-I was sustained and returned to baseline by the follow-up visit. The abstract concludes that further evaluation of the potential for disease modifying activity is warranted.
The abstract can be accessed through the American College of Rheumatology Annual Meeting website, http://www.rheumatology.org/apps/MyAnnualMeeting/ExploreMeeting. After the presentation, the poster will be available as a PDF on Array's website at www.arraybiopharma.com.
Poster:
A Randomized, Placebo-Controlled Phase 2 Study of ARRY-797 in Patients with Osteoarthritis Pain Refractory to NSAID Treatment Showed Statistically Significant Improvements in WOMAC Pain and in Biomarkers of Bone and Cartilage Degradation
Session:
Late Breaking Abstracts
Date:
Tuesday, November 13, 2012
Time:
9:00 - 11:00 AM Eastern Time
Location:
Walter E. Washington Convention Center - Poster Hall (Hall B)
Array announced in July 2012 that ARRY-797, a non-opioid, met its primary endpoint in a randomized, placebo-controlled and active-controlled (oxycodone ER) Phase 2 clinical trial in 157 osteoarthritis patients suffering from moderate to severe knee pain despite the use of non-steroidal anti-inflammatory drugs (NSAIDs). Patients in all treatment groups continued using NSAIDs throughout the trial. ARRY-797 is a novel, oral, selective p38 inhibitor with a mechanism of action unique from that of currently approved pain medications. Given our internal focus on hematology/oncology, Array is in active discussions with potential partners to maximize the value of this drug.
About Array BioPharma Array BioPharma Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of targeted small-molecule drugs to treat patients afflicted with cancer. Array is evolving into a late-stage development company, with two wholly-owned programs, ARRY-614 and ARRY-520, and three partnered programs, selumetinib (with AstraZeneca), MEK162 (with Novartis), and danoprevir (with InterMune / Roche), having the potential to begin Phase 3 or pivotal trials by the end of calendar year 2013. For more information on Array, please go to www.arraybiopharma.com.