| HOME >> BIOLOGY >> TECHNOLOGY |
Darapladib Demonstrates Promise in Phase 2; GSK Confirms Plan to Initiate Phase 3 Development
In September 2008, results of the Integrated Biomarkers and Imaging Study- 2 (IBIS-2) showed that the use of darapladib, in addition to standard of care treatment, prevented expansion of the necrotic core, a region within coronary plaque associated with a high risk of rupture. Preventing expansion of the necrotic core may reduce the risk of recurrent heart attack in patients with coronary heart disease. The results of the Phase 2 study were presented at the 2008 Congress of the European Study of Cardiology and simultaneously published in the American Heart Association's journal, Circulation.
In its third quarter results press release issued October 22, 2008, GSK said, "These data support our belief that Lp-PLA2 inhibition may be an important therapeutic target and we plan to begin Phase 3 clinical studies shortly." Darapladib was discovered by GSK based on HGS technology. HGS will receive a 10% royalty on worldwide sales of darapladib if it is commercialized, and has a 20% co-promotion option in North America and Europe.
Process Development and Manufacturing Alliance with Hospira will Enable HGS to Generate Revenue from Available Manufacturing Capacity
In September 2008, HGS entered into an exclusive agreement with
Hospira, Inc., for manufacturing process development and commercial supply
of select Hospira biopharmaceutical products. In addition to the
partnership with Hospira, HGS entered into a marketing services agreement
with Eden Biodesign Ltd. in August 2008, under which Eden Biodesign will
assist HGS in identifying other clients interested in large-scale
manufacturing and late-stage process development. The Hospira alliance and
similar agreements have the potential to generate $30-60 mi
'/>"/>
| SOURCE Human Genome Sciences, Inc. Copyright©2008 PR Newswire. All rights reserved |