In IBS-C patients, at least 30% abdominal pain reduction occurred in 70% with linaclotide versus 50% with placebo over 26 weeks.
In plain wordsIn IBS-C patients, linaclotide increased the proportion with reduced abdominal pain versus placebo.
- Peptide
- Linaclotide
- Outcome
- IncreaseAt least 30% abdominal pain reduction
- Study
n = 805
- Comparator
- Placebo
- Outcome group
- Pain · Gastrointestinal
- Studied dose
- 290 μg once daily · oral · 26 weeksAs given in this study (human).
Measurements
- Patients with at least 30% reduction in abdominal pain
- 70%
- linaclotide 290 μg once daily for 26 weeks
- Patients with at least 30% reduction in abdominal pain
- 50%
- placebo for 26 weeks
Source sentences
During 26 weeks of linaclotide administration, a significantly greater percentage of patients (70%) had at least a 30% reduction in abdominal pain compared with patients given placebo (50%).
1 context sentence(design, population, supporting numbers)
We performed a post-hoc analysis of data from a phase III, double-blind, parallel-group study in which 805 patients with IBS-C were randomly assigned to groups given an oral placebo or 290 μg linaclotide once daily for 26 weeks.