| In Light of Safety Concerns, Abbott’s Briakinumab Faces a Rough Road Ahead in the Psoriasis Drug Market
Based on our Pharmacor advisory service entitled Psoriasis, Decision Resources is offering an exclusive analyst call entitled In Light of Safety Concerns, Abbott’s Briakinumab Faces a Rough Road Ahead in the Psoriasis Drug Market. Because this presentation will feature major updates, it is ONLY available to purchasers of this Pharmacor advisory service.
Please contact us to learn how you can purchase this Pharmacor advisory service and attend the analyst call.
Among the therapies poised to enter the psoriasis drug market in the next few years, Abbott’s briakinumab has the potential to have the greatest impact. If approved, briakinumab would join Centocor Ortho Biotech/Janssen Cilag’s Stelara as a second-in-class interleukin (IL) 12/23 inhibitor and would represent another treatment option for patients with moderate-to-severe psoriasis. Although both Stelara and briakinumab have shown superb efficacy and, as a result, threaten the dominance of the tumor necrosis factor-alpha (TNF-alpha) inhibitors, they suffer from a dearth of long-term safety data and a lack of approval in other indications.
The results of three Phase III clinical trials—a 1,465-patient placebo-controlled study, and two head-to-head trials of briakinumab against etanercept (Amgen/Stiefel/Pfizer/Takeda’s Enbrel)—were reported in detail at the recent American Academy of Dermatology conference and the Third International Congress on Psoriasis. Based on the safety events which emerged from briakinumab’s placebo-controlled Phase III trial, Decision Resources forecasts that briakinumab will fall out of competition for first-line biologic status and be used mainly as later-line therapy in patients refractory to TNF-alpha inhibitors and Stelara.
This 15-minute analyst call, presented by Analyst Iva Holder, Ph.D., will answer the following questions:
- What were the results of the Phase III clinical trials of briakinumab and what are the implications of these new data on Decision Resources’ assumptions and forecast for briakinumab?
- How will these data affect Stelara’s performance in the psoriasis drug market?
- Do the IL-12/23 inhibitors still pose a threat to the dominace of the TNF-alpha inhibitors?
Dr. Holder will conduct a live Q & A session after the presentation.
Registration
In Light of Safety Concerns, Abbott’s Briakinumab Faces a Rough Road Ahead in the Psoriasis Drug Market
September 7, 2010 at 10 a.m. U.S. Eastern Time, 4 p.m. Central European Time (Paris).
To learn how you can purchase this Pharmacor advisory service and attend the analyst call, please contact us using the information below.
Contact Us
In North America — Keith Rourke at 781-993-2656 or krourke@dresources.com
In Europe — Kaj van Langendonck at +32-2-357-06-14 or kvanlangendonck@decisionresources.be
In Japan — Makiko Yoshimoto at +81-3-5401-2615 or makiko@dresources.jp |
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Date & Time
Tuesday, September 7, 2010
10 a.m. U.S. Eastern Time,
4
p.m. Central European Time Duration
15 minutes  |
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Iva Holder, Ph.D. is an analyst in the immune and inflammatory diseases group at Decision Resources. She received her B.A. from Smith College and her Ph.D. from Johns Hopkins University School of Medicine. Following postdoctoral research in the Department of Genetics at Harvard Medical School, she joined Decision Resources, where she is working on reports on irritable bowel syndrome and psoriasis.
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