Theravance says that its experimental therapy for chronic constipation met its endpoints for all three doses tested in a mid-stage, 400-patient trial. A total of 61 percent of the patients taking the 50 mg dose of TD-5108 responded with increased spontaneous bowel movements as did 60 percent of the patients take a 15 mg dose and 42 percent taking a 30 mg dose. In the placebo arm, 22 percent of patients responded. No serious adverse effects were recorded and headache, diarrhea, nausea and vomiting were listed as the most common side effects. GlaxoSmithKline has a license option for the therapy that dates back to 2004.
- see the release [1]
- read the AP report [2] on the data
Related Articles:
Theravance declares success in antibiotic trial. Report [3]
Theravance, Astellas ink $65M deal. Report [4]
Links:
[1] http://www.fiercebiotech.com/node/7398
[2] http://www.chron.com/disp/story.mpl/ap/fn/4918911.html
[3] http://www.fiercebiotech.com/story/theravance-declares-success-in-antibiotic-trial/2006-08-23
[4] http://www.fiercebiotech.com/story/theravance-astellas-ink-65m-deal/2005-11-08